Cargando…

S6K1 in the Central Nervous System Regulates Energy Expenditure via MC4R/CRH Pathways in Response to Deprivation of an Essential Amino Acid

It is well established that the central nervous system (CNS), especially the hypothalamus, plays an important role in regulating energy homeostasis and lipid metabolism. We have previously shown that hypothalamic corticotropin-releasing hormone (CRH) is critical for stimulating fat loss in response...

Descripción completa

Detalles Bibliográficos
Autores principales: Xia, Tingting, Cheng, Ying, Zhang, Qian, Xiao, Fei, Liu, Bin, Chen, Shanghai, Guo, Feifan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447917/
https://www.ncbi.nlm.nih.gov/pubmed/22787141
http://dx.doi.org/10.2337/db11-1278
_version_ 1782244194642821120
author Xia, Tingting
Cheng, Ying
Zhang, Qian
Xiao, Fei
Liu, Bin
Chen, Shanghai
Guo, Feifan
author_facet Xia, Tingting
Cheng, Ying
Zhang, Qian
Xiao, Fei
Liu, Bin
Chen, Shanghai
Guo, Feifan
author_sort Xia, Tingting
collection PubMed
description It is well established that the central nervous system (CNS), especially the hypothalamus, plays an important role in regulating energy homeostasis and lipid metabolism. We have previously shown that hypothalamic corticotropin-releasing hormone (CRH) is critical for stimulating fat loss in response to dietary leucine deprivation. The molecular mechanisms underlying the CNS regulation of leucine deprivation–stimulated fat loss are, however, still largely unknown. Here, we used intracerebroventricular injection of adenoviral vectors to identify a novel role for hypothalamic p70 S6 kinase 1 (S6K1), a major downstream effector of the kinase mammalian target of rapamycin, in leucine deprivation stimulation of energy expenditure. Furthermore, we show that the effect of hypothalamic S6K1 is mediated by modulation of Crh expression in a melanocortin-4 receptor–dependent manner. Taken together, our studies provide a new perspective for understanding the regulation of energy expenditure by the CNS and the importance of cross-talk between nutritional control and regulation of endocrine signals.
format Online
Article
Text
id pubmed-3447917
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher American Diabetes Association
record_format MEDLINE/PubMed
spelling pubmed-34479172013-10-01 S6K1 in the Central Nervous System Regulates Energy Expenditure via MC4R/CRH Pathways in Response to Deprivation of an Essential Amino Acid Xia, Tingting Cheng, Ying Zhang, Qian Xiao, Fei Liu, Bin Chen, Shanghai Guo, Feifan Diabetes Metabolism It is well established that the central nervous system (CNS), especially the hypothalamus, plays an important role in regulating energy homeostasis and lipid metabolism. We have previously shown that hypothalamic corticotropin-releasing hormone (CRH) is critical for stimulating fat loss in response to dietary leucine deprivation. The molecular mechanisms underlying the CNS regulation of leucine deprivation–stimulated fat loss are, however, still largely unknown. Here, we used intracerebroventricular injection of adenoviral vectors to identify a novel role for hypothalamic p70 S6 kinase 1 (S6K1), a major downstream effector of the kinase mammalian target of rapamycin, in leucine deprivation stimulation of energy expenditure. Furthermore, we show that the effect of hypothalamic S6K1 is mediated by modulation of Crh expression in a melanocortin-4 receptor–dependent manner. Taken together, our studies provide a new perspective for understanding the regulation of energy expenditure by the CNS and the importance of cross-talk between nutritional control and regulation of endocrine signals. American Diabetes Association 2012-10 2012-09-13 /pmc/articles/PMC3447917/ /pubmed/22787141 http://dx.doi.org/10.2337/db11-1278 Text en © 2012 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Metabolism
Xia, Tingting
Cheng, Ying
Zhang, Qian
Xiao, Fei
Liu, Bin
Chen, Shanghai
Guo, Feifan
S6K1 in the Central Nervous System Regulates Energy Expenditure via MC4R/CRH Pathways in Response to Deprivation of an Essential Amino Acid
title S6K1 in the Central Nervous System Regulates Energy Expenditure via MC4R/CRH Pathways in Response to Deprivation of an Essential Amino Acid
title_full S6K1 in the Central Nervous System Regulates Energy Expenditure via MC4R/CRH Pathways in Response to Deprivation of an Essential Amino Acid
title_fullStr S6K1 in the Central Nervous System Regulates Energy Expenditure via MC4R/CRH Pathways in Response to Deprivation of an Essential Amino Acid
title_full_unstemmed S6K1 in the Central Nervous System Regulates Energy Expenditure via MC4R/CRH Pathways in Response to Deprivation of an Essential Amino Acid
title_short S6K1 in the Central Nervous System Regulates Energy Expenditure via MC4R/CRH Pathways in Response to Deprivation of an Essential Amino Acid
title_sort s6k1 in the central nervous system regulates energy expenditure via mc4r/crh pathways in response to deprivation of an essential amino acid
topic Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447917/
https://www.ncbi.nlm.nih.gov/pubmed/22787141
http://dx.doi.org/10.2337/db11-1278
work_keys_str_mv AT xiatingting s6k1inthecentralnervoussystemregulatesenergyexpenditureviamc4rcrhpathwaysinresponsetodeprivationofanessentialaminoacid
AT chengying s6k1inthecentralnervoussystemregulatesenergyexpenditureviamc4rcrhpathwaysinresponsetodeprivationofanessentialaminoacid
AT zhangqian s6k1inthecentralnervoussystemregulatesenergyexpenditureviamc4rcrhpathwaysinresponsetodeprivationofanessentialaminoacid
AT xiaofei s6k1inthecentralnervoussystemregulatesenergyexpenditureviamc4rcrhpathwaysinresponsetodeprivationofanessentialaminoacid
AT liubin s6k1inthecentralnervoussystemregulatesenergyexpenditureviamc4rcrhpathwaysinresponsetodeprivationofanessentialaminoacid
AT chenshanghai s6k1inthecentralnervoussystemregulatesenergyexpenditureviamc4rcrhpathwaysinresponsetodeprivationofanessentialaminoacid
AT guofeifan s6k1inthecentralnervoussystemregulatesenergyexpenditureviamc4rcrhpathwaysinresponsetodeprivationofanessentialaminoacid