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Hypothalamic IKKbeta/NF-kappaB and ER stress link overnutrition to energy imbalance and obesity
Overnutrition is associated with chronic inflammation in metabolic tissues. Whether metabolic inflammation compromises the neural regulatory systems and therefore promotes overnutrition-associated diseases remains unexplored. Here we show that a mediator of metabolic inflammation, IKKbeta/NF-kappaB,...
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Published in: | Cell 2008-10, Vol.135 (1), p.61-73 |
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container_title | Cell |
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creator | Zhang, Xiaoqing Zhang, Guo Zhang, Hai Karin, Michael Bai, Hua Cai, Dongsheng |
description | Overnutrition is associated with chronic inflammation in metabolic tissues. Whether metabolic inflammation compromises the neural regulatory systems and therefore promotes overnutrition-associated diseases remains unexplored. Here we show that a mediator of metabolic inflammation, IKKbeta/NF-kappaB, normally remains inactive although enriched in hypothalamic neurons. Overnutrition atypically activates hypothalamic IKKbeta/NF-kappaB at least in part through elevated endoplasmic reticulum stress in the hypothalamus. While forced activation of hypothalamic IKKbeta/NF-kappaB interrupts central insulin/leptin signaling and actions, site- or cell-specific suppression of IKKbeta either broadly across the brain or locally within the mediobasal hypothalamus, or specifically in hypothalamic AGRP neurons significantly protects against obesity and glucose intolerance. The molecular mechanisms involved include regulation by IKKbeta/NF-kappaB of SOCS3, a core inhibitor of insulin and leptin signaling. Our results show that the hypothalamic IKKbeta/NF-kappaB program is a general neural mechanism for energy imbalance underlying obesity and suggest that suppressing hypothalamic IKKbeta/NF-kappaB may represent a strategy to combat obesity and related diseases. |
doi_str_mv | 10.1016/j.cell.2008.07.043 |
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Whether metabolic inflammation compromises the neural regulatory systems and therefore promotes overnutrition-associated diseases remains unexplored. Here we show that a mediator of metabolic inflammation, IKKbeta/NF-kappaB, normally remains inactive although enriched in hypothalamic neurons. Overnutrition atypically activates hypothalamic IKKbeta/NF-kappaB at least in part through elevated endoplasmic reticulum stress in the hypothalamus. While forced activation of hypothalamic IKKbeta/NF-kappaB interrupts central insulin/leptin signaling and actions, site- or cell-specific suppression of IKKbeta either broadly across the brain or locally within the mediobasal hypothalamus, or specifically in hypothalamic AGRP neurons significantly protects against obesity and glucose intolerance. The molecular mechanisms involved include regulation by IKKbeta/NF-kappaB of SOCS3, a core inhibitor of insulin and leptin signaling. Our results show that the hypothalamic IKKbeta/NF-kappaB program is a general neural mechanism for energy imbalance underlying obesity and suggest that suppressing hypothalamic IKKbeta/NF-kappaB may represent a strategy to combat obesity and related diseases.</abstract><cop>United States</cop><pmid>18854155</pmid><doi>10.1016/j.cell.2008.07.043</doi><tpages>13</tpages></addata></record> |
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subjects | Agouti-Related Protein - genetics Agouti-Related Protein - metabolism Animals Endoplasmic Reticulum - metabolism Energy Metabolism Humans Hypothalamus - immunology Hypothalamus - physiopathology I-kappa B Proteins - metabolism Immunity, Innate Insulin Resistance Mice Mice, Inbred C57BL Neurons - metabolism NF-kappa B - metabolism Obesity - metabolism Overnutrition - physiopathology Signal Transduction Suppressor of Cytokine Signaling 3 Protein Suppressor of Cytokine Signaling Proteins - metabolism |
title | Hypothalamic IKKbeta/NF-kappaB and ER stress link overnutrition to energy imbalance and obesity |
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