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Loss of prokineticin receptor 2 signaling predisposes mice to torpor

Jethwa, Preeti H.; I'Anson, Helen; Warner, Amy; Prosser, Hayden M.; Hastings, Michael H.; Maywood, Elizabeth S.; Ebling, Francis J.P.

Authors

Helen I'Anson

Amy Warner

Hayden M. Prosser

Michael H. Hastings

Elizabeth S. Maywood

Francis J.P. Ebling



Abstract

The genes encoding prokineticin 2 polypeptide (Prok2) and its cognate receptor (Prokr2/Gpcr73l1) are widely expressed in both the suprachiasmatic nucleus and its hypothalamic targets, and this signaling pathway has been implicated in the circadian regulation of behavior and physiology. We have previously observed that the targeted null mutation of Prokr2 disrupts circadian coordination of cycles of locomotor activity and thermoregulation. We have now observed spontaneous but sporadic bouts of torpor in the majority of these transgenic mice lacking Prokr2 signaling. During these torpor bouts, which lasted for up to 8 h, body temperature and locomotor activity decreased markedly. Oxygen consumption and carbon dioxide production also decreased, and there was a decrease in respiratory quotient. These spontaneous torpor bouts generally began toward the end of the dark phase or in the early light phase when the mice were maintained on a 12:12-h light-dark cycle and persisted when mice were exposed to continuous darkness. Periods of food deprivation (16-24 h) induced a substantial decrease in body temperature in all mice, but the duration and depth of hypothermia was significantly greater in mice lacking Prokr2 signaling compared with heterozygous and wild-type littermates. Likewise, when tested in metabolic cages, food deprivation produced greater decreases in oxygen consumption and carbon dioxide production in the transgenic mice than controls. We conclude that Prokr2 signaling plays a role in hypothalamic regulation of energy balance, and loss of this pathway results in physiological and behavioral responses normally only detected when mice are in negative energy balance. Copyright © 2008 the American Physiological Society.

Citation

Jethwa, P. H., I'Anson, H., Warner, A., Prosser, H. M., Hastings, M. H., Maywood, E. S., & Ebling, F. J. (2008). Loss of prokineticin receptor 2 signaling predisposes mice to torpor. AJP - Regulatory, Integrative and Comparative Physiology, 294(6), R1968-R1979. https://doi.org/10.1152/ajpregu.00778.2007

Journal Article Type Article
Acceptance Date Apr 10, 2008
Online Publication Date Jun 1, 2008
Publication Date Jun 1, 2008
Deposit Date Jun 25, 2021
Journal American Journal of Physiology - Regulatory Integrative and Comparative Physiology
Print ISSN 0363-6119
Electronic ISSN 1522-1490
Publisher American Physiological Society
Peer Reviewed Peer Reviewed
Volume 294
Issue 6
Pages R1968-R1979
DOI https://doi.org/10.1152/ajpregu.00778.2007
Public URL https://nottingham-repository.worktribe.com/output/3158435
Publisher URL https://journals.physiology.org/doi/full/10.1152/ajpregu.00778.2007