Miller Keith J
Metabolic Diseases Research, HPW 21-2.03, Discovery Biology P.O. Box 5400, Princeton, NJ 08543-5400, USA.
Mol Interv. 2005 Oct;5(5):282-91. doi: 10.1124/mi.5.5.8.
Obesity continues to be a burgeoning health problem worldwide. Before their removal from the market, fenfluramine and the more active enantiomer dexfenfluramine were considered to be among the most effective of weight loss agents. Much of the weight loss produced by fenfluramine was attributed to the direct activation of serotonin 5-HT(2C) receptors in the central nervous system via the desmethyl-metabolite of fenfluramine, norfenfluramine. Norfenfluramine, however, is non-selective, activating additional serotonin receptors, such as 5-HT(2A) and 5-HT(2B), which likely mediated the heart valve hypertrophy seen in many patients. Development of highly selective 5-HT(2C) agonists may recapitulate the clinical anti-obesity properties observed with fenfluramine while avoiding the significant cardiovascular and pulmonary side effects.
肥胖仍然是全球范围内一个不断发展的健康问题。在被撤出市场之前,芬氟拉明以及活性更强的对映体右芬氟拉明被认为是最有效的减肥药物之一。芬氟拉明产生的大部分体重减轻归因于其去甲基代谢产物去甲芬氟拉明对中枢神经系统中5-羟色胺5-HT(2C)受体的直接激活。然而,去甲芬氟拉明具有非选择性,它还会激活其他5-羟色胺受体,如5-HT(2A)和5-HT(2B),这可能是许多患者出现心脏瓣膜肥大的原因。开发高选择性5-HT(2C)激动剂可能重现芬氟拉明所观察到的临床抗肥胖特性,同时避免严重的心血管和肺部副作用。