Regulation of CYP450 and drug transporter mediated by gut microbiota under high-altitude hypoxia

被引:7
作者
Bai, Xue [1 ,2 ]
Yang, Jianxin [1 ]
Liu, Guiqin [1 ]
Zhu, Junbo [1 ]
Wang, Qian [3 ]
Gu, Wenqi [3 ]
La, Linli [3 ]
Li, Xiangyang [1 ,2 ]
机构
[1] Qinghai Univ, Res Ctr High Altitude Med, Med Coll, Xining, Peoples R China
[2] Qinghai Univ, State Key Lab Plateau Ecol & Agr, Xining, Peoples R China
[3] Qinghai Univ, Med Coll, Xining, Peoples R China
基金
中国国家自然科学基金;
关键词
cytochrome P450; drug metabolism; drug transporter; gut microbiota; high-altitude hypoxia; DOWN-REGULATION; PREVENTION; EXPRESSION; PHARMACOKINETICS; CYTOCHROME-P450; METABOLISM; CYP3A;
D O I
10.3389/fphar.2022.977370
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hypoxia, an essential feature of high-altitude environments, has a significant effect on drug metabolism. The hypoxia-gut microbiota-CYP450/drug transporter axis is emerging as a vital factor in drug metabolism. However, the mechanisms through which the gut microbiota mediates the regulation of CYP450/drug transporters under high-altitude hypoxia have not been well defined. In this study, we investigated the mechanisms underlying gut microbial changes in response to hypoxia. We compared 16S ribosomal RNA gene sequences of the gut microbiota from plain and hypoxic rats. As a result, we observed an altered gut microbial diversity and composition in rats under hypoxia. Our findings show that dysregulated gut microbiota changes CYP3A1 and MDR1 expressions in high-altitude hypoxic environments. Thus, our study reveals a novel mechanism underlying the functioning of the hypoxia-gut microbiota-CYP450/drug transporter axis.
引用
收藏
页数:12
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