Literature DB >> 25086779

Green tea extract improves high fat diet-induced hypothalamic inflammation, without affecting the serotoninergic system.

Marcos H Okuda1, Juliane C S Zemdegs2, Aline A de Santana2, Aline B Santamarina2, Mayara F Moreno2, Ana C L Hachul2, Bruno dos Santos2, Claudia M Oller do Nascimento2, Eliane B Ribeiro2, Lila M Oyama2.   

Abstract

To investigate possible mechanisms of green tea's anti-obesity and anti-diabetic effects in the hypothalamus, the central regulator of metabolism, of mice fed with high-fat diet (HFD), we analyzed proteins of the toll-like receptor 4 (TLR4) pathway and serotoninergic proteins involved in energy homeostasis. Thirty-day-old male Swiss mice were fed with HFD rich in saturated fat and green tea extract (GTE) for 8 weeks. After that, body weight and mass of fat depots were evaluated. Oral glucose tolerance test was performed 3 days prior to euthanasia; serum glucose, insulin and adiponectin were measured in fasted mice. Hypothalamic TLR4 pathway proteins, serotonin receptors 1B and 2C and serotonin transporter were analyzed by Western blotting or enzyme-linked immunosorbent assay. A second set of animals was used to measure food intake in response to fluoxetine, a selective serotonin reuptake inhibitor. Mice fed with HFD had increased body weight and mass of fat depots, impaired oral glucose tolerance, elevated glucose and insulin and decreased adiponectin serum levels. TLR4, IκB-α, nuclear factor κB p50 and interleukin 6 were increased by HFD. Concomitant GTE treatment ameliorated these parameters. The serotoninergic system remained functional after HFD treatment despite a few alterations in protein content of serotonin receptors 1B and 2C and serotonin transporter. In summary, the GTE attenuated the deleterious effects of the HFD investigated in this study, partially due to reduced hypothalamic inflammation.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Green tea extract; High-fat diet; Hypothalamus; Neuroinflammation; Serotonin

Mesh:

Substances:

Year:  2014        PMID: 25086779     DOI: 10.1016/j.jnutbio.2014.05.012

Source DB:  PubMed          Journal:  J Nutr Biochem        ISSN: 0955-2863            Impact factor:   6.048


  12 in total

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