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Last Updated: 3 years ago

Possible Interaction: Ethanol and Allyl Sulfide

supplement:

Ethanol

supplement:

Allyl Sulfide

Research Papers that Mention the Interaction

Further, we showed that DAS reduced the expression of lipogenic genes and improved lipid accumulation and adipocyte mass in human primary adipocytes treated with EtOH.
Subsequently, we also showed that oxidative stress, as measured by the changes in MDA levels, was reduced in both male Wistar rats and human primary adipocytes treated with EtOH plus DAS.
Alcoholism, clinical and experimental research  •  2017  |  View Paper
DAS is a selective inhibitor of cytochrome P450 2E1 (CYP2E1), which is known to metabolize many xenobiotics including alcohol and analgesic drugs in the liver.
Several groups have shown that DAS is not only capable of inhibiting alcohol- and drug-mediated cellular toxicities, but also HIV protein- and diabetes-mediated toxicities by selectively inhibiting CYP2E1 in various cell types.
Current drug metabolism  •  2015  |  View Paper
Ethanol led to elevated levels of CYP2E1, iNOS and phospholamban, decreased levels of HO-1 and Na(+)Ca(2+) exchanger, cardiac contractile and intracellular …, overt O(2)(-) production, and apoptosis accompanied with increased phosphorylation of JNK and ASK-1, the effects were significantly attenuated or ablated by diallyl sulfide.
Biochimica et biophysica acta  •  2013  |  View Paper
Diallyl sulfide DAS ) has been shown to prevent xenobiotic (e.g. ethanol , acetaminophen) induced toxicity and disease (e.g. HIV-1) pathogenesis.
Toxicology letters  •  2018  |  View Paper
Diallyl sulfide DAS ), a selective inhibitor of CYP2E1, has shown protective effects against alcohol‐ and acetaminophen‐induced hepatotoxicity in many studies.
Pharmacology research & perspectives  •  2017  |  View Paper
Ethanol toxicity was prevented by 4-methylpyrazole and by diallyl sulfide , inhibitors of CYP2E1.
The Journal of Biological Chemistry  •  1996  |  View Paper
Further, 100 μM DAS also improved the levels of lipid accumulation in 3T3L1 adipocytes that was down-regulated by ethanol exposure.
Further, treatment of ethanol-exposed 3T3L1 cells with 100 μM DAS for 24 h was found to reduce ethanol induced ROS production, expression of pro-inflammatory cytokines, and enhance anti-inflammatory cytokine production in the cells.
Taken together, our study results imply that DAS may be effective in reducing ethanol induced injury of cells thereby suggesting its potential to be used in drug formulations.
Drug and chemical toxicology  •  2018  |  View Paper
Ethanol and DAS additively induced hepatic hyperplasia (P<.05).
Alcohol  •  2010  |  View Paper
A time- and dose-dependent induction in COL1A2 mRNA by ethanol or AA was observed that was prevented by diallylsulfide , a CYP2E1 inhibitor.
The Journal of Biological Chemistry  •  2000  |  View Paper
These parameters in neurons were relatively unaffected when the cells were incubated with … of inhibitors of alcohol-oxidizing enzymes, but in thymocytes, the presence of diallyl sulfide (an inhibitor of alcohol-inducible cytochrome P450, CYP2E1) or 4-methylpyrazole (… CYP2E1 and alcohol dehydrogenase) caused decreases in ROS production from ethanol.
Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology  •  1999  |  View Paper
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