亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

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 and 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
2秒前
Dore完成签到,获得积分10
3秒前
6秒前
顾矜应助feiying采纳,获得10
1分钟前
简单谷波发布了新的文献求助20
1分钟前
科研通AI2S应助科研通管家采纳,获得10
1分钟前
2分钟前
2分钟前
2分钟前
潜行者完成签到 ,获得积分10
2分钟前
3分钟前
feiying发布了新的文献求助10
3分钟前
Augustines发布了新的文献求助10
3分钟前
feiying完成签到,获得积分10
3分钟前
番茄酱狠好吃完成签到 ,获得积分10
3分钟前
3分钟前
9527发布了新的文献求助10
3分钟前
Orange应助科研通管家采纳,获得30
5分钟前
慕青应助科研通管家采纳,获得10
5分钟前
研友_ndDGVn完成签到,获得积分10
5分钟前
研友_ndDGVn发布了新的文献求助10
5分钟前
6分钟前
6分钟前
minnie完成签到 ,获得积分10
6分钟前
汉堡包应助肥猫采纳,获得10
7分钟前
科研通AI2S应助科研通管家采纳,获得10
7分钟前
7分钟前
8分钟前
肥猫发布了新的文献求助10
8分钟前
androabo完成签到,获得积分10
9分钟前
机智代亦完成签到,获得积分10
10分钟前
机智代亦发布了新的文献求助10
10分钟前
美满尔蓝完成签到,获得积分10
11分钟前
11分钟前
A29964095完成签到 ,获得积分10
11分钟前
12分钟前
lihongchi发布了新的文献求助10
12分钟前
lihongchi完成签到,获得积分10
12分钟前
4466完成签到,获得积分10
13分钟前
13分钟前
高分求助中
Overcoming Stigma and Bias in Obesity Management 800
Malcolm Fraser : a biography 700
Signals, Systems, and Signal Processing 610
Bounds for Statistical Estimation in Semiparametric Models 500
Climate change and sports: Statistics report on climate change and sports 500
Forced degradation and stability indicating LC method for Letrozole: A stress testing guide 500
Ideology and Meaning-Making under the Putin Regime 450
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6472931
求助须知:如何正确求助?哪些是违规求助? 8276421
关于积分的说明 17646603
捐赠科研通 5552527
什么是DOI,文献DOI怎么找? 2909655
邀请新用户注册赠送积分活动 1886432
关于科研通互助平台的介绍 1738029