| Literature DB >> 29797227 |
Maria Andrea Barbosa1,2, Renata Guerra-Sá2,3,4, Uberdan Guilherme Mendes De Castro2,4, Wanderson Geraldo de Lima3,4, Robson Augusto Souza Dos Santos2,5, Maria José Campagnole-Santos2,5, Andréia Carvalho Alzamora6,7,8,9.
Abstract
Physical training (PT) has been considered as a treatment in metabolic syndrome (MS), since it induces thermogenic activity in brown (BAT) and white (WAT) adipose tissues. We evaluated the therapeutic effect of PT on activity of WAT and BAT in rats with MS induced by high-fat diet (30% lard) for 13 weeks and submitted, for the last 6 weeks, to swimming or kept sedentary (SED) rats. MS-SED rats compared to control diet (CT-SED) rats showed low physical fitness and high levels of glucose, insulin, homeostasis evaluation of insulin resistance (HOMA-IR), homeostasis evaluation of the functional capacity of β-cells (HOMA-β), and blood pressure. The gastrocnemius muscle decreased in peroxisome proliferator-activated receptor gamma coactivator 1-alpha and beta (PGC-1α, PGC-1β), and uncoupled protein 2 and 3 (UCP2 and UCP3) expressions. Both WAT and BAT increased in the adipocyte area and decreased in blood vessels and fibroblast numbers. WAT increased in expression of pro-inflammatory adipokines and decreased in anti-inflammatory adipokine and adiponectin. WAT and gastrocnemius showed impairment in the insulin signaling pathway. In response to PT, MS rats showed increased physical fitness and restoration of certain biometric and biochemical parameters and blood pressure. PT also induced thermogenic modulations in skeletal muscle, WAT and BAT, and also improved the insulin signaling pathway. Collectively, PT was effective in treating MS by inducing improvement in physical fitness and interchangeable effects between skeletal muscle, WAT and BAT, suggesting a development of brown-like adipocyte cells.Entities:
Keywords: Adipose tissue remodeling; High-fat diet; Insulin signaling pathway; Metabolic syndrome; Physical training; Thermogenesis
Mesh:
Substances:
Year: 2018 PMID: 29797227 DOI: 10.1007/s13105-018-0637-x
Source DB: PubMed Journal: J Physiol Biochem ISSN: 1138-7548 Impact factor: 4.158