Abstract

Inhibitors of methionine aminopeptidase 2 (MetAP2) have been shown to reduce body weight in obese mice and humans. The target tissue and cellular mechanism of MetAP2 inhibitors, however, have not been extensively examined. Using compounds with diverse chemical scaffolds, we showed that MetAP2 inhibition decreases body weight and fat mass and increases lean mass in the obese mice but not in the lean mice. Obesity is associated with catecholamine resistance and blunted β-adrenergic receptor signaling activities, which could dampen lipolysis and energy expenditure resulting in weight gain. In the current study, we examined effect of MetAP2 inhibition on brown adipose tissue and brown adipocytes. Norepinephrine increases energy expenditure in brown adipose tissue by providing fatty acid substrate through lipolysis and by increasing expression of uncoupled protein-1 (UCP1). Metabolomic analysis shows that in response to MetAP2 inhibitor treatment, fatty acid metabolites in brown adipose tissue increase transiently and subsequently decrease to basal or below basal levels, suggesting an effect on fatty acid metabolism in this tissue. Treatment of brown adipocytes with MetAP2 inhibitors enhances norepinephrine-induced lipolysis and energy expenditure, and prolongs the activity of norepinephrine to increase ucp1 gene expression and energy expenditure in norepinephrine-desensitized brown adipocytes. In summary, we showed that the anti-obesity activity of MetAP2 inhibitors can be mediated, at least in part, through direct action on brown adipocytes by enhancing β-adrenergic-signaling-stimulated activities.

Highlights

  • Inhibitors of methionine aminopeptidase 2 (MetAP2) have been shown to reduce body weight in obese mice and humans

  • Using three chemically different MetAP2 compounds increases the chance that the biological activities observed is because of MetAP2 inhibition and not compound-specific offtarget effect

  • Pretreatment with A357300 or beloranib can increase the ucp1 expression to 88-fold and 177-fold, respectively, at 24 h. These results suggest that MetAP2 inhibition can maintain ucp1 up-regulation after prolonged norepinephrine treatment (Fig. 7D)

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Summary

Results

Inhibitors of methionine aminopeptidase 2 (MetAP2) such as TNP-470 and fumagillin reduced body weight in ob/ob and high-fat diet–induced obese mice [1,2,3,4]. A MetAP2 inhibitor from Zafgen, was shown to cause weight loss in obese humans [5,6,7,8], providing the clinical validation for targeting MetAP2-mediated pathway to treat obesity. Further development of beloranib was discontinued because of adverse effects, The authors declare that they have no conflicts of interest with the contents of this article

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Discussion
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