Thursday, September 28, 2017

Oyster Mushroom, Natural Source Of Lovastatin


These are natural mushrooms grown by me on my farm in Deming NM.  The spores came from wild mushrooms I collected in Florida, white and pink oysters growing on oak.  These will be both whole and pieces, and can be rehydrated and cooked, or chopped into very small pieces and put into gel  capsules.  The latter is the recommended way to use this as a drug, because cooking always depletes some of the values of anything.  There are also subsidiary conversions when heat is applied to most foods, where undesirable or even harmful elements are literally created.  A good way to finely chop dried herbs is with scissors.

$4.00 per oz

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Here is the wikipedia article on Lovastatin:


Lovastatin
From Wikipedia, the encyclopedia
Clinical data
Trade names     Mevacor
Synonyms     Monacolin K, Mevinolin
AHFS/Drugs.com     Monograph
MedlinePlus     a688006
Pregnancy
category    
   US: X (Contraindicated)
Routes of
administration     Oral
ATC code    
    C10AA02 (WHO)
Legal status
Legal status    
    US: ℞-only
Pharmacokinetic data
Bioavailability     <5%[1]
Protein binding     >98%[1]
Metabolism     Hepatic (CYP3A and CYP2C8 substrate)[1]
Biological half-life     2–5 hours[1]
Excretion     Faeces (83%), urine (10%)[1]
Identifiers
IUPAC name
[show]
CAS Number    
    75330-75-5 Yes
PubChem CID    
    53232
IUPHAR/BPS    
    2739
DrugBank    
    DB00227 Yes
ChemSpider    
    48085 Yes
UNII    
    9LHU78OQFD
KEGG    
    D00359 Yes
ChEBI    
    CHEBI:40303 Yes
ChEMBL    
    CHEMBL503 Yes
ECHA InfoCard     100.115.931
Chemical and physical data
Formula     C24H36O5
Molar mass     404.54 g/mol

Lovastatin (Merck's Mevacor) is a statin drug, used for lowering cholesterol in those with hypercholesterolemia to reduce risk of cardiovascular disease. Lovastatin is a naturally occurring compound found in low concentrations in food such as oyster mushrooms,[2] red yeast rice,[3] and Pu-erh.[4]

Contents

    1 Medical uses
    2 Side effects
        2.1 Contraindications
        2.2 Interactions
    3 Mechanism of action
    4 History
    5 Discovery, biochemistry and biology
        5.1 Biosynthesis using Diels-Alder catalyzed cyclization
        5.2 Total synthesis
        5.3 Stability
    6 Pharmacopoeial information
    7 Brand names
    8 Other applications
    9 See also
    10 References
    11 External links

Medical uses

The primary uses of lovastatin is for the treatment of dyslipidemia and the prevention of cardiovascular disease.[5] It is recommended to be used only after other measures, such as diet, exercise, and weight reduction, have not improved cholesterol levels.[5]
Side effects

Lovastatin is usually well tolerated, with the most common side effects being, in approximately descending order of frequency: creatine phosphokinase elevation, flatulence, abdominal pain, constipation, diarrhoea, muscle aches or pains, nausea, indigestion, weakness, blurred vision, rash, dizziness and muscle cramps.[6] As with all statin drugs, it can rarely cause myopathy, hepatotoxicity (liver damage), dermatomyositis or rhabdomyolysis.[6] This can be life-threatening if not recognised and treated in time, so any unexplained muscle pain or weakness whilst on lovastatin should be promptly mentioned to the prescribing doctor. Other uncommon side effects that should be promptly mentioned to either the prescribing doctor or an emergency medical service include:[7]

    muscle pain, tenderness, or weakness
    lack of energy
    weakness
    fever
    dark colored urine
    jaundice: yellowing of the skin or eyes
    pain in the upper right part of the stomach
    nausea
    unusual bleeding or bruising
    loss of appetite
    flu-like symptoms
    rash
    hives
    itching
    difficulty breathing or swallowing
    swelling of the face, throat, tongue, lips, eyes, hands, feet, ankles, or lower legs
    hoarseness

These less serious side effects should still be reported if they persist or increase in severity:[7]

    constipation
    memory loss or forgetfulness
    confusion

Contraindications

Contraindications, conditions that warrant withholding treatment with lovastatin, include pregnancy, breast feeding, and liver disease. Lovastatin is contraindicated during pregnancy (Pregnancy Category X); it may cause birth defects such as skeletal deformities or learning disabilities. Due to its potential to disrupt infant lipid metabolism, lovastatin should not be taken while breastfeeding.[8] Patients with liver disease should not take lovastatin.[9]
Interactions

As with atorvastatin, simvastatin, and other statin drugs metabolized via CYP3A4, drinking grapefruit juice during lovastatin therapy may increase the risk of side effects. Components of grapefruit juice, the flavonoid naringin, or the furanocoumarin bergamottin inhibit CYP3A4 in vitro,[10] and may account for the in vivo effect of grapefruit juice concentrate decreasing the metabolic clearance of lovastatin, and increasing its plasma concentrations.[11]
Mechanism of action

Lovastatin is an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase), an enzyme that catalyzes the conversion of HMG-CoA to mevalonate.[12] Mevalonate is a required building block for cholesterol biosynthesis and lovastatin interferes with its production by acting as a reversible competitive inhibitor for HMG-CoA, which binds to the HMG-CoA reductase. Lovastatin is a prodrug, an inactive lactone in its native form, the gamma-lactone closed ring form in which it is administered, is hydrolysed in vivo to the β-hydroxy acid open ring form; which is the active form.

Lovastatin and other statins have been studied for their chemopreventive and chemotherapeutic effects. No such effects were seen in the early studies.[13] More recent investigations revealed some chemopreventive and therapeutic effects, for certain types of cancer, especially in combination of statins with other anticancer drugs.[14] It is likely that these effect are mediated by the properties of statins to reduce proteasome activity, leading to an accumulation of cyclin-dependent kinase inhibitors p21 and p27, and to subsequent G1-phase arrest, as seen in cells of different cancer lines.[15][16]
History
Pleurotus ostreatus, the oyster mushroom, naturally contains up to 2.8% lovastatin on a dry weight basis.[17]

Compactin and lovastatin, natural products with a powerful inhibitory effect on HMG-CoA reductase, were discovered in the 1970s, and taken into clinical development as potential drugs for lowering LDL cholesterol.[18][19]

In 1982, some small-scale clinical investigations of lovastatin, a polyketide-derived natural product isolated from Aspergillus terreus, in very high-risk patients were undertaken, in which dramatic reductions in LDL cholesterol were observed, with very few adverse effects. After the additional animal safety studies with lovastatin revealed no toxicity of the type thought to be associated with compactin, clinical studies continued.

Large-scale trials confirmed the effectiveness of lovastatin. Observed tolerability continued to be excellent, and lovastatin was approved by the US FDA in 1987.[20] It was the first statin approved by the FDA.[21]

Lovastatin is also naturally produced by certain higher fungi, such as Pleurotus ostreatus (oyster mushroom) and closely related Pleurotus spp.[22] Research into the effect of oyster mushroom and its extracts on the cholesterol levels of laboratory animals has been extensive,[23][24][22][25][26][27][28][29][30][31][32][33] although the effect has been demonstrated in a very limited number of human subjects.[34]

In 1998, the FDA placed a ban on the sale of dietary supplements derived from red yeast rice, which naturally contains lovastatin, arguing that products containing prescription agents require drug approval.[35] Judge Dale A. Kimball of the United States District Court for the District of Utah, granted a motion by Cholestin's manufacturer, Pharmanex, that the agency's ban was illegal under the 1994 Dietary Supplement Health and Education Act because the product was marketed as a dietary supplement, not a drug.[36]
Discovery, biochemistry and biology
A ball-and-stick model of lovastatin

An elevated concentration of plasma cholesterol, especially low-density lipoprotein (LDL) cholesterol, is now generally accepted as a major risk factor for the development of coronary heart disease.[37] The objective is to decrease excess levels of cholesterol to an amount consistent with maintenance of normal body function. Cholesterol is biosynthesized in a series of more than 25 separate enzymatic reactions that initially involves three successive condensations of acetyl-CoA units to form the six-carbon compound 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA). This is reduced to mevalonate and then converted in a series of reactions to the isoprenes that are building-blocks of squalene, the immediate precursor to sterols, which cyclizes to lanosterol (a methylated sterol) and further metabolized to cholesterol. A number of early attempts to block the synthesis of cholesterol resulted in agents that inhibited late in the biosynthetic pathway between lanosterol and cholesterol. A major rate-limiting step in the pathway is at the level of the microsomal enzyme that catalyzes the conversion of HMG CoA to mevalonic acid, and that has been considered to be a prime target for pharmacologic intervention for several years.[12]

HMG CoA reductase occurs early in the biosynthetic pathway and is among the first committed steps to cholesterol formulation. Inhibition of this enzyme could lead to accumulation of HMG CoA, a water-soluble intermediate that is, then, capable of being readily metabolized to simpler molecules. This inhibition of reductase would lead to accumulation of lipophylic intermediates with a formal sterol ring.

