Binding of dorzolamide and its metabolite, N-deethylated dorzolamide, to human erythrocytes in vitro.

多佐酰胺 化学 代谢物 生物化学 生物物理学 生物 神经科学 噻吗洛尔 青光眼
作者
T. Hasegawa,Kaori Hara,Shunsuke HATA
出处
期刊:Drug Metabolism and Disposition [American Society for Pharmacology and Experimental Therapeutics]
卷期号:22 (3): 377-382 被引量:23
标识
DOI:10.1016/s0090-9556(25)08386-2
摘要

Dorzolamide, previously known as MK-507, is a novel topical carbonic anhydrase (CA) inhibitor. The uptake and binding of dorzolamide and its N-deethylated metabolite to human erythrocytes were studied in vitro. Dorzolamide and N-deethylated dorzolamide were preferentially taken up by the erythrocytes, and the uptake of dorzolamide by erythrocytes was found to be much faster than that of N-deethylated dorzolamide. When 20 or 200 microM dorzolamide was incubated with human erythrocytes, 98% or 71% of the drug was taken up by the erythrocytes, respectively. Similarly, using 20 or 200 microM N-deethylated dorzolamide, 99.7% or 75% of the drug was taken up by the erythrocytes, respectively. These results indicate that human erythrocytes contain proteins that bind to dorzolamide and N-deethylated dorzolamide, and the binding of these proteins is saturable. The results of the in vitro binding study suggest that presence of at least three kinds of binding site for dorzolamide in human erythrocytes. One of the binding sites for dorzolamide was characterized by extremely high affinity (Kd = 0.0011 microM) and low capacity (Bmax = 16.1 microM), corresponding to CA-II. Another binding site was characterized by low affinity (Kd = 2.8 microM) and high capacity (Bmax = 117.1 microM), corresponding to CA-I. The third one was a nonspecific binding. The binding of N-deethylated dorzolamide to human CA-I and CA-II was competitively inhibited by dorzolamide, indicating that these compounds bind to the same binding site on CAs. In each other's presence, most of dorzolamide in erythrocytes binds to CA-II, whereas the N-deethylated metabolite mainly binds to CA-I.(ABSTRACT TRUNCATED AT 250 WORDS)

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
刚刚
充电宝应助现代的绿真采纳,获得10
刚刚
幽默的老师完成签到,获得积分10
1秒前
ely发布了新的文献求助10
1秒前
lishuang完成签到,获得积分10
1秒前
UU完成签到,获得积分10
1秒前
Kevin完成签到,获得积分10
1秒前
sylvia发布了新的文献求助10
1秒前
1秒前
xixixiu72发布了新的文献求助10
1秒前
2秒前
3秒前
爱学习的向日葵完成签到,获得积分10
3秒前
szf完成签到,获得积分10
3秒前
3秒前
hys发布了新的文献求助10
4秒前
NexusExplorer应助无fh45采纳,获得10
4秒前
4秒前
4秒前
CiCi完成签到 ,获得积分10
5秒前
苗条秋荷完成签到,获得积分10
5秒前
6秒前
季不住发布了新的文献求助10
6秒前
天道酬勤发布了新的文献求助10
6秒前
6秒前
传奇3应助科研通管家采纳,获得10
6秒前
xfq0829应助科研通管家采纳,获得10
6秒前
6秒前
丘比特应助科研通管家采纳,获得10
6秒前
香蕉觅云应助科研通管家采纳,获得10
6秒前
苒柒发布了新的文献求助10
6秒前
我是牛马应助科研通管家采纳,获得10
6秒前
嘻嘻哈哈应助科研通管家采纳,获得10
7秒前
星辰大海应助无限的香采纳,获得10
7秒前
Orange应助科研通管家采纳,获得30
7秒前
7秒前
7秒前
上官若男应助科研通管家采纳,获得10
7秒前
打打应助科研通管家采纳,获得20
7秒前
所所应助顺利的蘑菇采纳,获得10
7秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Introducing the Learning Sciences 1000
2026年中国辛酸癸酸聚乙二醇甘油酯行业市场现状调查及投资机会研判报告 1000
2026年中国辛酸癸酸聚乙二醇甘油酯行业市场规模及竞争格局分析报告 1000
Resiliency Scale for Adolescents--Chinese Version 800
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
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 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7325216
求助须知:如何正确求助?哪些是违规求助? 8940587
关于积分的说明 18958126
捐赠科研通 6981885
什么是DOI,文献DOI怎么找? 3215601
关于科研通互助平台的介绍 2382830
邀请新用户注册赠送积分活动 2194874