New central targets for the treatment of obesity

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

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.

Publication types

  • Review

MeSH terms

  • Anti-Obesity Agents / pharmacology
  • Anti-Obesity Agents / therapeutic use*
  • Appetite Depressants / therapeutic use*
  • Body Mass Index
  • Body Weight
  • Drug Delivery Systems
  • Energy Metabolism / drug effects*
  • Humans
  • Obesity / drug therapy*
  • Obesity / metabolism
  • Selective Serotonin Reuptake Inhibitors / therapeutic use*
  • Serotonin / metabolism*
  • Weight Loss / drug effects*

Substances

  • Anti-Obesity Agents
  • Appetite Depressants
  • Serotonin Uptake Inhibitors
  • Serotonin