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Diurnal regulation of metabolism by G(s)-alpha in hypothalamic QPLOT neurons
Neurons in the hypothalamic preoptic area (POA) regulate multiple homeostatic processes, including thermoregulation and sleep, by sensing afferent input and modulating sympathetic nervous system output. The POA has an autonomous circadian clock and may also receive circadian signals indirectly from...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159165/ https://www.ncbi.nlm.nih.gov/pubmed/37141220 http://dx.doi.org/10.1371/journal.pone.0284824 |
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author | Gaitonde, Kevin D. Andrabi, Mutahar Burger, Courtney A. D’Souza, Shane P. Vemaraju, Shruti Koritala, Bala S. C. Smith, David F. Lang, Richard A. |
author_facet | Gaitonde, Kevin D. Andrabi, Mutahar Burger, Courtney A. D’Souza, Shane P. Vemaraju, Shruti Koritala, Bala S. C. Smith, David F. Lang, Richard A. |
author_sort | Gaitonde, Kevin D. |
collection | PubMed |
description | Neurons in the hypothalamic preoptic area (POA) regulate multiple homeostatic processes, including thermoregulation and sleep, by sensing afferent input and modulating sympathetic nervous system output. The POA has an autonomous circadian clock and may also receive circadian signals indirectly from the suprachiasmatic nucleus. We have previously defined a subset of neurons in the POA termed QPLOT neurons that are identified by the expression of molecular markers (Qrfp, Ptger3, LepR, Opn5, Tacr3) that suggest receptivity to multiple stimuli. Because Ptger3, Opn5, and Tacr3 encode G-protein coupled receptors (GPCRs), we hypothesized that elucidating the G-protein signaling in these neurons is essential to understanding the interplay of inputs in the regulation of metabolism. Here, we describe how the stimulatory G(s)-alpha subunit (Gnas) in QPLOT neurons regulates metabolism in mice. We analyzed Opn5(cre); Gnas(fl/fl) mice using indirect calorimetry at ambient temperatures of 22°C (a historical standard), 10°C (a cold challenge), and 28°C (thermoneutrality) to assess the ability of QPLOT neurons to regulate metabolism. We observed a marked decrease in nocturnal locomotion of Opn5(cre); Gnas(fl/fl) mice at both 28°C and 22°C, but no overall differences in energy expenditure, respiratory exchange, or food and water consumption. To analyze daily rhythmic patterns of metabolism, we assessed circadian parameters including amplitude, phase, and MESOR. Loss-of-function GNAS in QPLOT neurons resulted in several subtle rhythmic changes in multiple metabolic parameters. We observed that Opn5(cre); Gnas(fl/fl) mice show a higher rhythm-adjusted mean energy expenditure at 22°C and 10°C, and an exaggerated respiratory exchange shift with temperature. At 28°C, Opn5(cre); Gnas(fl/fl) mice have a significant delay in the phase of energy expenditure and respiratory exchange. Rhythmic analysis also showed limited increases in rhythm-adjusted means of food and water intake at 22°C and 28°C. Together, these data advance our understanding of G(αs)-signaling in preoptic QPLOT neurons in regulating daily patterns of metabolism. |
format | Online Article Text |
id | pubmed-10159165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-101591652023-05-05 Diurnal regulation of metabolism by G(s)-alpha in hypothalamic QPLOT neurons Gaitonde, Kevin D. Andrabi, Mutahar Burger, Courtney A. D’Souza, Shane P. Vemaraju, Shruti Koritala, Bala S. C. Smith, David F. Lang, Richard A. PLoS One Research Article Neurons in the hypothalamic preoptic area (POA) regulate multiple homeostatic processes, including thermoregulation and sleep, by sensing afferent input and modulating sympathetic nervous system output. The POA has an autonomous circadian clock and may also receive circadian signals indirectly from the suprachiasmatic nucleus. We have previously defined a subset of neurons in the POA termed QPLOT neurons that are identified by the expression of molecular markers (Qrfp, Ptger3, LepR, Opn5, Tacr3) that suggest receptivity to multiple stimuli. Because Ptger3, Opn5, and Tacr3 encode G-protein coupled receptors (GPCRs), we hypothesized that elucidating the G-protein signaling in these neurons is essential to understanding the interplay of inputs in the regulation of metabolism. Here, we describe how the stimulatory G(s)-alpha subunit (Gnas) in QPLOT neurons regulates metabolism in mice. We analyzed Opn5(cre); Gnas(fl/fl) mice using indirect calorimetry at ambient temperatures of 22°C (a historical standard), 10°C (a cold challenge), and 28°C (thermoneutrality) to assess the ability of QPLOT neurons to regulate metabolism. We observed a marked decrease in nocturnal locomotion of Opn5(cre); Gnas(fl/fl) mice at both 28°C and 22°C, but no overall differences in energy expenditure, respiratory exchange, or food and water consumption. To analyze daily rhythmic patterns of metabolism, we assessed circadian parameters including amplitude, phase, and MESOR. Loss-of-function GNAS in QPLOT neurons resulted in several subtle rhythmic changes in multiple metabolic parameters. We observed that Opn5(cre); Gnas(fl/fl) mice show a higher rhythm-adjusted mean energy expenditure at 22°C and 10°C, and an exaggerated respiratory exchange shift with temperature. At 28°C, Opn5(cre); Gnas(fl/fl) mice have a significant delay in the phase of energy expenditure and respiratory exchange. Rhythmic analysis also showed limited increases in rhythm-adjusted means of food and water intake at 22°C and 28°C. Together, these data advance our understanding of G(αs)-signaling in preoptic QPLOT neurons in regulating daily patterns of metabolism. Public Library of Science 2023-05-04 /pmc/articles/PMC10159165/ /pubmed/37141220 http://dx.doi.org/10.1371/journal.pone.0284824 Text en © 2023 Gaitonde et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Gaitonde, Kevin D. Andrabi, Mutahar Burger, Courtney A. D’Souza, Shane P. Vemaraju, Shruti Koritala, Bala S. C. Smith, David F. Lang, Richard A. Diurnal regulation of metabolism by G(s)-alpha in hypothalamic QPLOT neurons |
title | Diurnal regulation of metabolism by G(s)-alpha in hypothalamic QPLOT neurons |
title_full | Diurnal regulation of metabolism by G(s)-alpha in hypothalamic QPLOT neurons |
title_fullStr | Diurnal regulation of metabolism by G(s)-alpha in hypothalamic QPLOT neurons |
title_full_unstemmed | Diurnal regulation of metabolism by G(s)-alpha in hypothalamic QPLOT neurons |
title_short | Diurnal regulation of metabolism by G(s)-alpha in hypothalamic QPLOT neurons |
title_sort | diurnal regulation of metabolism by g(s)-alpha in hypothalamic qplot neurons |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159165/ https://www.ncbi.nlm.nih.gov/pubmed/37141220 http://dx.doi.org/10.1371/journal.pone.0284824 |
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