Lovastatin was the first specific inhibitor of HMG CoA reductase to receive approval for the treatment of hypercholesterolemia. The first breakthrough in efforts to find a potent, specific, competitive inhibitor of HMG CoA reductase occurred in 1976, when Endo et al. reported the discovery of mevastatin, a highly functionalized fungal metabolite, isolated from cultures of Penicillium citrium.[38] Mevastatin was demonstrated to be an unusually potent inhibitor of the target enzyme and of cholesterol biosynthesis. Subsequent to the first reports describing mevastatin, efforts were initiated to search for other naturally occurring inhibitors of HMG CoA reductase. This led to the discovery of a novel fungal metabolite – lovastatin. The structure of lovastatin was determined to be different from that of mevastatin by the presence of a six alphamethyl group in the hexahydronaphthalene ring.

Key points from the study of the biosynthesis of lovastatin:

    Lovastatin is composed of two polyketide chains derived from acetate, two and four carbons long, coupled in head-to-tail fashion.
    The six alphamethyl group and the methyl group on the four-carbon side-chain are derived from the methyl group of methionine.
    The six alphamethyl group is added before closure of the rings.

This implies that lovastatin is a unique compound synthesized by A. terreus and that mevastatin is not an intermediate in its formation.
Cholesterol biosynthetic pathway
HMG CoA reductase reaction
Biosynthesis using Diels-Alder catalyzed cyclization

In vitro formation of a triketide lactone using a genetically modified protein derived from 6-deoxyerythronolide B synthase has been demonstrated. Witter and Vederas observed, "the stereochemistry of the molecule supports the intriguing idea that an enzyme-catalyzed Diels-Alder reaction may occur during assembly of the polyketide chain. It, thus, appears that biological Diels-Alder reactions may be triggered by generation of reactive triene systems on an enzyme surface."[39]
Biosynthesis using Diels-Alder catalyzed cyclization
Biosynthesis using broadly specific acyltransferase
Total synthesis

A major bulk of work in the synthesis of lovastatin was done by M. Hirama in the 1980s.[40] [41] Hirama synthesized compactin and used one of the intermediates to follow a different path to get to lovastatin. The synthetic sequence is shown in the schemes below. The γ-lactone was synthesized using Yamada methodology starting with glutamic acid. Lactone opening was done using lithium methoxide in methanol and then silylation to give a separable mixture of the starting lactone and the silyl ether. The silyl ether on hydrogenolysis followed by Collins oxidation gave the aldehyde. Stereoselective preparation of (E,E)-diene was accomplished by addition of trans-crotyl phenyl sulfone anion, followed by quenching with Ac2O and subsequent reductive elimination of sulfone acetate. Condensation of this with lithium anion of dimethyl methylphosphonate gave compound 1. Compound 2 was synthesized as shown in the scheme in the synthetic procedure. Compounds 1 and 2 were then combined together using 1.3 eq sodium hydride in THF followed by reflux in chlorobenzene for 82 hr under nitrogen to get the enone 3.

Simple organic reactions were used to get to lovastatin as shown in the scheme.
Synthesis of compounds 1 and 2
Complete lovastatin synthesis
Stability

Due to its oxidative instability it is possible to add antioxidants to improve stability.[42]
Pharmacopoeial information

Lovastatin tablets are preserved when stored in well-closed, light-resistant containers in a cool place or at controlled room temperature.

Lovastatin tablets are tested for dissolution and assay as per the USP.

Limit for dissolution – Not less than 80% (Q) of the labeled amount of lovastatin is dissolved in 30 minutes.

Limit for assay – Each tablet contains not less than 90% and not more than 110% of the labeled amount of lovastatin, tested by HPLC analysis.
Brand names

    Mevacor
    Advicor (as a combination with niacin)
    Altocor
    Altoprev

Other applications

In plant physiology, lovastatin has occasionally been used as inhibitor of cytokinin biosynthesis.[43]
See also

