Discovery R & D, AMRI, Albany, NY 12212, USA.
Br J Clin Pharmacol. 2009 Dec;68(6):852-60. doi: 10.1111/j.1365-2125.2009.03550.x.
The review focuses on the central neuronal circuits involved in energy homeostasis and the opportunities these offer for pharmacological intervention to decrease feeding behaviour and reduce weight. This article is based on the presentation 'New central targets for the treatment of obesity' (Sargent, British Pharmacological society, Clinical Section Symposium, December 2008). Central neuronal substrates controlling weight offer numerous opportunities for pharmacological intervention. These opportunities range from non-specific enhancement of monoamine signalling (triple reuptake inhibitors) to targeting specific monoamine receptor subtypes (5-HT(2c) and 5-HT(6)). The data reviewed suggest that these approaches will lead to weight loss; whether this is sufficient to produce clinically meaningful effect remains to be determined. Combination therapy targeting more than one mechanism may be a means of increasing the magnitude of the response. Preclinical studies also suggest that novel approaches targeting specific neuronal pathways within the hypothalamus, e.g. MCH(1) receptor antagonism, offer an opportunity for weight reduction. However, these approaches are at an early stage and clinical studies will be needed to determine if these novel approaches lead to clinically meaningful weight loss and improvements in co-morbid conditions such as diabetes and cardiovascular disorders.
这篇综述主要关注参与能量平衡的中枢神经元回路,以及这些回路为减少摄食行为和减轻体重提供的药理学干预机会。本文基于“肥胖治疗的新中枢靶点”(Sargent,英国药理学会临床分会研讨会,2008 年 12 月)的演讲。控制体重的中枢神经元基质为药理学干预提供了众多机会。这些机会从非特异性增强单胺信号(三重再摄取抑制剂)到靶向特定单胺受体亚型(5-HT(2c)和 5-HT(6))不等。综述的数据表明,这些方法将导致体重减轻;但这是否足以产生临床有意义的效果还有待确定。针对多种机制的联合治疗可能是增加反应幅度的一种手段。针对下丘脑特定神经元通路的新方法(例如 MCH(1)受体拮抗剂)的临床前研究也提供了减轻体重的机会。然而,这些方法还处于早期阶段,需要进行临床研究来确定这些新方法是否会导致临床有意义的体重减轻,并改善糖尿病和心血管疾病等合并症。