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The liver toxicity biomarker study phase I: markers for the effects of tolcapone or entacapone.
Author: BalasubramanianRaji, BegerRichard D, BelandFrederick A, BoothShelagh A, CampbellJennifer M, ChangChing-Wei, ChenJames J, CourchesnePaul L, FanXiao-hui, FuscoeJames C, GraberArmin, GuoYu, HanTao, HinesWade M, JuhaszPeter, LiTricia Y, LynchMoira D, McBurneyRobert N, MolandCarrie L, MorelNicole M, PlastererThomas N, SchnackenbergLaura K, SuZhenqiang, TakachEdward J, TongWeida, VonTungelnLinda S, ZengChenhui
Original Abstract of the Article :
The Liver Toxicity Biomarker Study is a systems toxicology approach to discover biomarkers that are indicative of a drug's potential to cause human idiosyncratic drug-induced liver injury. In phase I, the molecular effects in rat liver and blood plasma induced by tolcapone (a "toxic" drug) were comp...See full text at original site
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引用元:
https://doi.org/10.1177/0192623312444026
データ提供:米国国立医学図書館(NLM)
Liver Toxicity Biomarker Study Phase I: Tolcapone vs. Entacapone
The field of toxicology is a complex and ever-evolving landscape, with researchers constantly seeking to understand the potential risks associated with drug use. This study investigates the molecular effects of two drugs, tolcapone and entacapone, on the liver. The researchers employed a systems toxicology approach to identify biomarkers, or molecular indicators, that could signal potential liver toxicity. The study involved comparing the molecular effects of tolcapone, a drug known to have a potential for liver toxicity, to those of entacapone, a drug considered relatively safe. Both drugs have similar chemical structures and primary mechanisms of action. The researchers examined the effects of both drugs on rat liver and blood plasma after 3 and 28 days of exposure.
Distinct Molecular Profiles
The study found that the marker analytes associated with tolcapone only partially overlapped with those associated with entacapone, despite their structural similarities. This suggests that the molecular analyses employed in the study are detecting substantial 'off-target' markers for both drugs. The researchers also observed a modest overlap in the marker data sets for the 3-day and 28-day exposures, indicating that the molecular changes in the liver and plasma caused by short-term and long-term drug treatments do not share common characteristics. These findings highlight the complexity of drug-induced liver injury and emphasize the importance of comprehensive molecular analyses to assess potential toxicity.
Understanding Drug Safety
This study highlights the importance of carefully evaluating the safety of new drugs, particularly those that may have potential for liver toxicity. The findings emphasize the need for comprehensive molecular analyses to identify potential biomarkers for drug-induced liver injury, which could help in the early detection and prevention of adverse effects.
Dr. Camel's Conclusion
This study is a reminder that even similar drugs can have different effects on the body. Just as different types of sand can create a diverse landscape, different drugs can trigger unique molecular responses. This research underscores the importance of careful monitoring and comprehensive evaluation in understanding drug safety and reducing the risk of adverse effects.
Date :
- Date Completed 2013-03-26
- Date Revised 2018-12-01
Further Info :
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