    Medicinal fungi

References

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Gunde-Cimerman N; Cimerman A. (Mar 1995). "Pleurotus fruiting bodies contain the inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase-lovastatin.". Exp Mycol. 19 (1): 1–6. PMID 7614366. doi:10.1006/emyc.1995.1001.
Liu J, Zhang J, Shi Y, Grimsgaard S, Alraek T, Fønnebø V (2006). "Chinese red yeast rice (Monascus purpureus) for primary hyperlipidemia: a meta-analysis of randomized controlled trials". Chin Med. 1 (1): 4. PMC 1761143 Freely accessible. PMID 17302963. doi:10.1186/1749-8546-1-4.
Zhao ZJ, Pan YZ, Liu QJ, Li XH (2013). "Exposure assessment of lovastatin in Pu-erh tea". International Journal of Food Microbiology. 164 (1): 26–31. PMID 23587710. doi:10.1016/j.ijfoodmicro.2013.03.018.
"Lovastatin". The American Society of Health-System Pharmacists. Retrieved 3 April 2011.
"Mevacor, Altoprev (lovastatin) dosing, indications, interactions, adverse effects, and more". Medscape Reference. WebMD. Retrieved 17 March 2014.
"Lovastatin". MedlinePlus. U.S. National Library of Medicine. 15 June 2012. Retrieved 1 December 2012.
"Lovastatin". LactMed. U.S. National Library of Medicine. Retrieved 1 December 2012.
Stöppler, Melissa. "Mevacor Side Effects Center". RxList. Retrieved 1 December 2012.
David G. Bailey, J. Malcolm, O. Arnold, J. David Spence (1998). "Grapefruit juice-drug interactions". Br J Clin Pharmacol 46 (2): 101–110. doi:10.1046/j.1365-2125.1998.00764.x. PMC 1873672. PMID 9723817.
Kantola T, Kivistö KT, Neuvonen PJ (Apr 1998). "Grapefruit juice greatly increases serum concentrations of lovastatin and lovastatin acid". Clin Pharmacol Ther. 63 (4): 397–402. PMID 9585793. doi:10.1016/S0009-9236(98)90034-0.
Alberts AW (1998). "Discovery, biochemistry and biology of lovastatin". The American Journal of Cardiology. 62 (15): 10J–15J. PMID 3055919. doi:10.1016/0002-9149(88)90002-1.
Katz MS (2005). "Therapy insight: Potential of statins for cancer chemoprevention and therapy". Nature Clinical Practice Oncology. 2 (2): 82–9. PMID 16264880. doi:10.1038/ncponc0097.
Chae YK, Yousaf M, Malecek MK, Carneiro B, Chandra S, Kaplan J, Kalyan A, Sassano A, Platanias LC, Giles F. (2015) Statins as anti-cancer therapy; Can we translate preclinical and epidemiologic data into clinical benefit? Discov Med. Dec;20(112):413-27. PMID 26760985.
Jakóbisiak M, Bruno S, Skierski J, Darzynkiewicz Z. (1991) The cell cycle specific effects of lovastatin. Proc Natl Acad Sci USA 88:3628-3632. PMID 1673788 PMC 51505
Rao S, Porter DC, Chen X, Herliczek T, Lowe M, Keyomarsi K (July 1999). "Lovastatin-mediated G1 arrest is through inhibition of the proteasome, independent of hydroxymethyl glutaryl-CoA reductase". Proc. Natl. Acad. Sci. U.S.A. 96 (14): 7797–802. PMC 22141 Freely accessible. PMID 10393901. doi:10.1073/pnas.96.14.7797.
Alarcón J, Aguila S, Arancibia-Avila P, Fuentes O, Zamorano-Ponce E, Hernández M (Jan–Feb 2003). "Production and purification of statins from Pleurotus ostreatus (Basidiomycetes) strains". Z Naturforsch C. 58 (1–2): 62–4. PMID 12622228. doi:10.1515/znc-2003-1-211.
Vederas JC, Moore RN, Bigam G, Chan KJ (1985). "Biosynthesis of the hypocholesterolemic agent mevinolin by Aspergillus terreus. Determination of the origin of carbon, hydrogen and oxygen by 13C NMR and mass spectrometry". J Am Chem Soc. 107 (12): 3694–701. doi:10.1021/ja00298a046.
Alberts AW, Chen J, Kuron G, Hunt V, Huff J, Hoffman C, Rothrock J, Lopez M, Joshua H, Harris E, Patchett A, Monaghan R, Currie S, Stapley E, Albers-Schonberg G, Hensens O, Hirshfield J, Hoogsteen K, Liesch J, Springer J (July 1980). "Mevinolin: a highly potent competitive inhibitor of hydroxymethlglutaryl-coenzyme A reductase and a cholesterol-lowering agent". Proc Natl Acad Sci U S A. 77 (7): 3957–61. PMC 349746 Freely accessible. PMID 6933445. doi:10.1073/pnas.77.7.3957.
FDA Orange Book Detail for application N019643 showing approval for 20 mg tablets on Aug 31, 1987 and 40 mg tablets on Dec 14, 1988
Endo, Akira (Oct 2004). "The origin of the statins". Atheroscler. Suppl. 5 (3): 125–30. PMID 15531285. doi:10.1016/j.atherosclerosissup.2004.08.033.
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Bobek P, Galbavý S (October 1999). "Hypocholesterolemic and antiatherogenic effect of oyster mushroom (Pleurotus ostreatus) in rabbits". Nahrung. 43 (5): 339–42. PMID 10555301. doi:10.1002/(SICI)1521-3803(19991001)43:5<339::AID-FOOD339>3.0.CO;2-5.
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Bajaj M, Vadhera S, Brar AP, Soni GL (October 1997). "Role of oyster mushroom (Pleurotus florida) as hypocholesterolemic/antiatherogenic agent". Indian J. Exp. Biol. 35 (10): 1070–5. PMID 9475042.
Bobek P, Ozdín L, Kuniak L, Hromadová M (March 1997). "[Regulation of cholesterol metabolism with dietary addition of oyster mushrooms (Pleurotus ostreatus) in rats with hypercholesterolemia]". Cas. Lek. Cesk. (in Slovak). 136 (6): 186–90. PMID 9221192.
Bobek P, Ozdín L, Kuniak L (August 1996). "Effect of oyster mushroom (Pleurotus Ostreatus) and its ethanolic extract in diet on absorption and turnover of cholesterol in hypercholesterolemic rat". Nahrung. 40 (4): 222–4. PMID 8810086. doi:10.1002/food.19960400413.
Bobek P, Ozdín O, Mikus M (1995). "Dietary oyster mushroom (Pleurotus ostreatus) accelerates plasma cholesterol turnover in hypercholesterolaemic rat". Physiol Res. 44 (5): 287–91. PMID 8869262.
Bobek P, Ozdin L, Kuniak L (1995). "The effect of oyster mushroom (Pleurotus ostreatus), its ethanolic extract and extraction residues on cholesterol levels in serum, lipoproteins and liver of rat". Nahrung. 39 (1): 98–9. PMID 7898579. doi:10.1002/food.19950390113.
Bobek P, Ozdin L, Kuniak L (March 1994). "Mechanism of hypocholesterolemic effect of oyster mushroom (Pleurotus ostreatus) in rats: reduction of cholesterol absorption and increase of plasma cholesterol removal". Z Ernahrungswiss. 33 (1): 44–50. PMID 8197787. doi:10.1007/BF01610577.
Chorváthová V, Bobek P, Ginter E, Klvanová J (1993). "Effect of the oyster fungus on glycaemia and cholesterolaemia in rats with insulin-dependent diabetes". Physiol Res. 42 (3): 175–9. PMID 8218150.
Bobek P, Ginter E, Jurcovicová M, Kuniak L (1991). "Cholesterol-lowering effect of the mushroom Pleurotus ostreatus in hereditary hypercholesterolemic rats". Ann. Nutr. Metab. 35 (4): 191–5. PMID 1897899. doi:10.1159/000177644.
Khatun K, Mahtab H, Khanam PA, Sayeed MA, Khan KA (January 2007). "Oyster mushroom reduced blood glucose and cholesterol in diabetic subjects". Mymensingh Med J. 16 (1): 94–9. PMID 17344789. doi:10.3329/mmj.v16i1.261.
"FDA bans red yeast rice product" by Michael McCarthy, The Lancet, Volume 351, Issue 9116, Page 1637, 30 May 1998
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Endo, Akira; Kuroda M.; Tsujita Y. (December 1976). "ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogenesis produced by Penicillium citrinium". Journal of Antibiotics (Tokyo). 29 (12): 1346–8. PMID 1010803. doi:10.7164/antibiotics.29.1346.
Witter, DJ; Vederas, JC (1996). "Putative Diels-Alder catalyzed cyclization during the biosynthesis of lovastatin". J Org Chem. 61 (8): 2613–23. PMID 11667090. doi:10.1021/jo952117p.
Hirama M, Vet M (1982). "A chiral total synthesis of compactin". J. Am. Chem. Soc. 104 (15): 4251. doi:10.1021/ja00379a037.
Hirama M, Iwashita; Iwashita, Mitsuko (1983). "Synthesis of (+)-Mevinolin starting from Naturally occurring building blocks and using an asymmetry inducing reaction". Tetrahedron Lett. 24 (17): 1811–1812. doi:10.1016/S0040-4039(00)81777-3.
Javernik S, Kreft S, Strukelj B, Vrecer F (2001). "Oxidation of lovastatin in the solid state and its stabilization with natural antioxidants". Die Pharmazie. 56 (9): 738–40. PMID 11593996.

    Hartig K, Beck E (2005). "Assessment of lovastatin application as tool in probing cytokinin-mediated cell cycle regulation". Physiologia Plantarum. 125 (2): 260–267. doi:10.1111/j.1399-3054.2005.00556.x.

Bloodroot, Blood Root, Sanguinaria canidensis

This plant saved my life.  I was anthraxed by minions of the bush crime family in 2002, when I went to investigate jeb "the mutt" bush right after 911 in Florida.  Before finding bloodroot I had four surgeries and the idiot money doctors of the amerikkkan police state were getting ready to cut off my right arm.  Those fools all have their heads up their wallets, the toads.  I got with Ingrid at cancersalves.com, and bought her book about cancer salves.  I then obtained the bloodroot poultice, and used it after my fourth surgery.  All these surgeries caused the growth to come back bigger and stronger each time, because it was basically misdiagnosed by the idiot children of the inbred AMA. 

This substance (bloodroot, sanguinaria canadensis) is known as an escharotic.  It made my massive wound scab over and heal, after three years of intense suffering which was highlighted buy this things never ending growth as it ate me alive, and its constant weeping of fluids which kept it from healing.  Nothing else I tried even came close to working, and I tried a lot of things, because I could easily sense that the doctors were either inept or complicit or both.  Ridiculous zionists.

Since then I have used bloodroot all over my body to take of lesions, warts,and other growths caused by uv or whatever. I take it four times a year internally, though I do not recommend that for most users.  Do your homework, and take resonsibiklity for your own health.  Doctors can help with advice and drugs, but most of them see hundreds of patients, and they do not have the time or intellectual wherewithal to really care about all those people.  They do care about their money a lot though.

A lot of times bloodroot is mixed with other herbs.  All the recipes, even the Balm Of Gilead, are in Ingrids book, and there is a link to that below the wiki article on this plant,though it leaves a lot to bve desired and is fill with special interest misinformation.  Most government purveyed or college purveyed info today is all special interest garbage, fyi.  The wiki article says that bloodroot harms normal tissue, but I have never had that happen.  As always be careful with any treatment, and don't trust anything or anyone until you see it for yourself.

Bloodroot is the plant that woke me up to the idea that we have been through all this before, because we suffer what is called Periodic Cataclysm, a by-product of our traverse through space, and the subsequent collisions with clouds of debris that happen across our path.  Sometime in the past I think we put all our best drugs in the plants, as is being done again today with genetic sciences, although our efforts today are strictly infantile compared to what came before. 

I believe that all these plants being so beneficial is not an accident, and most good pharmaceuticals are plant derivatives too, if you think about it.  We were really something once, but each time we fall we become a little more devo, a little more retarded in our growth and thinking.   A little more abused. This is plainly evident. 

Sanguinaria canadensis is a true longevity substance.  Life spans of 150-200 years are entirely possible, if we can discoverand employ all the old drugs that are hidden in the plants, created by us before we became so devo.

The plant induces fever.  Even the egyptians knew that some high fevers were the bodies way of killing off cancers.  In 1915 a doctor did a study of records to try to determine why some cancer patients survived after surgery, while others did not.  Without exception he found that all survivors of cancer surgeries had developed high fevers after surgery.  The ones who did not develop fevers after their surgeries died.  True story. Get Ingrids book, its all there.

To treat skin lesions with this bloodroot powder I am offering here, which is #1 grade and very potent, a poultice/paste is made with distilled water and applied only to the top of the growth.  It must remain on the growth for 24 hours, then it can be washed off.  In about a month the lesion will fall off, sometimes it leaves a hole because the roots of these things go deep on occasion.  I only had to apply the poultice twice in one instance, and it was a bad one.  It did not look bad from the surface, but the root went almost 1/2" deep.  It may have been basal cell carcinoma.  

