Ginseng
Ginseng as it relates to DILI in Health report: Genetics of Antibiotics-Induced Liver Injury
Ginseng and DILI
While ginseng is generally considered safe for most people when taken in appropriate doses, there have been reports of liver damage associated with the use of ginseng supplements. The exact mechanism by which ginseng may cause liver injury is not well understood, but it is believed to be related to the presence of certain compounds in ginseng that can be toxic to the liver.
It is important to note that the risk of liver injury from ginseng appears to be rare, and most people can safely consume ginseng without experiencing any adverse effects. However, individuals with pre-existing liver conditions or those taking medications that are metabolized by the liver should exercise caution when using ginseng supplements.
Conclusion
In conclusion, while ginseng is generally considered safe for most people, there have been rare cases of liver injury associated with its use. If you are considering taking ginseng supplements, it is advisable to consult with a healthcare provider to determine if it is safe for you, especially if you have a history of liver problems or are taking medications that may interact with ginseng.
Supplements for DILI
Here are some dietary supplements related to the content in this report. Click the shopping cart to purchase the supplement from our partners.
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Green tea extract
Contains catechins which may increase oxidative stress and liver cell damage when combined with hepatotoxic antibiotics.
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Greater celandine
Alkaloids like chelidonine may further impair liver function when the organ is under stress from antibiotics.
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Chaparral
Nordamnacanthal is a quinone that could synergistically increase antibiotic liver toxicity through mitochondrial dysfunction.
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Germander
Diterpenoids may amplify antibiotic liver injury by disrupting bile salt export and causing cholestasis.
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Mistletoe
Contains toxic lectins which could worsen immunological reactions or alter detox pathways of antibiotic metabolites.
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Skullcap
Flavonoids may inhibit pathways involved in hepatic metabolism and clearance of antibiotics from the liver.
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Valerian
Isovaltrate and other constituents thought to directly damage cell membranes, potentially worsening antibiotic hepatocellular toxicity.
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Kava kava
Kavalactones like desmethoxyyangonin may inhibit CYP450 liver enzymes important for antibiotic clearance.
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St. John's wort
Hyperforin alters PXR nuclear receptors and could decrease bile acid transport, contributing to antibiotic cholestasis.
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Ginseng
Ginsenosides may inhibit P-glycoprotein transporters important for antibiotic efflux from hepatocytes, allowing accumulation of toxic levels.
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Aloe vera
Anthraquinone glycosides possibly damage cell membranes and worsen antibiotic-mediated liver cell necrosis.
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Ashwagandha
Withanolides thought to cause oxidative stress which synergizes with redox-cycling antibiotic metabolites.
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Andrographis
Diterpene lactones may reduce bile acid secretion and flow, contributing to cholestatic injury.
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Noni juice
Anthraquinones could impair mitochondrial function and increase antibiotic hepatotoxicity.
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Peppermint oil
Menthol interferes with CYP450s and UGTs involved in antibiotic metabolism and clearance.
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Kratom
Mitragynine and 7-hydroxymitragynine are metabolized in liver and could enhance antibiotic toxicity.
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Ephedra
Ephedrine alkaloids may deplete glutathione and reduce the liver's defense against antibiotic oxidative damage.
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