性情
药品
药理学
胃肠道
药物开发
生物
生物化学
心理学
社会心理学
作者
Song Gao,Rongjin Sun,Rashim Singh,Sik Yu So,Ching-Kit Chan,Tor Savidge,Ming Hu
标识
DOI:10.1016/j.drudis.2022.07.001
摘要
Gut microbial β-glucuronidase (gmGUS) is involved in the disposition of many endogenous and exogenous compounds. Preclinical studies have shown that inhibiting gmGUS activity affects drug disposition, resulting in reduced toxicity in the gastrointestinal tract (GIT) and enhanced systemic efficacy. Additionally, manipulating gmGUS activity is expected to be effective in preventing/treating local or systemic diseases. Although results from animal studies are promising, challenges remain in developing drugs by targeting gmGUS. Here, we review the role of gmGUS in host health under physiological and pathological conditions, the impact of gmGUS on the disposition of phenolic compounds, models used to study gmGUS activity, and the perspectives and challenges in developing drugs by targeting gmGUS.
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