If you want to be more thorough, keep the treated lesion covered with a band aid and vaseline while the chemical surgery is working, and when the lesion finally removes itself after 6 or so weeks any root hole will be filled with new pink flesh.  That is the way Ingrids book instructs, though my lifestyle is much too active for that.  I remove the lesion as soon as it is ready to fall out, then I let the hole scab over in the open air, and then I have a scar.  oh well. 

As for cancer in general, this has become the greatest treasure chest EVER for the ghouls and half wits of the AMA.  They attack us through our food to keep their little profit machine running.  The best thing you can do to stop cancer is stop eating all sugar.  Most everything that eats people is after the sugar we ingest.  Once you try to stop eating sugar, except for fruits, you will see that we are attacked by our own people because there is sugar in almost EVERYTHING, and some very harmful types too.  Wake up.

 At this time I am not growing this myself.


Here is the wiki article on Sanguinaria canidensis:

https://en.wikipedia.org/wiki/Sanguinaria

Buy Ingrids Book Here:

http://www.cancersalves.com/publications/book.html

Saint Johns Wort

A lot of people use this plant to combat anxiety/depression.  I have very little experience with this myself, except that I took a course of gel caps containing St. Johyns Wort because I had read it was effective in treating sciatica.  It did help, and there are many testimonies on the net and elsewhere for you to read concerning this plant material.  At this time I am not growing this myself.  The article from Wikipedia below is a good one.


Hypericum perforatum
From Wikipedia, the free encyclopedia
"St John's wort" redirects here. For other uses, see St John's wort (disambiguation).
Hypericum perforatum
Saint John's wort flowers.jpg
Scientific classification
Kingdom:     Plantae
(unranked):     Angiosperms
(unranked):     Eudicots
(unranked):     Rosids
Order:     Malpighiales
Family:     Hypericaceae
Genus:     Hypericum
Species:     H. perforatum
Binomial name
Hypericum perforatum
L.

Hypericum perforatum, known as perforate St John's-wort,[1] common Saint John's wort and St John's wort,[note 1] is a flowering plant in the family Hypericaceae. The common name "St John's wort" may be used to refer to any species of the genus Hypericum. Therefore, Hypericum perforatum is sometimes called "common St John's wort" or "perforate St John's wort" in order to differentiate it. It is a medicinal herb with antidepressant activity and potent anti-inflammatory properties as an arachidonate 5-lipoxygenase inhibitor and COX-1 inhibitor.[3][4][5]
Contents

    1 Botanical description
    2 Ecology
        2.1 Invasive species
    3 Medical uses
        3.1 Major depressive disorder
    4 Side effects
    5 Interactions
        5.1 Pharmacokinetic
        5.2 Pharmacodynamic
    6 Mechanism of action
    7 Livestock
        7.1 Poisoning
    8 Chemistry
        8.1 Detection in body fluids
        8.2 Chemical constituents
    9 Research
    10 See also
    11 Notes
    12 References
    13 Further reading
    14 External links

Botanical description
Translucent dots of glandular tissue on the leaves

Hypericum perforatum is native to parts of Europe and Asia[6] but has spread to temperate regions worldwide as a cosmopolitan invasive weed.

The common name "St John's wort" comes from its traditional flowering and harvesting on St John's Day, 24 June. The genus name Hypericum is derived from the Greek words hyper (above) and eikon (picture), in reference to the tradition of hanging plants over religious icons in the home during St John's Day, to ward off evil.

Perforate St John's wort is a herbaceous perennial plant with extensive, creeping rhizomes. Its stems are erect, branched in the upper section, and can grow to 1 m high. It has opposite, stalkless, narrow, oblong leaves that are 1–2 cm long.[7]:176 The leaves are yellow-green in color, with scattered translucent dots of glandular tissue.[8] The dots are conspicuous when held up to the light, giving the leaves the 'perforated' appearance to which the plant's Latin name refers. The flowers measure up to 2.5 cm across, have five petals, and are colored bright yellow with conspicuous black dots.[9]:339 The flowers appear in broad cymes at the ends of the upper branches, between late spring and early to mid summer. The sepals are pointed, with black glandular dots. There are many stamens, which are united at the base into three bundles. The pollen grains are ellipsoidal.[2]

When flower buds (not the flowers themselves) or seed pods are crushed, a reddish/purple liquid is produced.[10]
Ecology
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St John's wort reproduces both vegetatively and sexually. It thrives in areas with either a winter- or summer-dominant rainfall pattern; however, distribution is restricted by temperatures too low for seed germination or seedling survival. Altitudes greater than 1500 m, rainfall less than 500 mm, and a daily mean temperature greater than 24 °C are considered limiting thresholds.[who?] Depending on environmental and climatic conditions, and rosette age, St John's wort will alter growth form and habit to promote survival. Summer rains are particularly effective in allowing the plant to grow vegetatively, following defoliation by insects or grazing.

The seeds can persist for decades in the soil seed bank, germinating following disturbance.[11]
Invasive species

Although Hypericum perforatum is grown commercially in some regions of south east Europe, it is listed as a noxious weed in more than twenty countries and has introduced populations in South and North America, India, New Zealand, Australia, and South Africa.[11] In pastures, St John's wort acts as both a toxic and invasive weed. It replaces native plant communities and forage vegetation to the extent of making productive land nonviable[12] or becoming an invasive species in natural habitats and ecosystems. Ingestion by livestock such as horses, sheep, and cattle can cause photosensitization, central nervous system depression, spontaneous abortion or death.[12][13] Effective herbicides for control of Hypericum include 2,4-D, picloram, and glyphosate. In western North America three beetles Chrysolina quadrigemina, Chrysolina hyperici and Agrilus hyperici have been introduced as biocontrol agents.[14]

    Full plant

    Seedlings

    Fruit

    Blossom

Medical uses

Common St. John's-wort has long been used in herbalism. It was known to have medical properties in Classical Antiquity and was a standard component of theriacs, from the Mithridate of Aulus Cornelius Celsus' De Medicina (ca. 30 CE) to the Venice treacle of d'Amsterdammer Apotheek in 1686. Folk usages included oily extract ("St. John's oil") and Hypericum snaps.[15]

Hypericum perforatum is the most potent species and it is today grown commercially for use in herbalism and medicine.[16]

Two main compounds of interest have been studied in more detail: hyperforin and hypericin. As psychiatric medication, it is usually taken as pills, or as tea. Standardised preparations are available, and research has mainly studied alcoholic extracts and isolated compounds. What research data exists supports a noticeable effect in many cases of light and medium depression,[17] but no significant improvement of severe depression and OCD. Two authors of the study are employees at the alternative pharmaceutical company Dr. Willmar Schwabe Pharmaceuticals, which represents a significant conflicting interest.

The red, oily extract of H. perforatum may help heal wounds.[18][19] Both hypericin and hyperforin are reported to have antibiotic properties.[20] Justifying this view with the then-current doctrine of signatures, herbalist William Coles (1626–1662)[21] wrote in the 17th century that:

    "The little holes where of the leaves of Saint Johns wort are full, doe resemble all the pores of the skin and therefore it is profitable for all hurts and wounds that can happen thereunto."

Hypericum perforatum may also be capable of reducing the physical signs of opiate withdrawal.[22]

Hypericum extract, by inducing both the CYP3A4 and the P-glycoprotein (P-gp), can reduce the plasma concentrations of different antineoplastic agents such as imatinib, irinotecan and docetaxel, thus reducing the clinical efficacy of these drugs.[23]
Major depressive disorder

Some studies have supported the efficacy of St John's wort as a treatment for depression in humans, but have not concluded it as a replacement for more studied treatments, and proper medical consultation.[24][5][25] A 2015 meta-analysis review concluded that it has superior efficacy to placebo in treating depression; is as effective as standard antidepressant pharmaceuticals for treating depression; and has fewer adverse effects than other antidepressants. The authors concluded that it is difficult to assign a place for St. John's wort in the treatment of depression owing to limitations in the available evidence base, including large variations in efficacy seen in trials performed in German-speaking relative to other countries.[26] It is proposed that the mechanism of action of St. John's wort is due to the inhibition of reuptake of certain neurotransmitters.[2]

A 2008 Cochrane review of 29 clinical trials concluded that it was superior to placebo in patients with major depression, as effective as standard antidepressants and had fewer side-effects.[27] According to the National Center for Complementary and Integrative Health (NCCIH) of the National Institutes of Health, it "may help some types of depression, though the evidence is not definitive"; can limit the efficacy of prescription medicines; and psychosis can occur as a rare side effect. The NCCIH notes that combining St John's wort with certain prescription antidepressants can lead to a "potentially life-threatening increase of serotonin", a brain chemical targeted by antidepressants.[28] A 2016 review came to the same conclusions as the 2008 Cochrane review, but noted that the quality of evidence in regards to both effectiveness and incidence of adverse effects was reduced relative to that for conventional antidepressants.[29]

