Hegde S S, Eglen R M
Institute of Pharmacology, Neurobiology Unit, Roche Bioscience, Palo Alto, California 94304, USA.
FASEB J. 1996 Oct;10(12):1398-407. doi: 10.1096/fasebj.10.12.8903510.
The 5-HT4 receptor is a member of the seven transmembrane spanning G-protein-coupled family of receptors. The receptor is positively coupled to adenylate cyclase and exists in two isoforms (5-HT4S and 5-HT4L) that differ in the length and sequence of their carboxy termini. The 5-HT4 receptor is pharmacologically defined by selective agonists such as SC 53116 and RS 67506, and selective antagonists such as GR 113808, SB 204070, and RS 39604. The receptor is widely distributed in the central nervous system and peripheral tissues. In the periphery, the receptor plays an important role in the function of several organ responses including the alimentary tract, urinary bladder, heart and adrenal gland. In the alimentary tract, stimulation of 5-HT4 receptors has a pronounced effect on smooth muscle tone, mucosal electrolyte secretion, and the peristaltic reflex. In the urinary bladder, activation of 5-HT4 receptors modulates cholinergic/purinergic transmission. In the heart, stimulation of atrial 5-HT4 receptors produces positive inotropy and tachycardia that can precipitate arrhythmias. In the adrenal gland, agonism of 5-HT4 receptors stimulates release of cortisol, corticosterone, and aldosterone. Since its discovery in 1988, significant advances have been made in our understanding of the physiology and pharmacology of the 5-HT4 receptor. These advances have led to the development of several selective 5-HT4 receptor agonists and antagonists that may have therapeutic utility in the treatment of peripheral disorders such as irritable bowel syndrome, gastroparesis, urinary incontinence and cardiac arrhythmias.
5-羟色胺4(5-HT4)受体是七跨膜G蛋白偶联受体家族的成员。该受体正向偶联腺苷酸环化酶,存在两种亚型(5-HT4S和5-HT4L),其羧基末端的长度和序列有所不同。5-HT4受体在药理学上由选择性激动剂如SC 53116和RS 67506以及选择性拮抗剂如GR 113808、SB 204070和RS 39604来定义。该受体广泛分布于中枢神经系统和外周组织。在外周,该受体在包括消化道、膀胱、心脏和肾上腺在内的多种器官反应功能中发挥重要作用。在消化道中,刺激5-HT4受体对平滑肌张力、黏膜电解质分泌和蠕动反射有显著影响。在膀胱中,激活5-HT4受体可调节胆碱能/嘌呤能传递。在心脏中,刺激心房5-HT4受体可产生正性肌力作用和心动过速,进而可能引发心律失常。在肾上腺中,5-HT4受体激动可刺激皮质醇、皮质酮和醛固酮的释放。自1988年发现以来,我们对5-HT4受体的生理学和药理学的认识取得了重大进展。这些进展促使开发了几种选择性5-HT4受体激动剂和拮抗剂,它们可能在治疗外周疾病如肠易激综合征、胃轻瘫、尿失禁和心律失常方面具有治疗效用。