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Miglitol protects against age-dependent weight gain in mice: A potential role of increased UCP1 content in brown adipose tissue. | LitMetric

Miglitol protects against age-dependent weight gain in mice: A potential role of increased UCP1 content in brown adipose tissue.

Endocr J

Laboratory of Metabolic Signal, Institute of Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma, 371-8512, Japan.

Published: February 2016

AI Article Synopsis

  • Miglitol is an alpha-glucosidase inhibitor that helps manage post-meal high blood sugar and has been shown to promote healthy fat tissue in mice on high-fat diets.
  • In a new study, miglitol was tested on mice fed a normal diet to see if it could prevent weight gain associated with aging.
  • The results indicated that miglitol could stop age-related weight gain, decrease body fat, and boost energy spending, without affecting how much the mice ate or their activity levels.

Article Abstract

Miglitol is an absorbable alpha-glucosidase inhibitor that is used to control post-prandial hyperglycemia. We previously found that miglitol stimulates brown adipose tissue and prevents diet-induced obesity in mice that are fed a high-fat, high-carbohydrate diet. In this study, we examined whether miglitol can also protect against aging-dependent weight gain in mice that are fed a normal chow diet. Male C57Bl/6J mice were fed normal chow with or without miglitol (800 ppm) for 12 weeks, starting at 12 weeks of age. Food intake and body weight were monitored. After 12 weeks, adiposity, energy expenditure, and locomotor activities were measured. After sacrifice, weight of the epididymal white adipose tissue and adipocyte size were measured. Finally, Ucp1 gene expression and UCP1 protein abundance in brown adipose tissue were quantified by RT-PCR and Western analyses, respectively. Miglitol prevented age-related weight gain without affecting growth of the animals. Miglitol-treated mice showed reduced adiposity and increased oxygen consumption compared to controls, accompanied by higher UCP1 protein abundance in brown adipose tissue. Food intake and locomotor activities were not affected. These results suggest that miglitol can protect against age-dependent weight gain. Elucidating the molecular targets of miglitol in brown adipose tissue and optimizing drug delivery and efficacy may provide new strategies to combat obesity.

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Source
http://dx.doi.org/10.1507/endocrj.EJ15-0116DOI Listing

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