In Germany, St. John's wort is sometimes prescribed for mild to moderate depression, especially in children and adolescents.[30][31]
Side effects

St John's wort is generally well tolerated, with an adverse effect profile similar to placebo.[32] Commonly reported adverse effects include gastrointestinal symptoms (nausea, abdominal pain, loss of appetite, and diarrhea), dizziness, confusion, fatigue, sedation, dry mouth, restlessness, and headache.[33][34][35] The organ systems associated with adverse drug reactions to St John's wort and fluoxetine (an SSRI) have a similar incidence profile;[36] most of these reactions involve the central nervous system.[36] St John's wort also decreases the levels of estrogens, such as estradiol, by speeding up its metabolism, and should not be taken by women on contraceptive pills as it upregulates the CYP3A4 cytochrome of the P450 system in the liver.[37]

St John's wort may rarely cause photosensitivity. This can lead to visual sensitivity to light and to sunburns in situations that would not normally cause them.[32]

St John's wort is associated with aggravating psychosis in people who have schizophrenia.[38]
Interactions

St. John's wort has interactions with medications such as SSRI antidepressants, warfarin, and birth control. Combining both St John's wort and SSRI antidepressants could lead to increased serotonin levels causing serotonin syndrome.[39] It should not be taken with the heart medication, ranolazine.[40] Combining estrogen containing oral contraceptives with St John's wort can lead to decreased efficacy of the contraceptive and eventually unplanned pregnancies.[41] St. John's wort has been known to decrease the blood concentrations of immunosuppressants (cyclosporine & tacrolimus), sedatives (midazolam & alprazolam), anticoagulants (phenprocoumon), chemotherapy drugs (irinotecan) and other medications.[42] These are just a few of the drug interactions that St John's wort possesses. It is also known to decrease the efficacy of HIV medications, cholesterol medications, as well as transplant medications.[43]

Consumption of St. John's wort is discouraged for those with bipolar disorder. There is concern that people with bipolar depression taking St. John's wort may be at a higher risk for mania.[44]
Pharmacokinetic

St John's wort has been shown to cause multiple drug interactions through induction of the cytochrome P450 enzymes CYP3A4 and CYP1A2. This drug-metabolizing enzyme induction results in the increased metabolism of certain drugs, leading to decreased plasma concentration and potential clinical effect.[45] The principal constituents thought to be responsible are hyperforin and amentoflavone. There is strong evidence that the mechanism of action of these interactions is activation of the pregnane X receptor.[46]

St John's wort has also been shown to cause drug interactions through the induction of the P-glycoprotein efflux transporter. Increased P-glycoprotein expression results in decreased absorption and increased clearance of certain drugs, leading to lower plasma concentrations and impaired clinical efficacy.[47]
Examples of drugs whose effectiveness may be reduced by St. John's wort Class     Drugs
Antiretrovirals     Non-nucleoside reverse transcriptase inhibitors, protease inhibitors
Benzodiazepines     Alprazolam, midazolam
Hormonal contraception     Combined oral contraceptives
Immunosuppressants     Calcineurin inhibitors, cyclosporine, tacrolimus
Antiarrhythmics     Amiodarone, flecainide, mexiletine
Beta-blockers     Metoprolol, carvedilol
Calcium channel blockers     Verapamil, diltiazem, amlodipine
Statins (cholesterol-reducing medications)     Lovastatin, simvastatin, atorvastatin
Others     Digoxin, methadone, omeprazole, phenobarbital, theophylline, warfarin, levodopa, buprenorphine, irinotecan
Reference: Rossi, 2005; Micromedex

For a complete list, see CYP3A4 ligands and CYP2C9 ligands.
Pharmacodynamic

In combination with other drugs that may elevate 5-HT (serotonin) levels in the central nervous system (CNS), St John's wort may contribute to serotonin syndrome, a potentially life-threatening adverse drug reaction.[48]
Drugs that may contribute to serotonin syndrome with St John's wort Class     Drugs
Antidepressants     MAOIs, TCAs, SSRIs, SNRIs, mirtazapine
Opioids     Tramadol, pethidine (meperidine), levorphanol
CNS stimulants     Phentermine, diethylpropion, amphetamines, sibutramine, cocaine
5-HT1 agonists     Triptans
Psychedelic drugs     Methylenedioxymethamphetamine (MDMA), LSD, dimethyltryptamine (DMT), MDA, 6-APB
Others     Selegiline, tryptophan, buspirone, lithium, linezolid, 5-HTP, dextromethorphan
Reference:[48]
Mechanism of action

St. John's wort, similarly to other herbs, contains a whole host of different chemical constituents that may be pertinent to its therapeutic effects.[49] Hyperforin and adhyperforin, two phloroglucinol constituents of St John's wort, are TRPC6 receptor agonists and, consequently, they induce noncompetitive reuptake inhibition of monoamines (specifically, dopamine, norepinephrine, and serotonin), GABA, and glutamate when they activate this ion channel.[25][50][51] In humans, the active ingredient hyperforin is also an inhibitor of PTGS1, arachidonate 5-lipoxygenase, SLCO1B1 and an inducer of cMOAT.[50][51][52] Hyperforin is also a anti-inflammatory compound with anti-angiogenic, antibiotic, and neurotrophic properties.[50][51][52] Hyperforin also has an antagonistic effect on NMDA receptors, a type of glutamate receptor.[51] Moreover, St John's wort is known to downregulate the β1 adrenoceptor and upregulate postsynaptic 5-HT1A and 5-HT2A receptors, both of which are a type of serotonin receptor.[25] Other compounds may also play a role in St John's wort's antidepressant effects. Such compounds include: oligomeric procyanidines, flavonoids (quercetin), hypericin, and pseudohypericin.[25][53][54][55]
Comparison of selected active chemical constituents of Hypericum perforatum[49][56]

[show]
Livestock
Poisoning

In large doses, St John's wort is poisonous to grazing livestock (cattle, sheep, goats, horses).[12] Behavioural signs of poisoning are general restlessness and skin irritation. Restlessness is often indicated by pawing of the ground, headshaking, head rubbing, and occasional hindlimb weakness with knuckling over, panting, confusion, and depression. Mania and hyperactivity may also result, including running in circles until exhausted. Observations of thick wort infestations by Australian graziers include the appearance of circular patches giving hillsides a 'crop circle' appearance, it is presumed, from this phenomenon. Animals typically seek shade and have reduced appetite. Hypersensitivity to water has been noted, and convulsions may occur following a knock to the head. Although general aversion to water is noted, some may seek water for relief.

Severe skin irritation is physically apparent, with reddening of non-pigmented and unprotected areas. This subsequently leads to itch and rubbing, followed by further inflammation, exudation, and scab formation. Lesions and inflammation that occur are said to resemble the conditions seen in foot and mouth disease. Sheep have been observed to have face swelling, dermatitis, and wool falling off due to rubbing. Lactating animals may cease or have reduced milk production; pregnant animals may abort. Lesions on udders are often apparent. Horses may show signs of anorexia, depression (with a comatose state), dilated pupils, and injected conjunctiva.
Diagnosis

Increased respiration and heart rate is typically observed while one of the early signs of St John's wort poisoning is an abnormal increase in body temperature. Affected animals will lose weight, or fail to gain weight; young animals are more affected than old animals. In severe cases death may occur, as a direct result of starvation, or because of secondary disease or septicaemia of lesions. Some affected animals may accidentally drown. Poor performance of suckling lambs (pigmented and non-pigmented) has been noted, suggesting a reduction in the milk production, or the transmission of a toxin in the milk.
Photosensitisation

Most clinical signs in animals are caused by photosensitisation.[105] Plants may induce either primary or secondary photosensitisation:

    primary photosensitisation directly from chemicals contained in ingested plants
    secondary photosensitisation from plant-associated damage to the liver.

Araya and Ford (1981) explored changes in liver function and concluded there was no evidence of Hypericum-related effect on the excretory capacity of the liver, or any interference was minimal and temporary. However, evidence of liver damage in blood plasma has been found at high and long rates of dosage.

