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抗 HIV 暴露前预防药物在结肠和阴道组织中的代谢差异。

Dissimilarities in the metabolism of antiretroviral drugs used in HIV pre-exposure prophylaxis in colon and vagina tissues.

机构信息

Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, 725N Wolfe St, WBSB 302, Baltimore, MD, 21205, USA.

出版信息

Biochem Pharmacol. 2013 Oct 1;86(7):979-90. doi: 10.1016/j.bcp.2013.08.013. Epub 2013 Aug 18.

Abstract

Attempts to prevent HIV infection through pre-exposure prophylaxis (PrEP) include topical application of anti-HIV drugs to the mucosal sites of infection; however, a potential role for local drug metabolizing enzymes in modulating the exposure of the mucosal tissues to these drugs has yet to be explored. Here we present the first report that enzymes belonging to the cytochrome P450 (CYP) and UDP-glucuronosyltransferase (UGT) families of drug metabolizing enzymes are expressed and active in vaginal and colorectal tissue using biopsies collected from healthy volunteers. In doing so, we discovered that dapivirine and maraviroc, a non-nucleoside reverse transcriptase inhibitor and an entry inhibitor currently in development as microbicides for HIV PrEP, are differentially metabolized in colorectal tissue and vaginal tissue. Taken together, these data should help to guide the optimization of small molecules being developed for HIV PrEP.

摘要

通过暴露前预防(PrEP)来预防 HIV 感染的尝试包括将抗 HIV 药物局部应用于感染的黏膜部位;然而,局部药物代谢酶在调节这些药物对黏膜组织的暴露方面的潜在作用尚未得到探索。在这里,我们首次报道了细胞色素 P450(CYP)和 UDP-葡糖醛酸基转移酶(UGT)家族的药物代谢酶在来自健康志愿者的活检组织中表达和活跃,存在于阴道和结直肠组织中。在这样做的过程中,我们发现,目前正在作为 HIV PrEP 的预防性杀微生物剂开发的非核苷类逆转录酶抑制剂和进入抑制剂地匹福林和马拉韦罗在结直肠组织和阴道组织中的代谢方式不同。总的来说,这些数据应该有助于指导正在开发的用于 HIV PrEP 的小分子的优化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2238/3807636/55300821037a/nihms516993f1.jpg

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