Leptin resistance elicits depressive-like behaviors in rats
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.
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Leptin resistance can elicit depressive-like behaviors in rats and is associated with atypical features of depression (increased appetite and weight) in humans.
“leptin resistance can elicit depressive-like behaviors in rats [144] and is associated with atypical features of depression (increased appetite and weight) in humans [145].”
From The menace of obesity to depression and anxiety prevalence (2022) · cites this paper as [144]
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References 47 · Cited by 16
- Authors
- Macht, V. A., Vazquez, M., Petyak, C. E., Grillo, C. A., Kaigler, K., Enos, R. T., McClellan, J. L., Cranford, T. L., Murphy, E. A., Nyland, J. F., Solomon, G., Gertler, A., Wilson, M. A., & Reagan, L. P.
- Affiliations
- University of South Carolina (US)
- Hebrew University of Jerusalem (IL)
- Corresponding author
- Reagan, L.P.
- Venue
- Brain Behavior and Immunity
- Publisher
- Elsevier BV
- Published
- 2017-02
- Volume
- 60
- Pages
- 151-160
- ISSN
- 0889-1591 (ISSN-L)
- OpenAlex
- W2531735597
- Cited by
- 16
- References
- 47
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 2 · 2022: 1 · 2021: 6 · 2020: 2 · 2019: 1 · 2017: 2
- FWCI
- 0.64
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Brain Behavior and Immunity (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Department of Veterans Affairs
- University of South Carolina School of Medicine Research Development Fund
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- leptin resistance, depression-like behavior, obesity, peripheral inflammation, leptin signaling
- MeSH terms
- Animals, Behavior, Animal, Body Weight, Depression, Inflammation, Male, Obesity, Rats, Sprague-Dawley, Leptin
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