Photosensitisation causes skin inflammation by a mechanism involving a pigment or photodynamic compound, which when activated by a certain wavelength of light leads to oxidation reactions in vivo. This leads to lesions of tissue, particularly noticeable on and around parts of skin exposed to light. Lightly covered or poorly pigmented areas are most conspicuous. Removal of affected animals from sunlight results in reduced symptoms of poisoning.
Chemistry
Detection in body fluids

Hypericin, pseudohypericin, and hyperforin may be quantitated in plasma as confirmation of usage and to estimate the dosage. These three active substituents have plasma elimination half-lives within a range of 15–60 hours in humans. None of the three has been detected in urine specimens.[106]
Chemical constituents
Chemical structure of hypericin

The plant contains the following:[49][57]

    Flavonoids (e.g. epigallocatechin, rutin, hyperoside, isoquercetin, quercitrin, quercetin, amentoflavone, biapigenin, astilbin, myricetin, miquelianin, kaempferol, luteolin)
    Phenolic acids (e.g. chlorogenic acid, caffeic acid, p-coumaric acid, ferulic acid, p-hydroxybenzoic acid, vanillic acid)
    Naphthodianthrones (e.g. hypericin, pseudohypericin, protohypericin, protopseudohypericin)
    Phloroglucinols (e.g. hyperforin, adhyperforin)
    Tannins (unspecified, proanthocyanidins reported)
    Volatile oils (e.g. 2-methyloctane, nonane, 2-methyldecane, undecane, α-pinene, β-pinene, α-terpineol, geraniol, myrcene, limonene, caryophyllene, humulene)
    Saturated fatty acids (e.g. isovaleric acid (3-methylbutanoic acid), myristic acid, palmitic acid, stearic acid)
    Alkanols (e.g. 1-tetracosanol, 1-hexacosanol)
    Vitamins & their analogues (e.g. carotenoids, choline, nicotinamide, nicotinic acid)
    Miscellaneous others (e.g. pectin, β-sitosterol, hexadecane, triacontane, kielcorin, norathyriol)

The naphthodianthrones hypericin and pseudohypericin along with the phloroglucinol derivative hyperforin are thought to be among the numerous active constituents.[2][107][108][109] It also contains essential oils composed mainly of sesquiterpenes.[2]
Selected chemical constituents of Hypericum perforatum

[show]
Research

St John's wort is being studied for effectiveness in the treatment of certain somatoform disorders. Results from the initial studies are mixed and still inconclusive; some research has found no effectiveness, other research has found a slight lightening of symptoms. Further study is needed and is being performed.

A major constituent chemical, hyperforin, may be useful for treatment of alcoholism, although dosage, safety and efficacy have not been studied.[110][111] Hyperforin has also displayed antibacterial properties against Gram-positive bacteria, although dosage, safety and efficacy has not been studied.[112] Herbal medicine has also employed lipophilic extracts from St John's wort as a topical remedy for wounds, abrasions, burns, and muscle pain.[111] The positive effects that have been observed are generally attributed to hyperforin due to its possible antibacterial and anti-inflammatory effects.[111] For this reason hyperforin may be useful in the treatment of infected wounds and inflammatory skin diseases.[111] In response to hyperforin's incorporation into a new bath oil, a study to assess potential skin irritation was conducted which found good skin tolerance of St John's wort.[111]

Hypericin and pseudohypericin have shown both antiviral and antibacterial activities. It is believed that these molecules bind non-specifically to viral and cellular membranes and can result in photo-oxidation of the pathogens to kill them.[2]

Concentrations of bioactive substances can be altered by regulating the environment during plant growth like different levels of UV-B radiation, for instance.[113]

Multiple studies have examined whether St John's wort improves some aspects of cognitive performance. Most studies have focused on the effect in rodents. A recent meta-analysis of 13 animal studies shows that administration of St John's wort improved performance in maze tasks in rodents (assessing long term or working memory).[114] This meta-analysis also demonstrated that the cognitive enhancing effect, while stronger for rodents who had been subjected to stress impairments, was also considerable in healthy rodents. No study in humans has yet demonstrated such nootropic effects.
See also

    Dietary supplement
    EU Food supplements directive
    List of plants poisonous to equines

Notes

    Less common names and synonyms include Tipton's weed, rosin rose, goatweed, chase-devil, or Klamath weed.[2]

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1. Arachidonate 5-lipoxygenase ...Specific function: Catalyzes the first step in leukotriene biosynthesis, and thereby plays a role in inflammatory processes ...
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    Ben Eliezer D, Yechiam E (2016). "Hypericum perforatum as a cognitive enhancer in rodents: A meta-analysis". Scientific Reports. 6 (36700). doi:10.1038/srep35700.

Further reading

    British Herbal Medicine Association Scientific Committee (1983). British Herbal Pharmacopoeia. West Yorkshire: British Herbal Medicine Association. ISBN 0-903032-07-4.
    Müller, Walter (2005). St. John's Wort and its Active Principles in Depression and Anxiety. Basel: Birkhäuser. ISBN 978-3-7643-6160-0. doi:10.1007/b137619.

Yucca Root

This is whole root or portions of Yucca neomexicana, the New Mexican Spanish bayonet, dug fresh by me in South West New Mexico.  When I use this I just let some small pieces of root soak in wate for a few hours, then drink the water.  It is not too tasty, but it works.  It is a good anti-inflammatory, and safe for pets.  It is especially useful for cats, who are always testing their limits and trying to be super cat.  When dosing pets, pieces of the root can sometimes be put in the water bowl. At this time I am not growing this myself.   The wikipedia article is below:

Yucca
From Wikipedia, the free encyclopedia
This article is about the genus comprising species of perennials, shrubs, and trees. For yuca, the term in many Latin American dialects for a species of root vegetable, see Cassava. For other uses, see Yucca (disambiguation).
Yucca
Yucca filamentosa.jpg
Yucca filamentosa naturalized in New Zealand
Scientific classification e
Kingdom:     Plantae
Clade:     Angiosperms
Clade:     Monocots
Order:     Asparagales
Family:     Asparagaceae
Subfamily:     Agavoideae
Genus:     Yucca
L.
Species

See text.
Synonyms

Clistoyucca (Engelm.) Trel.
Samuela Trel.
Sarcoyucca (Engelm.) Linding.[1]

Yucca is a genus of perennial shrubs and trees in the family Asparagaceae, subfamily Agavoideae.[2] Its 40-50 species are notable for their rosettes of evergreen, tough, sword-shaped leaves and large terminal panicles of white or whitish flowers. They are native to the hot and dry (arid) parts of the Americas and the Caribbean. Early reports of the species were confused with the cassava (Manihot esculenta).[3] Consequently, Linnaeus mistakenly derived the generic name from the Taíno word for the latter, yuca (spelled with a single "c").[4] It is commonly found growing in rural graveyards and when in bloom the cluster of (usually pale) flowers on a thin stalk appear as floating apparitions.[5]

Contents

    1 Distribution
    2 Ecology
    3 Adaptations
    4 Uses
        4.1 Gastronomy
    5 Cultivation
    6 Symbolism
    7 Species
    8 Taxonomic arrangement
    9 Cultivars
    10 Gallery
    11 References
    12 External links

Distribution
Distribution of the capsular fruited species in southwest, midwest USA, Mexico's Baja California and Canada, overview

The natural distribution range of the genus Yucca (49 species and 24 subspecies) covers a vast area of the Americas. The genus is represented throughout Mexico and extends into Guatemala (Yucca guatemalensis). It also extends to the north through Baja California in the west, northwards into the southwestern United States, through the drier central states as far north as southern Alberta in Canada (Yucca glauca ssp. albertana). Yucca is also native to the lowlands and dry beach scrub of the Gulf and South Atlantic States from coastal Texas to easternmost Virginia. Yuccas have adapted to an equally vast range of climatic and ecological conditions. They are to be found in rocky deserts and badlands, in prairies and grassland, in mountainous regions, in light woodland, in coastal sands (Yucca filamentosa), and even in subtropical and semitemperate zones, although these are generally arid to semi-arid.
Ecology

Yuccas have a very specialized, mutualistic pollination system, being pollinated by yucca moths (family Prodoxidae); the insect purposefully transfers the pollen from the stamens of one plant to the stigma of another, and at the same time lays an egg in the flower; the moth larva then feeds on some of the developing seeds, always leaving enough seed to perpetuate the species. Certain species of the yucca moth have evolved antagonistic features against the plant and do not assist in the plants pollination efforts while continuing to lay their eggs in the plant for protection.[6] Yucca species are the host plants for the caterpillars of the yucca giant-skipper (Megathymus yuccae),[7] ursine giant-skipper (Megathymus ursus),[8] and Strecker's giant-skipper (Megathymus streckeri).[9]
Large Joshua tree with thick trunk at Grapevine Springs Ranch, AZ
Purplish fruits of Yucca aloifolia.
Adaptations
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Species of yucca have adapted to a wide variety of climates in mountains, coastal sand, grasslands and prairies as well as rocky badlands and deserts. Most species of yucca have thick, waxy skins to prevent loss of water through evaporation. They frequently store water in thick roots. Some yuccas store water in thick, fleshy leaves. Some desert plants have an oily coating on their leaves or pads that traps moisture, thereby reducing water loss. Some species drop their leaves during drought to prevent the loss of water through transpiration. Dead leaves of yucca collecting against the trunk of the trees help protect it from the sun. The channeled leaves of a yucca direct dew and rainfall water to their roots. Yuccas are said to be "fire adapted"; that is, they grow and spread vigorously after wildfires.
Uses

