| Literature DB >> 28710665 |
Vitor Rosetto Muñoz1, Rafael Calais Gaspar1, Barbara Moreira Crisol1, Guilherme Pedron Formigari2, Marcella Ramos Sant'Ana2, José Diego Botezelli1, Rodrigo Stellzer Gaspar1, Adelino S R da Silva3,4, Dennys Esper Cintra2,5, Leandro Pereira de Moura1,5,6, Eduardo Rochete Ropelle1,5,6, José Rodrigo Pauli7,8,9.
Abstract
The present study evaluated the effects of exercise training on pyruvate carboxylase protein (PCB) levels in hepatic tissue and glucose homeostasis control in obese mice. Swiss mice were distributed into three groups: control mice (CTL), fed a standard rodent chow; diet-induced obesity (DIO), fed an obesity-inducing diet; and a third group, which also received an obesity-inducing diet, but was subjected to an exercise training protocol (DIO + EXE). Protocol training was carried out for 1 h/d, 5 d/wk, for 8 weeks, performed at an intensity of 60% of exhaustion velocity. An insulin tolerance test (ITT) was performed in the last experimental week. Twenty-four hours after the last physical exercise session, the animals were euthanized and the liver was harvested for molecular analysis. Firstly, DIO mice showed increased epididymal fat and serum glucose and these results were accompanied by increased PCB and decreased p-Akt in hepatic tissue. On the other hand, physical exercise was able to increase the performance of the mice and attenuate PCB levels and hyperglycemia in DIO + EXE mice. The above findings show that physical exercise seems to be able to regulate hyperglycemia in obese mice, suggesting the participation of PCB, which was enhanced in the obese condition and attenuated after a treadmill running protocol. This is the first study to be aimed at the role of exercise training in hepatic PCB levels, which may be a novel mechanism that can collaborate to reduce the development of hyperglycemia and type 2 diabetes in DIO mice.Entities:
Keywords: Hyperglycemia; Obesity; PCB; Physical exercise; Type 2 diabetes
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Year: 2017 PMID: 28710665 DOI: 10.1007/s12576-017-0559-3
Source DB: PubMed Journal: J Physiol Sci ISSN: 1880-6546 Impact factor: 2.781