Thanks to the University of North Carolina School of Pharmacy for the use of this article!
Michelle Giesler and Kimberly Jones
General Description
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Other names: Marian thistle, St. Mary's thistle, Our Lady's thistle
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Family: Asteraceae
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Distribution: Native to the Mediterranean region of Europe, but naturalized
in California and the eastern US
Description of plant:
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tall herb with prickly leaves and a milky sap
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Small, hard fruits (achenes), a feathery tuft or pappus is removed
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Milk white veins in the leaves (originated in the milk of the Virgin Mary
which once fell upon the plant)
Parts used:
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ripe fruit (not seeds), root, leaves, hull
Chemical composition
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Silymarin- chemical mixture of antihepatotoxic principles; 1-4% conc. in
fruit
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Shown to consist of a large number of flavonolignans, including principally
silybin accompanied by isosilybin, dehydrosilybin, silydianin, silychristin,
etc.
History and folk use
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Formerly frequently cultivated in gardens
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The stalks may be eaten and are palatable and nutritious
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Young leaves may be eaten as a salad, and were sometimes baked in pies
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The heads were formerly boiled and eaten, treated like those of an Artichoke
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Thought to be a great breeder of milk and proper diet for nursing women
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Thought to have a healing property in those with snake bites
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If worn around the neck it would protect you from snake bites
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Fruit formerly thought to cure hydrophobia
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Applied externally, said to have been proven beneficial in cases of cancer
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The young, tender plant be boiled and eaten in the spring as a blood cleanser
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Fruits have been used for many years for a variety of conditions, especially
liver complaints. However, medicinal use of the plant, except as a simple
bitter, was practically discontinued early in the twentieth century.
Primary effects in the body
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Acts on cell membranes of liver cells to prevent the entry of toxic substances
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Stimulates protein synthesis, accelerating regeneration process & production
of liver cells
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Acts as an antioxidant, with far greater free radical damage control than
vitamin E
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It may offer some protection against toxic side effects from acetaminophen
Clinical applications
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Early treatment for chronic liver problems
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Rehabilitation from alcohol, solvent or IV recreational abuse
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Protects hepatocytes from heavy metal, chemical and alcohol injury
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Limits fatty degeneration and speeds up hepatitis recovery, slowing or reversing
cirrhosis
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Supportive treatment for inflammatory liver conditions and cirrhosis
Toxicity
Drug and disease interactions
Dosage
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Fruit (seeds): 2-3 capsules up to 3 x day
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Tincture: 1:5, 60% alcohol, ½ to 1 teaspoon up to 4 x day (equal parts
of root & seed with hull attached)
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Silymarin is very poorly soluble in water so is not effective as a tea (<
10% plant activity)
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Poor solubility and poor absorption from GI tract (20-50%) make active principles
best administered parenterally
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Oral use requires a concentrated product
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Capsules containing 200mg of a concentrated extract representing 140mg of
silymarin
Primary and Tertiary literature
Protection from Amanita phalloides intoxication Tox Appl Pharm 73
(1984)
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Severe poisoning with mortality rate of 30%
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Study in beagles
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50 gm/kg silibinin 5 and 24 hrs post-intoxication
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4 deaths in control group / 0 deaths with silibinin
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Reduction in elevations of GPT, GOT, AP and bilirubin with silibinin; less
decrease in PT
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Mechanism of Action?
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Modification or occupance of cell membrane receptor sites
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Decrease phospholipid metabolism
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Prevention of inhibition of RNA Polymerase and RNA synthesis by toxin
Increase of Glutathione Content in the Liver Planta Medica 55
(1989)
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200 mg/kg silymarin single dose
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Over 50% increase GSH in liver and intestine
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Selectivity
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accumulation principally in liver
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entero-hepatic recirculation
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An increase in GSH can increase conjugation/elimination of toxins and decrease
lipid peroxidation
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Mechanism of action?
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Increase in membrane permeability of amino acids involved in GSH synthesis
Stimulation of DNA synthesis in malignant cell lines? Biochem Pharm
35(1986)
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27 mg/kg silibinin prior to injection of radioactive thymidine
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Silibinin increases ribosomal RNA synthesis
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No influence on DNA synthesis in normal livers
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Large increase in DNA synthesis in hepatectomized rats / 23-35% increase
in thymidine incorporation
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No influence on DNA synthesis in fast growing hepatoma cell cultures
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Mechanism of action?
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Hepatectomized rats
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If the regulatory signal for replication initiation is given, increase in
rRNA and protein synthesis also accelerates DNA synthesis
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Hepatoma cells
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The rate of proliferation is already maximal and cannot be further intensified
Effect of silibinin on biliary lipid composition Journal of Hepatology
12(1991)
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The rats
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100mg/kg or 50mg/kg silymarin for 7 days
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measured biliary cholesterol, biliary phospholipid, total bile salt and bile
flow
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decrease in biliary cholesterol and phosolipid
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no change in bile flow and total bile salts
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The Humans
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400mg/day silymarin in cholecystectomized and gallstone patients for 1 month
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significant decrease in biliary cholesterol for both groups
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Mechanism of Action?
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Found a dose dependent decrease in HMG-CoA reductase in the liver with increasing
silymarin concentration
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A decrease in HMG-CoA reductase leads to a decrease in synthesis of cholesterol
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