Yuccas are widely grown as ornamental plants in gardens. Many species also bear edible parts, including fruits, seeds, flowers, flowering stems,[10] and more rarely roots. References to yucca root as food often arise from confusion with the similarly pronounced, but botanically unrelated, yuca, also called cassava or manioc (Manihot esculenta). Roots of soaptree yucca (Yucca elata) are high in saponins and are used as a shampoo in Native American rituals. Dried yucca leaves and trunk fibers have a low ignition temperature, making the plant desirable for use in starting fires via friction.[11] In rural Appalachian areas, species such as Yucca filamentosa are referred to as "meat hangers". The tough, fibrous leaves with their sharp-spined tips were used to puncture meat and knotted to form a loop with which to hang meat for salt curing or in smoke houses.
Gastronomy

The flower petals are eaten. The petals are blanched for just 5 minutes, and then cooked a la mexicana (with tomato, onion, chile) or in tortitas con salsa (egg-battered patties with green or red sauce). Reproductive organs are removed before blanching because they are too bitter.
Cultivation

Yuccas are widely grown as architectural plants providing a dramatic accent to landscape design. They tolerate a range of conditions, but are best grown in full sun in subtropical or mild temperate areas. In gardening centres and horticultural catalogues they are usually grouped with other architectural plants such as cordylines and phormiums.[12]

Joshua trees (Yucca brevifolia) are protected by law in some states. A permit is needed for wild collection. As a landscape plant, they can be killed by excessive water during their summer dormant phase, so are avoided by landscape contractors.

Several species of yucca can be grown outdoors in temperate climates, these include:-[12]

    Y. filamentosa   
    Y. flaccida

  

    Y. gloriosa
    Y. recurvifolia

Symbolism

The "yucca flower" is the state flower of New Mexico. No species name is given in the citation.
Species

As of February 2012, the World Checklist of Selected Plant Families recognizes 49 species of Yucca and a number of hybrids:[13]
        Species name     Common name
Yucca aloifolia 4.jpg     Yucca-aloifolia-20071002-2.jpg     Yucca aloifolia L. (Type species) (syn. Yucca yucatana)     Aloe yucca, Spanish bayonet
Yucca angustissima fh 1179.14 AZ B.jpg         Yucca angustissima Engelm. ex Trel. (including Yucca kanabensis)     Narrowleaf yucca, Spanish bayonet
Yucca arkansana fh 1185.30 TX B.jpg         Yucca arkansana Trel.   
Yucca baccata whole.jpg     Yucca baccata close.jpg     Yucca baccata Torr. (including Yucca thornberi)     Banana yucca, datil
Yucca baileyi.jpg         Yucca baileyi Wooton & Standl. (syn. Yucca standleyi McKelvey)   
Joshua Tree in Joshua Tree National Park.jpg     Yucca brevifolia flower.jpg     Yucca brevifolia Engelm.     Joshua tree
Yucca campestris fh 1179.82 BB.jpg         Yucca campestris McKelvey   
Yucca capensis fh 0619 Baja California Sur B.jpg         Yucca capensis L.W.Lenz   
Yucca carnerosana fh 1179.26 TX B.jpg         Yucca carnerosana (Trel.) McKelvey   
Yucca cernua fh 1185.31 TX BB.JPG         Yucca cernua E.L.Keith   
Yucca coahuilensis fh 1184.45 TX BB.jpg         Yucca coahuilensis Matuda & I.L.Pina   
Yucca constricta fh 1180.67 TX B.jpg         Yucca constricta Buckley     Buckley's yucca
Yucca decipiens.jpg     Yucca decipiens 2.jpg     Yucca decipiens Trel.     Palma China
        Yucca declinata Laferr.   
        Yucca desmetiana Baker   
Yucca elata blooming.jpg     Yucca elata flowers.jpg     Yucca elata (Engelm.) Engelm.     Soaptree yucca
Yucca endlichiana fh 0334 MEX B.jpg         Yucca endlichiana Trel.   
Yucca torreyi fh 1180.18 TX B.jpg         Yucca faxoniana Sarg. (syn. Yucca torreyi)     Torrey yucca
Yucca filamentosa.jpg     Yucca filamentosa1.jpg     Yucca filamentosa L.     Spoonleaf yucca, Filament yucca, or Adam's Needle
Yucca filifera Monaco.jpg         Yucca filifera Chabaud     Palma Chuna yucca
Yucca flaccida.jpg         Yucca flaccida Haw.     Flaccid leaf yucca
Barcelona 354.JPG         Yucca gigantea Lem. (syn. Yucca guatemalensis)     Spineless yucca
Yucca glauca soapweed MN 2007.JPG     Yucca glauca Sinijukka VII08 H6193.jpg     Yucca glauca Nutt.     Great Plains yucca
Yucca gloriosa 10.JPG         Yucca gloriosa L. (including Yucca recurvifolia)     Moundlily yucca, Adam's needle, Spanish dagger
Yucca grandiflora fh 0401 MEX B.jpg         Yucca grandiflora Gentry     Sahuiliqui yucca
Yucca harrimaniae fh 1179.13 UT B.jpg         Yucca harrimaniae Trel. (syn. Yucca nana)     Harriman's yucca
Yucca baileyi subsp. intermedia fh 1179.25 NM B.jpg         Yucca intermedia McKelvey     Intermediate yucca
Yucca jaliscensis.jpg         Yucca jaliscensis (Trel.) Trel.     Izote
Yucca lacandonica fh 0376 MEX B.jpg         Yucca lacandonica Gómez Pompa & J.Valdés     Tropical yucca
Yucca linearifolia MEX BB.jpg         Yucca linearifolia Clary   
Mexican Blue Yucca, Rio Grande Botanic Garden, Albuquerque NM.jpg         Yucca luminosa (syn. Yucca rigida)     Blue yucca
        Yucca madrensis Gentry     Soco yucca
Yucca mixtecana fh 0380 MEX B.jpg         Yucca mixtecana García-Mend.   
        Yucca necopina Shinners   
Yucca harrimaniae subsp. neomexicana fh 1180.76 COL B.jpg         Yucca neomexicana Wooton & Standl.     New Mexican Spanish bayonet
Yucca pallida.jpg         Yucca pallida McKelvey     Pale yucca
Yucca periculosa 1.jpg         Yucca periculosa Baker     Izote
Yucca potosina fh 0388 MEX B.jpg         Yucca potosina Rzed.   
Yucca queretaroensis fh 0335 MEX B.jpg         Yucca queretaroensis Piña Luján   
Yucca reverchonii - Botanischer Garten der Universität Würzburg.JPG         Yucca reverchonii Trel.   
Yucca rostrata.jpg         Yucca rostrata Engelm. ex Trel.     Beaked yucca, Big Bend yucca
Yucca rupicola.jpg         Yucca rupicola Scheele     Texas yucca, or twist-leaf yucca
Yucca schidigera blooming.jpg         Yucca schidigera Roezl ex Ortgies     Mojave yucca
Monaco.Jardin exotique014.jpg         Yucca × schottii     Hoary yucca or mountain yucca
Yucca harrimanniae subsp. sterilis fh 1179. 78 UT B.jpg         Yucca sterilis (Neese & S.L.Welsh) S.L.Welsh & L.C.Higgins   
        Yucca tenuistyla Trel.   
Yucca brooklyn.jpg         Yucca thompsoniana Trel.     Thompson's yucca
Yucca treculeana (as Yucca canaliculata) Bot. Mag. 86. t. 5201. 1860..jpg         Yucca treculeana Carrière     Texas bayonet, Trecul's yucca
Yucca utahensis 4.jpg     Yucca utahensis 1.jpg     Yucca utahensis McKelvey   
Yucca valida fh 0602 BC B.jpg         Yucca valida Brandegee     Datilillo

