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Inherently lean rats have enhanced activity and skeletal muscle response to central melanocortin receptors
OBJECTIVE: Activity thermogenesis and energy expenditure (EE) are elevated in intrinsically lean rats (high-capacity runners, HCR), and are also stimulated by melanocortin receptor activation in the ventromedial hypothalamus (VMH). Here, we determined if HCR are more responsive to central modulation...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916025/ https://www.ncbi.nlm.nih.gov/pubmed/29566460 http://dx.doi.org/10.1002/oby.22166 |
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author | Gavini, Chaitanya K. Britton, Steven L. Koch, Lauren G. Novak, Colleen M. |
author_facet | Gavini, Chaitanya K. Britton, Steven L. Koch, Lauren G. Novak, Colleen M. |
author_sort | Gavini, Chaitanya K. |
collection | PubMed |
description | OBJECTIVE: Activity thermogenesis and energy expenditure (EE) are elevated in intrinsically lean rats (high-capacity runners, HCR), and are also stimulated by melanocortin receptor activation in the ventromedial hypothalamus (VMH). Here, we determined if HCR are more responsive to central modulation of activity EE compared to low-capacity runners (LCR). METHODS: HCR and LCR rats received intra-VMH microinjections of Melanotan II (MTII), a mixed melanocortin receptor agonist. Changes in EE, respiratory exchange ratio (RER), activity EE, muscle heat, norepinephrine turnover (NETO), and muscle energetic modulators were compared. RESULTS: HCR were significantly more responsive to intra-VMH MTII-induced changes in EE, activity EE, NETO to some muscle subgroups, and muscle mRNA expression of some energetic modulators. Though HCR had high muscle activity thermogenesis, limited MTII-induced modulation of muscle thermogenesis during activity was seen in LCR only. CONCLUSIONS: An inherently lean, high-capacity rat phenotype showed elevated response to central melanocortin stimulation of activity EE and use of fat as fuel. This may be driven by sympathetic outflow to skeletal muscle, which was elevated after MTII. Central melanocortin receptor activation also altered skeletal muscle energetic modulators in a manner consistent with elevated EE and lowered RER. |
format | Online Article Text |
id | pubmed-5916025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-59160252018-09-22 Inherently lean rats have enhanced activity and skeletal muscle response to central melanocortin receptors Gavini, Chaitanya K. Britton, Steven L. Koch, Lauren G. Novak, Colleen M. Obesity (Silver Spring) Article OBJECTIVE: Activity thermogenesis and energy expenditure (EE) are elevated in intrinsically lean rats (high-capacity runners, HCR), and are also stimulated by melanocortin receptor activation in the ventromedial hypothalamus (VMH). Here, we determined if HCR are more responsive to central modulation of activity EE compared to low-capacity runners (LCR). METHODS: HCR and LCR rats received intra-VMH microinjections of Melanotan II (MTII), a mixed melanocortin receptor agonist. Changes in EE, respiratory exchange ratio (RER), activity EE, muscle heat, norepinephrine turnover (NETO), and muscle energetic modulators were compared. RESULTS: HCR were significantly more responsive to intra-VMH MTII-induced changes in EE, activity EE, NETO to some muscle subgroups, and muscle mRNA expression of some energetic modulators. Though HCR had high muscle activity thermogenesis, limited MTII-induced modulation of muscle thermogenesis during activity was seen in LCR only. CONCLUSIONS: An inherently lean, high-capacity rat phenotype showed elevated response to central melanocortin stimulation of activity EE and use of fat as fuel. This may be driven by sympathetic outflow to skeletal muscle, which was elevated after MTII. Central melanocortin receptor activation also altered skeletal muscle energetic modulators in a manner consistent with elevated EE and lowered RER. 2018-03-22 2018-05 /pmc/articles/PMC5916025/ /pubmed/29566460 http://dx.doi.org/10.1002/oby.22166 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Gavini, Chaitanya K. Britton, Steven L. Koch, Lauren G. Novak, Colleen M. Inherently lean rats have enhanced activity and skeletal muscle response to central melanocortin receptors |
title | Inherently lean rats have enhanced activity and skeletal muscle response to central melanocortin receptors |
title_full | Inherently lean rats have enhanced activity and skeletal muscle response to central melanocortin receptors |
title_fullStr | Inherently lean rats have enhanced activity and skeletal muscle response to central melanocortin receptors |
title_full_unstemmed | Inherently lean rats have enhanced activity and skeletal muscle response to central melanocortin receptors |
title_short | Inherently lean rats have enhanced activity and skeletal muscle response to central melanocortin receptors |
title_sort | inherently lean rats have enhanced activity and skeletal muscle response to central melanocortin receptors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916025/ https://www.ncbi.nlm.nih.gov/pubmed/29566460 http://dx.doi.org/10.1002/oby.22166 |
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