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Strategies and potential molecular targets for obesity treatment.肥胖治疗的策略及潜在分子靶点
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本文引用的文献

1
Cardiovascular Consequences of Obesity and Targets for Treatment.肥胖的心血管后果及治疗靶点
Drug Discov Today Ther Strateg. 2008;5(1):53-61. doi: 10.1016/j.ddstr.2008.07.001.
2
5-HT2CRs expressed by pro-opiomelanocortin neurons regulate energy homeostasis.促阿片黑素细胞皮质素神经元表达的5-羟色胺2C受体调节能量平衡。
Neuron. 2008 Nov 26;60(4):582-9. doi: 10.1016/j.neuron.2008.09.033.
3
Brain effects of melanocortins.黑皮质素对大脑的影响。
Pharmacol Res. 2009 Jan;59(1):13-47. doi: 10.1016/j.phrs.2008.10.005. Epub 2008 Oct 17.
4
Central control of body weight and appetite.体重与食欲的中枢控制
J Clin Endocrinol Metab. 2008 Nov;93(11 Suppl 1):S37-50. doi: 10.1210/jc.2008-1630.
5
Effect of tesofensine on bodyweight loss, body composition, and quality of life in obese patients: a randomised, double-blind, placebo-controlled trial.替索芬辛对肥胖患者体重减轻、身体成分及生活质量的影响:一项随机、双盲、安慰剂对照试验
Lancet. 2008 Nov 29;372(9653):1906-1913. doi: 10.1016/S0140-6736(08)61525-1. Epub 2008 Oct 22.
6
Gut hormones and appetite control.肠道激素与食欲控制。
Oral Dis. 2009 Jan;15(1):18-26. doi: 10.1111/j.1601-0825.2008.01492.x. Epub 2008 Oct 17.
7
Sleep and metabolism: shared circuits, new connections.睡眠与新陈代谢:共享回路,新的联系。
Trends Endocrinol Metab. 2008 Dec;19(10):362-70. doi: 10.1016/j.tem.2008.08.007. Epub 2008 Oct 18.
8
CB(1) receptor antagonism: biological basis for metabolic effects.大麻素1型(CB(1))受体拮抗作用:代谢效应的生物学基础
Drug Discov Today. 2008 Dec;13(23-24):1026-41. doi: 10.1016/j.drudis.2008.09.001. Epub 2008 Oct 15.
9
Novel functions of orexigenic hypothalamic peptides: from genes to behavior.促食欲下丘脑肽的新功能:从基因到行为
Nutrition. 2008 Sep;24(9):843-7. doi: 10.1016/j.nut.2008.06.028.
10
A critical review of the cannabinoid receptor as a drug target for obesity management.对大麻素受体作为肥胖管理药物靶点的批判性综述。
Obes Rev. 2009 Jan;10(1):58-67. doi: 10.1111/j.1467-789X.2008.00520.x. Epub 2008 Aug 20.

肥胖治疗的新中枢靶点。

New central targets for the treatment of obesity.

机构信息

Discovery R & D, AMRI, Albany, NY 12212, USA.

出版信息

Br J Clin Pharmacol. 2009 Dec;68(6):852-60. doi: 10.1111/j.1365-2125.2009.03550.x.

DOI:10.1111/j.1365-2125.2009.03550.x
PMID:20002079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2810796/
Abstract

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.

摘要

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。