Ginkgo bilobaExtract Improves Insulin Signaling and Attenuates Inflammation in Retroperitoneal Adipose Tissue Depot of Obese Rats

Author:

Hirata Bruna Kelly Sousa1,Banin Renata Mancini1,Dornellas Ana Paula Segantine2,de Andrade Iracema Senna2,Zemdegs Juliane Costa Silva2,Caperuto Luciana Chagas1,Oyama Lila Missae2,Ribeiro Eliane Beraldi2,Telles Monica Marques1

Affiliation:

1. Departamento de Ciências Biológicas, Universidade Federal de São Paulo (UNIFESP), Rua Arthur Riedel, 275 Eldorado, 09972-270 Diadema, SP, Brazil

2. Departamento de Fisiologia, Disciplina de Fisiologia da Nutrição, Universidade Federal de São Paulo (UNIFESP), Rua Botucatu, 862 Vila Clementino, São Paulo, SP, Brazil

Abstract

Due to the high incidence and severity of obesity and its related disorders, it is highly desirable to develop new strategies to treat or even to prevent its development. We have previously described thatGinkgo bilobaextract (GbE) improved insulin resistance and reduced body weight gain of obese rats. In the present study we aimed to evaluate the effect of GbE on both inflammatory cascade and insulin signaling in retroperitoneal fat depot of diet-induced obese rats. Rats were fed with high fat diet for 2 months and thereafter treated for 14 days with 500 mg/kg of GbE. Rats were then euthanized and samples from retroperitoneal fat depot were used for western blotting, RT-PCR, and ELISA experiments. The GbE treatment promoted a significant reduction on both food/energy intake and body weight gain in comparison to the nontreated obese rats. In addition, a significant increase of both Adipo R1 and IL-10 gene expressions and IR and Akt phosphorylation was also observed, while NF-κB p65 phosphorylation and TNF-αlevels were significantly reduced. Our data suggest that GbE might have potential as a therapy to treat obesity-related metabolic diseases, with special interest to treat obese subjects resistant to adhere to a nutritional education program.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Hindawi Limited

Subject

Cell Biology,Immunology

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