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饮料-药物相互作用:饮用绿茶饮料对大鼠小肠和肝脏中阿托伐他汀代谢及膜转运蛋白的影响。

Beverage-Drug Interaction: Effects of Green Tea Beverage Consumption on Atorvastatin Metabolism and Membrane Transporters in the Small Intestine and Liver of Rats.

作者信息

Yao Hsien-Tsung, Hsu Ya-Ru, Li Mei-Ling

机构信息

Department of Nutrition, China Medical University, 91 Hsueh-shih Road, Taichung 404, Taiwan.

出版信息

Membranes (Basel). 2020 Sep 14;10(9):233. doi: 10.3390/membranes10090233.

Abstract

Green tea (GT) beverages are popular worldwide and may prevent the development of many chronic diseases including cardiovascular disease and cancer. To investigate whether the consumption of a GT beverage causes drug interactions, the effects of GT beverage consumption on atorvastatin metabolism and membrane transporters were evaluated. Male rats were fed a chow diet with tap water or the GT beverage for 3 weeks. Then, the rats were given a single oral dose (10 mg/kg body weight (BW)) of atorvastatin (ATV), and blood was collected at various time points within 6 h. The results show that GT consumption increased the plasma concentrations (AUC) of ATV (+85%) and 2-OH ATV (+93.3%). GT also increased the 2-OH ATV (+40.9%) and 4-OH ATV (+131.6%) contents in the liver. Decreased cytochrome P450 (CYP) 3A enzyme activity, with no change in P-glycoprotein expression in the intestine, was observed in rats treated with GT. Additionally, GT increased hepatic CYP3A-mediated ATV metabolism and decreased organic anion transporting polypeptides (OATP) 2 membrane protein expression. There was no significant difference in the membrane protein expression of OATP2B1 and P-glycoprotein in the intestine and liver after the GT treatment. The results show that GT consumption may lower hepatic OATP2 and, thus, limit hepatic drug uptake and increase plasma exposure to ATV and 2-OH ATV.

摘要

绿茶饮品在全球都很受欢迎,并且可能预防包括心血管疾病和癌症在内的多种慢性疾病的发生。为了研究饮用绿茶饮品是否会导致药物相互作用,评估了饮用绿茶饮品对阿托伐他汀代谢和膜转运蛋白的影响。雄性大鼠用自来水或绿茶饮品喂养3周。然后,给大鼠单次口服一剂(10毫克/千克体重)阿托伐他汀(ATV),并在6小时内的不同时间点采集血液。结果表明,饮用绿茶会增加ATV的血浆浓度(AUC)(增加85%)和2-羟基阿托伐他汀(2-OH ATV)的血浆浓度(增加93.3%)。绿茶还会增加肝脏中2-羟基阿托伐他汀(增加40.9%)和4-羟基阿托伐他汀(增加131.6%)的含量。在饮用绿茶的大鼠中观察到细胞色素P450(CYP)3A酶活性降低,而肠道中P-糖蛋白的表达没有变化。此外,绿茶会增加肝脏中CYP3A介导的阿托伐他汀代谢,并降低有机阴离子转运多肽(OATP)2膜蛋白的表达。饮用绿茶后,肠道和肝脏中OATP2B1和P-糖蛋白的膜蛋白表达没有显著差异。结果表明,饮用绿茶可能会降低肝脏中的OATP2,从而限制肝脏对药物的摄取,并增加血浆中阿托伐他汀和2-羟基阿托伐他汀的暴露量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3be4/7559440/c5ef4a6bb15e/membranes-10-00233-g001.jpg

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