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Lipolysis sensation by white fat afferent nerves triggers brown fat thermogenesis
OBJECTIVE: Metabolic challenges, such as a cold environment, stimulate sympathetic neural efferent activity to white adipose tissue (WAT) to drive lipolysis, thereby increasing the availability of free fatty acids as one source of fuel for brown adipose tissue (BAT) thermogenesis. WAT is also innerv...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021673/ https://www.ncbi.nlm.nih.gov/pubmed/27656400 http://dx.doi.org/10.1016/j.molmet.2016.06.013 |
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author | Garretson, John T. Szymanski, Laura A. Schwartz, Gary J. Xue, Bingzhong Ryu, Vitaly Bartness, Timothy J. |
author_facet | Garretson, John T. Szymanski, Laura A. Schwartz, Gary J. Xue, Bingzhong Ryu, Vitaly Bartness, Timothy J. |
author_sort | Garretson, John T. |
collection | PubMed |
description | OBJECTIVE: Metabolic challenges, such as a cold environment, stimulate sympathetic neural efferent activity to white adipose tissue (WAT) to drive lipolysis, thereby increasing the availability of free fatty acids as one source of fuel for brown adipose tissue (BAT) thermogenesis. WAT is also innervated by sensory nerve fibers that network to metabolic brain areas; moreover, activation of these afferents is reported to increase sympathetic nervous system outflow. However, the endogenous stimuli sufficient to drive WAT afferents during metabolic challenges as well as their functional relation to BAT thermogenesis remain unknown. METHOD: We tested if local WAT lipolysis directly activates WAT afferent nerves, and then assessed whether this WAT sensory signal affected BAT thermogenesis in Siberian hamsters (Phodopus sungorus). RESULTS: 2-deoxyglucose, a sympathetic nervous system stimulant, caused β-adrenergic receptor dependent increases in inguinal WAT (IWAT) afferent neurophysiological activity. In addition, direct IWAT injections of the β(3)-AR agonist CL316,243 dose-dependently increased: 1) phosphorylation of IWAT hormone sensitive lipase, an indicator of SNS-stimulated lipolysis, 2) expression of the neuronal activation marker c-Fos in dorsal root ganglion neurons receiving sensory input from IWAT, and 3) IWAT afferent neurophysiological activity, an increase blocked by antilipolytic agent 3,5-dimethylpyrazole. Finally, we demonstrated that IWAT afferent activation by lipolysis triggers interscapular BAT thermogenesis through a neural link between these two tissues. CONCLUSIONS: These data suggest IWAT lipolysis activates local IWAT afferents triggering a neural circuit from WAT to BAT that acutely induces BAT thermogenesis. |
format | Online Article Text |
id | pubmed-5021673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-50216732016-09-21 Lipolysis sensation by white fat afferent nerves triggers brown fat thermogenesis Garretson, John T. Szymanski, Laura A. Schwartz, Gary J. Xue, Bingzhong Ryu, Vitaly Bartness, Timothy J. Mol Metab Original Article OBJECTIVE: Metabolic challenges, such as a cold environment, stimulate sympathetic neural efferent activity to white adipose tissue (WAT) to drive lipolysis, thereby increasing the availability of free fatty acids as one source of fuel for brown adipose tissue (BAT) thermogenesis. WAT is also innervated by sensory nerve fibers that network to metabolic brain areas; moreover, activation of these afferents is reported to increase sympathetic nervous system outflow. However, the endogenous stimuli sufficient to drive WAT afferents during metabolic challenges as well as their functional relation to BAT thermogenesis remain unknown. METHOD: We tested if local WAT lipolysis directly activates WAT afferent nerves, and then assessed whether this WAT sensory signal affected BAT thermogenesis in Siberian hamsters (Phodopus sungorus). RESULTS: 2-deoxyglucose, a sympathetic nervous system stimulant, caused β-adrenergic receptor dependent increases in inguinal WAT (IWAT) afferent neurophysiological activity. In addition, direct IWAT injections of the β(3)-AR agonist CL316,243 dose-dependently increased: 1) phosphorylation of IWAT hormone sensitive lipase, an indicator of SNS-stimulated lipolysis, 2) expression of the neuronal activation marker c-Fos in dorsal root ganglion neurons receiving sensory input from IWAT, and 3) IWAT afferent neurophysiological activity, an increase blocked by antilipolytic agent 3,5-dimethylpyrazole. Finally, we demonstrated that IWAT afferent activation by lipolysis triggers interscapular BAT thermogenesis through a neural link between these two tissues. CONCLUSIONS: These data suggest IWAT lipolysis activates local IWAT afferents triggering a neural circuit from WAT to BAT that acutely induces BAT thermogenesis. Elsevier 2016-06-30 /pmc/articles/PMC5021673/ /pubmed/27656400 http://dx.doi.org/10.1016/j.molmet.2016.06.013 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Garretson, John T. Szymanski, Laura A. Schwartz, Gary J. Xue, Bingzhong Ryu, Vitaly Bartness, Timothy J. Lipolysis sensation by white fat afferent nerves triggers brown fat thermogenesis |
title | Lipolysis sensation by white fat afferent nerves triggers brown fat thermogenesis |
title_full | Lipolysis sensation by white fat afferent nerves triggers brown fat thermogenesis |
title_fullStr | Lipolysis sensation by white fat afferent nerves triggers brown fat thermogenesis |
title_full_unstemmed | Lipolysis sensation by white fat afferent nerves triggers brown fat thermogenesis |
title_short | Lipolysis sensation by white fat afferent nerves triggers brown fat thermogenesis |
title_sort | lipolysis sensation by white fat afferent nerves triggers brown fat thermogenesis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021673/ https://www.ncbi.nlm.nih.gov/pubmed/27656400 http://dx.doi.org/10.1016/j.molmet.2016.06.013 |
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