| Literature DB >> 27743935 |
V A Macht1, M Vazquez2, C E Petyak2, C A Grillo2, K Kaigler2, R T Enos3, J L McClellan3, T L Cranford3, E A Murphy3, J F Nyland3, G Solomon4, A Gertler4, M A Wilson5, L P Reagan6.
Abstract
There is a growing appreciation that the complications of obesity extend to the central nervous system (CNS) and include increased risk for development of neuropsychiatric co-morbidities such as depressive illness. The neurological consequences of obesity may develop as a continuum and involve a progression of pathological features which is initiated by leptin resistance. Leptin resistance is a hallmark feature of obesity, but it is unknown whether leptin resistance or blockage of leptin action is casually linked to the neurological changes which underlie depressive-like phenotypes. Accordingly, the aim of the current study was to examine whether chronic administration of a pegylated leptin receptor antagonist (Peg-LRA) elicits depressive-like behaviors in adult male rats. Peg-LRA administration resulted in endocrine and metabolic features that are characteristic of an obesity phenotype. Peg-LRA rats also exhibited increased immobility in the forced swim test, depressive-like behaviors that were accompanied by indices of peripheral inflammation. These results demonstrate that leptin resistance elicits an obesity phenotype that is characterized by peripheral immune changes and depressive-like behaviors in rats, supporting the concept that co-morbid obesity and depressive illness develop as a continuum resulting from changes in the peripheral endocrine and metabolic milieu. Published by Elsevier Inc.Entities:
Keywords: Activated T cells; Adiposity; C-reactive protein; Forced swim test; Inflammation; Obesity; Pegylated leptin receptor antagonist; Spleen; Triglycerides
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Year: 2016 PMID: 27743935 DOI: 10.1016/j.bbi.2016.10.008
Source DB: PubMed Journal: Brain Behav Immun ISSN: 0889-1591 Impact factor: 7.217