Organic Anion–Transporting Polypeptide (OATP)–Mediated Drug-Drug Interaction Study between Rosuvastatin and Cyclosporine A in Chimeric Mice with Humanized Liver

瑞舒伐他汀 药理学 药代动力学 药品 有机阴离子转运多肽 药物代谢 运输机 药物与药物的相互作用 药物相互作用 细胞色素P450 化学 医学 生物化学 基因
作者
Masashi Uchida,Yoriko Tajima,Masakazu Kakuni,Yutaka Kageyama,Taro Okada,Eri Sakurada,Chise Tateno,Ryoji Hayashi
出处
期刊:Drug Metabolism and Disposition [American Society for Pharmacology & Experimental Therapeutics]
卷期号:46 (1): 11-19 被引量:31
标识
DOI:10.1124/dmd.117.075994
摘要

The influence of transporters on the pharmacokinetics of drugs is being increasingly recognized, and DDIs via transporters may be a risk factor for adverse events. Cyclosporine A, a strong OATP inhibitor, has been reported to increase the systemic exposure of rosuvastatin, an OATP substrate, by 7.1-fold in clinical studies. PXB mice are chimeric mice with humanized livers that are highly repopulated with human hepatocytes and have been widely used for drug discovery in drug metabolism and pharmacokinetics studies. In the present study, we examined in vivo and in vitro DDIs between rosuvastatin and cyclosporine A in PXB mice and fresh human hepatocytes (PXB cells) obtained from PXB mice. We initially investigated the active transport of rosuvastatin into PXB cells, and found concentration-dependent uptake with a Michaelis-Menten constant value of 4.0 μmol/l and a Vmax value of 4.63 pmol/min per 106 cells. Cyclosporine A inhibited the uptake of rosuvastatin with an IC50 value of 0.21 μmol/l. We then examined in vivo DDIs, and the exposure of orally administered rosuvastatin increased by 3.3-fold and 11-fold in PXB mice pretreated with 10 and 50 mg/kg cyclosporine A, whereas it increased by 2.5-fold and 6.2-fold when rosuvastatin was administered intravenously, in studies that were conducted for considering gastrointestinal DDIs. The liver-to-blood concentration ratio of rosuvastatin was dose-dependently decreased by pretreatment with cyclosporine A in PXB mice and SCID mice. Observed DDIs in vivo were considered to be reasonable based on the estimated concentrations of cyclosporine A at the inlet to the liver and in the liver tissues of both mice. In conclusion, our results indicate that PXB mice might be a useful tool for predicting human OATP-mediated DDIs in drug discovery, and its limitation due to the differences of gastrointestinal condition from human should also be considered.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
黑怕完成签到,获得积分10
刚刚
小手冰凉完成签到 ,获得积分10
1秒前
ZYW完成签到,获得积分10
2秒前
CodeCraft应助wc采纳,获得10
2秒前
瓜农完成签到,获得积分10
2秒前
重要的板凳完成签到,获得积分10
2秒前
幸运雨点完成签到,获得积分10
4秒前
飞翔的鸣完成签到,获得积分0
5秒前
杨茗涵完成签到,获得积分10
5秒前
chen完成签到 ,获得积分10
5秒前
生命科学完成签到 ,获得积分10
5秒前
66完成签到,获得积分10
7秒前
JYCKLTY完成签到,获得积分10
8秒前
谦让的冷珍完成签到,获得积分10
8秒前
机智笑南完成签到,获得积分10
9秒前
逢投必中完成签到 ,获得积分10
9秒前
JXDYYZK完成签到,获得积分10
9秒前
xiao完成签到 ,获得积分10
11秒前
孤独丹秋完成签到,获得积分10
11秒前
Swu完成签到,获得积分10
14秒前
hhhhhjn完成签到,获得积分10
14秒前
ysw完成签到,获得积分10
14秒前
阳光完成签到,获得积分10
15秒前
miemie66完成签到,获得积分10
15秒前
奉雨眠完成签到,获得积分10
15秒前
含蓄文博完成签到 ,获得积分0
17秒前
xiao6fan完成签到 ,获得积分10
17秒前
慕青应助wc采纳,获得10
18秒前
CDI和LIB完成签到,获得积分10
18秒前
Ray完成签到,获得积分0
18秒前
贤弟完成签到,获得积分10
20秒前
Star完成签到,获得积分0
21秒前
专注的雪完成签到 ,获得积分10
22秒前
22秒前
枫威完成签到 ,获得积分10
22秒前
叶赛文完成签到,获得积分10
23秒前
鸡蛋酱完成签到 ,获得积分10
23秒前
Tynn完成签到 ,获得积分10
24秒前
研友Bn完成签到 ,获得积分10
24秒前
怕孤单的初蝶完成签到,获得积分10
25秒前
高分求助中
Modern Epidemiology, Fourth Edition 5000
Kinesiophobia : a new view of chronic pain behavior 5000
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 3000
Digital Twins of Advanced Materials Processing 2000
Propeller Design 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
First commercial application of ELCRES™ HTV150A film in Nichicon capacitors for AC-DC inverters: SABIC at PCIM Europe 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 化学工程 生物化学 物理 计算机科学 内科学 复合材料 催化作用 物理化学 光电子学 电极 冶金 细胞生物学 基因
热门帖子
关注 科研通微信公众号,转发送积分 6005067
求助须知:如何正确求助?哪些是违规求助? 7527288
关于积分的说明 16112532
捐赠科研通 5150611
什么是DOI,文献DOI怎么找? 2759803
邀请新用户注册赠送积分活动 1736889
关于科研通互助平台的介绍 1632141