A number of other species previously classified in Yucca are now classified in the genera Dasylirion, Furcraea, Hesperaloe, Hesperoyucca, and Nolina.
Taxonomic arrangement
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    Section Yucca formerly Sarcocarpa Engelm.
        Series Faxonianae Hochstätter
            Yucca carnerosana (Trel.) McKelvey
            Yucca faxoniana (Trel.) Sarg.
        Series Baccatae Hochstätter
            Yucca baccata Torr.
                Yucca baccata Torr. ssp. baccata
                Yucca baccata Torr. ssp. vespertina (McKelvey) Hochstätter
                Yucca baccata Torr. ssp. thornberi (McKelvey) Hochstätter
            Yucca confinis McKelvey
            Yucca endlichiana Trel.
            Yucca arizonica McKelvey
        Series Treculianae Hochstätter
            Yucca grandiflora Gentry
            Yucca declinata Laferr.
            Yucca treculiana Carriere
            Yucca torreyi Shafer
            Yucca schidgera Roezl ex Ortgies
            Yucca schotti Engelm.
            Yucca capensis Lenz
            Yucca jaliscensis Trel.
            Yucca periculosa Baker
            Yucca mixtecana Garcia-Mend.
            Yucca decipiens Trel.
            Yucca valida Brandegee
            Yucca potosina Rzed.
            Yucca filifera Chabaud
        Series Gloriosae Hochstätter
            Yucca gloriosa L.
            Yucca recurvifolia Salisb.
        Series Yucca
            Yucca madrensis Gentry
            Yucca linearifolia Clary
            Yucca elephantipes Regel
            Yucca lacandonica Gomez-Pompa & Valdes
            Yucca aloifolia L.
            Yucca yucatana Engelm.
    Section Clistocarpa Engelm.
            Yucca brevifolia Engelm.)
                Yucca brevifolia Engelm. ssp. brevifolia
                Yucca brevifolia Engelm. ssp. jaegeriana (McKelvey) Hochstätter
                Yucca brevifolia Engelm. ssp. herbertii (Webber) Hochstätter
    Section Chaenocarpa Engelm.
        Series Filamentosae Hochstätter
            Yucca filamentosa L.
                Yucca filamentosa L. ssp. filamentosa
                Yucca filamentosa L. ssp. smalliana (Fernald) Hochstätter
                Yucca filamentosa L. ssp. concava (Haw.) Hochstätter
            Yucca flaccida Haw.
        Series Rupicolae Hochstätter
            Yucca cernua Keith
            Yucca pallida McKelvey
            Yucca queretaroensis Pina Lujan
            Yucca reverchonii Trel.
            Yucca rigida (Engelm.) Trel.
            Yucca rostrata Engelm. ex Trel.
            Yucca rupicola Scheele
            Yucca thompsoniana Trel.
        Series Harrimaniae Hochstätter
            Yucca harrimaniae Trel.
                Yucca harrimaniae Trel. ssp. harrimaniae
                Yucca harrimaniae Trel. ssp. neomexicana (Wooton & Standl.) Hochstätter
                Yucca harrimaniae Trel. ssp. sterilis (Neese & Welsh) Hochstätter
                Yucca harrimaniae Trel. ssp. gilbertiana (Trel.) Hochstätter
            Yucca nana Hochstätter
        Series Glaucae (McKelvey) Hochstätter
            Yucca angustissima Engelm. ex Trel.
                Yucca angustissima Engelm. ex Trel. ssp. angustissima
                Yucca angustissima Engelm. ex Trel. ssp. toftiae (Welsh) Hochstätter
                Yucca angustissima Engelm. ex Trel. ssp. kanabensis (McKelvey) Hochstätter
                Yucca angustissima Engelm. ex Trel. ssp. avia (Reveal) Hochstätter
            Yucca baileyi Wooton & Standl.
                Yucca baileyi Wooton & Standl. ssp. baileyi
                Yucca baileyi Wooton & Standl. ssp. intermedia (McKelvey) Hochstätter
            Yucca coahuilensis Matuda & Pinja Lujan
            Yucca elata Engelm.
                Yucca elata Engelm. ssp. elata
                Yucca elata Engelm. ssp. utahensis (McKelvey) Hochstätter
                Yucca elata Engelm. ssp. verdiensis (McKelvey) Hochstätter
            Yucca glauca Nutt.
                Yucca glauca Nutt. ssp. glauca
                Yucca glauca Nutt. ssp. stricta (Sims) Hochstätter
                Yucca glauca Nutt. ssp. albertana Hochstätter
            Yucca campestris McKelvey
            Yucca constricta Buckley
            Yucca arkansana Trel.
                Yucca arkansana Trel. ssp. arkansana
                Yucca arkansana Trel. ssp. louisianensis (Trel.) Hochstätter
                Yucca arkansana Trel. ssp. freemanni (Shinners) Hochstätter
    Section Hesperoyucca Engelm.
        (Treated as a separate genus Hesperoyucca by some sources.)
            Yucca whipplei Torr.
                Yucca whipplei Torr. ssp. whipplei
                Yucca whipplei Torr. ssp. caespitosa (Jones) Haines
                Yucca whipplei Torr. ssp. intermedia Haines
                Yucca whipplei Torr. ssp. percursa Haines
                Yucca whipplei Torr. ssp. newberryi (McKelvey) Hochstätter
                Yucca whipplei Torr. ssp. eremica Epling & Haines

Cultivars

In the years from 1897 to 1907, Carl Ludwig Sprenger created and named 122 Yucca hybrids.
Gallery

    Joshua trees (Yucca brevifolia), growing in the Mojave Desert

    Unknown species near Orosí, Costa Rica

    Yucca near Carlsbad Caverns National Park in New Mexico

    Yucca harrimaniae also known as Harriman's yucca

    Yucca faxoniana in Texas, with mature fruits

    Yucca schidigera in Nevada, in full bloom

References

"Yucca L.". Germplasm Resources Information Network. United States Department of Agriculture. 2010-01-19. Retrieved 2010-06-07.
Chase, M.W.; Reveal, J.L. & Fay, M.F. (2009), "A subfamilial classification for the expanded asparagalean families Amaryllidaceae, Asparagaceae and Xanthorrhoeaceae", Botanical Journal of the Linnean Society, 161 (2): 132–136, doi:10.1111/j.1095-8339.2009.00999.x
Irish, Gary (2000). Agaves, Yuccas, and Related Plants: a Gardener's Guide. Timber Press. p. 18. ISBN 978-0-88192-442-8.
Quattrocchi, Umberto (2000). CRC World Dictionary of Plant Names. 4 R-Z. Taylor & Francis US. p. 2862. ISBN 978-0-8493-2678-3.
Winslow, Chris (January 18, 2012). "Yuccas: 'Ghosts in the Graveyard'". Hays Free Press (Hays County, Texas) (Vol. 109, No. 41). Hays County, Texas: Barton Publications, Inc. p. 1C. Retrieved 5 February 2015. "Another more evocative name for them is 'ghosts in the graveyard.' This comes from the high number of yuccas growing wild in forgotten graveyards, where their large white flower clusters appear as 'ghosts' in the moonlight."
SEGRAVES, KARI A.; ALTHOFF, DAVID M.; PELLMYR, OLLE (1 October 2008). "The evolutionary ecology of cheating: does superficial oviposition facilitate the evolution of a cheater yucca moth?". Ecological Entomology. 33 (6): 765–770. doi:10.1111/j.1365-2311.2008.01031.x.
Daniels, Jaret C. "Yucca Giant-Skipper Butterfly, Megathymus yuccae (Boisduval & Leconte) (Insecta: Lepidoptera: Hesperiidae)". Electronic Data Information Source. University of Florida IFAS Extension. Retrieved 2010-06-07.
"Ursine Giant-Skipper Megathymus ursus Poling, 1902". Butterflies and Moths of North America. Retrieved 2010-06-07.
"Strecker's Giant-Skipper Megathymus streckeri (Skinner, 1895)". Butterflies and Moths of North America. Retrieved 2010-06-07.
Couplan, François (1998). The Encyclopedia of Edible Plants of North America. McGraw Hill Professional. ISBN 978-0-87983-821-8.
Baugh, Dick (1999). "the Miracle of Fire by Friction". In David Wescott. Primitive Technology: A Book of Earth Skills (10 ed.). pp. 32–33. ISBN 978-0-87905-911-8.
RHS A-Z encyclopedia of garden plants. United Kingdom: Dorling Kindersley. 2008. p. 1136. ISBN 1405332964.

    World Checklist of Selected Plant Families, The Board of Trustees of the Royal Botanic Gardens, Kew, retrieved 2012-02-23, search for "Yucca"

General

    Fritz Hochstätter (Hrsg.): Yucca (Agavaceae). Band 1 Dehiscent-fruited species in the Southwest and Midwest of the USA, Canada and Baja California , Selbst Verlag, 2000. ISBN 3-00-005946-6
    Fritz Hochstätter (Hrsg.): Yucca (Agavaceae). Band 2 Indehiscent-fruited species in the Southwest, Midwest and East of the USA, Selbst Verlag. 2002. ISBN 3-00-009008-8
    Fritz Hochstätter (Hrsg.): Yucca (Agavaceae). Band 3 Mexico , Selbst Verlag, 2004. ISBN 3-00-013124-8

External links
    Wikispecies has information related to: Yucca
    Look up Yucca in Wiktionary, the free dictionary.

    Yucca species and their Common names - Fritz Hochstätter
    New Mexico Statutes and Court Rules: State Flower