布美他尼
氯噻嗪
药理学
速尿
协同运输机
利尿剂
化学
利尿剂
氢氯噻嗪
内分泌学
内科学
生物
医学
钠
有机化学
血压
作者
Yuhua Yang,Angela Fu,Xiaosu Wu,Jeff D. Reagan
出处
期刊:Pharmacology
[S. Karger AG]
日期:2012-01-01
卷期号:89 (1-2): 13-17
被引量:31
摘要
We report that the loop diuretic drugs bumetanide and furosemide used in the treatment of hypertension are GPR35 agonists. We utilized calcium flux, inositol phosphate accumulation, and dynamic redistribution assays to examine the pharmacology of these compounds on the human, mouse and rat GPR35. While potent on human GPR35, neither bumetanide nor furosemide were active against mouse or rat GPR35. Furthermore, the Na<sup>+</sup>-Cl<sup>–</sup> cotransporter inhibi- tors chlorothiazide and hydrochlorothiazide were inactive against GPR35 in all three species. We also demonstrate that GPR35 is expressed in human skin where it has been shown that loop diuretics inhibit histamine-induced flare and itch response. These findings suggest that GPR35 may play an important role in skin cell biology and be a potential target for the treatment of a variety of immune disorders.
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