Pharmacological Characterization of GSK573719 (Umeclidinium): A Novel, Long-Acting, Inhaled Antagonist of the Muscarinic Cholinergic Receptors for Treatment of Pulmonary Diseases

毒蕈碱乙酰胆碱受体 毒蕈碱拮抗剂 支气管收缩 异丙托溴铵 卡巴胆碱 药理学 医学 哌仑西平 敌手 效力 阿托品 化学 毒蕈碱乙酰胆碱受体M2 受体 麻醉 内科学 支气管扩张剂 生物化学 体外 气道 哮喘
作者
M Salmon,Mark A. Luttmann,James J. Foley,Peter T. Buckley,Dulcie B. Schmidt,Miriam Burman,Edward F. Webb,Christopher J. DeHaas,Charles J. Kotzer,Victoria J. Barrett,Robert J. Slack,Henry M. Sarau,Michael R. Palovich,Dramane I. Lainé,Douglas W.P. Hay,William L. Rumsey
出处
期刊:Journal of Pharmacology and Experimental Therapeutics [American Society for Pharmacology and Experimental Therapeutics]
卷期号:345 (2): 260-270 被引量:78
标识
DOI:10.1124/jpet.112.202051
摘要

Activation of muscarinic subtype 3 (M3) muscarinic cholinergic receptors (mAChRs) increases airway tone, whereas its blockade improves lung function and quality of life in patients with pulmonary diseases. The present study evaluated the pharmacological properties of a novel mAChR antagonist, GSK573719 (4-[hydroxy(diphenyl)methyl]-1-{2-[(phenylmethyl)oxy]ethyl}-1-azoniabicyclo[2.2.2]octane; umeclidinium). The affinity (Ki) of GSK573719 for the cloned human M1–M5 mAChRs ranged from 0.05 to 0.16 nM. Dissociation of [3H]GSK573719 from the M3 mAChR was slower than that for the M2 mAChR [half-life (t1/2) values: 82 and 9 minutes, respectively]. In Chinese hamster ovary cells transfected with recombinant human M3 mAChRs, GSK573719 demonstrated picomolar potency (–log pA2 = 23.9 pM) in an acetylcholine (Ach)-mediated Ca2+ mobilization assay. Concentration-response curves indicate competitive antagonism with partial reversibility after drug washout. Using isolated human bronchial strips, GSK573719 was also potent and showed competitive antagonism (–log pA2 = 316 pM) versus carbachol, and was slowly reversible in a concentration-dependent manner (1–100 nM). The time to 50% restoration of contraction at 10 nM was about 381 minutes (versus 413 minutes for tiotropium bromide). In mice, the ED50 value was 0.02 μg/mouse intranasally. In conscious guinea pigs, intratracheal administration of GSK573719 dose dependently blocked Ach-induced bronchoconstriction with long duration of action, and was comparable to tiotropium; 2.5 μg elicited 50% bronchoprotection for >24 hours. Thus, GSK573719 is a potent anticholinergic agent that demonstrates slow functional reversibility at the human M3 mAChR and long duration of action in animal models. This pharmacological profile translated into a 24-hour duration of bronchodilation in vivo, which suggested umeclidinium will be a once-daily inhaled treatment of pulmonary diseases.
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
天天快乐应助武文博采纳,获得10
刚刚
研友_RLN4OZ完成签到 ,获得积分10
刚刚
刚刚
willa完成签到,获得积分10
刚刚
谭平完成签到,获得积分10
刚刚
刚刚
彭于晏应助MuMu采纳,获得10
刚刚
hua完成签到 ,获得积分10
刚刚
Jasmine发布了新的文献求助10
1秒前
含糊的蘑菇完成签到 ,获得积分10
1秒前
悦耳寒松完成签到,获得积分10
1秒前
陆陆完成签到 ,获得积分10
1秒前
LIHAO完成签到,获得积分10
1秒前
佐罗完成签到,获得积分10
2秒前
2秒前
2秒前
jie发布了新的文献求助10
3秒前
小二郎应助关关采纳,获得10
3秒前
十五完成签到,获得积分10
3秒前
Y橙子完成签到,获得积分10
3秒前
秉朔完成签到,获得积分10
3秒前
喜欢完成签到,获得积分10
3秒前
思源应助专注乐驹采纳,获得10
3秒前
谭平发布了新的文献求助10
3秒前
Roger完成签到,获得积分10
3秒前
diu完成签到,获得积分10
3秒前
3秒前
满君清完成签到,获得积分10
4秒前
七颗茶香豆应助Ssyong采纳,获得10
4秒前
赘婿应助梦圆采纳,获得10
4秒前
星辰大海应助leslierui采纳,获得10
4秒前
共享精神应助潇洒哥采纳,获得10
4秒前
4秒前
bkagyin应助w7采纳,获得10
4秒前
4秒前
sususu完成签到,获得积分10
5秒前
fullman发布了新的文献求助30
5秒前
开朗清涟完成签到,获得积分10
5秒前
完美世界应助L1nL1n采纳,获得10
5秒前
红3完成签到,获得积分10
5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
Nine new races of Peronospora manshurica found on soybeans in the Midwest 1000
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 600
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Eudora Welty and Modern Media 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7773009
求助须知:如何正确求助?哪些是违规求助? 9315166
关于积分的说明 20343774
捐赠科研通 7358733
什么是DOI,文献DOI怎么找? 3317123
关于科研通互助平台的介绍 2465658
邀请新用户注册赠送积分活动 2332235