反激动剂
受体
兴奋剂
5-HT1受体
部分激动剂
G蛋白偶联受体
5-HT2受体
5-羟色胺受体
5-HT7受体
药理学
血清素
神经科学
生物
代谢受体
医学
内科学
作者
Joël Bockaert,Sylvie Claeysen,Valérie Compan,Aline Dumuis
标识
DOI:10.1016/j.neuropharm.2008.05.013
摘要
Twenty years ago, we started the characterization of a 5-HT receptor coupled to cAMP production in neurons. This receptor obviously had a different pharmacology to the other 5-HT receptors described at that time, i.e. the 5-HT1, 5-HT2, 5-HT3 receptors. We proposed to name it the 5-HT4 receptor. Nowadays, 5-HT4 receptors are one of the most studied GPCRs belonging to the "rhodopsin" family. Thanks to the existence of a great variety of ligands with inverse agonist, partial agonist, agonist and antagonist profiles, the pharmacological and physiological properties of this receptor are beginning to emerge. Although some 5-HT4 partial agonists have been on the market for gastro-intestinal pathologies, 5-HT4 receptor drugs have still to be commercialized for brain disorders. However, since 5-HT4 receptors have recognized effects on memory, depression and feeding in animal models, there is still hope for a therapeutic destiny of this interesting target in brain disorders.
科研通智能强力驱动
Strongly Powered by AbleSci AI