journal article Jan 14, 2015

Leptin resistance in diet‐induced obesity: the role of hypothalamic inflammation

Obesity Reviews Vol. 16 No. 3 pp. 207-224 · Wiley
View at Publisher Save 10.1111/obr.12243
Abstract
SummaryThe consumption of Western diets, high in sugar and saturated fat, is a crucial contributor to the alarming incidence of obesity and its associated morbidities. These diets have been reported to induce an inflammatory response in the hypothalamus, which promotes the development of central leptin resistance and obesity. This inflammatory signalling involves dynamic changes in the expression and activity of several mediators of the innate immune system, including toll‐like receptor 4, IκB kinase‐β/nuclear factor‐κB, c‐Jun N‐terminal kinase, suppressor of cytokine signalling 3 and pro‐inflammatory cytokines, as well as the induction of endoplasmic reticulum stress and autophagy defect. Although the exact cellular mechanisms remain incompletely understood, recent evidence suggests that the inflammatory response is at least mediated by interactions between neurons and non‐neuronal cells such as microglia and astrocytes. Current evidence of the contribution of each inflammatory mediator to leptin resistance and diet‐induced obesity (DIO), including their reciprocal interactions and cell‐type‐specific effects, is reviewed and integrated in a conceptual model. Based upon this model and pharmacological intervention studies, several inflammatory mediators are proposed to be promising therapeutic targets for the treatment of DIO.
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Metrics
186
Citations
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References
Details
Published
Jan 14, 2015
Vol/Issue
16(3)
Pages
207-224
License
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Funding
STW Award: 12264
Cite This Article
K. C. G. de Git, R. A. H. Adan (2015). Leptin resistance in diet‐induced obesity: the role of hypothalamic inflammation. Obesity Reviews, 16(3), 207-224. https://doi.org/10.1111/obr.12243