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Am J Physiol Regul Integr Comp Physiol 294: R1968-R1979, 2008. First published April 16, 2008; doi:10.1152/ajpregu.00778.2007
0363-6119/08 $8.00
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SLEEP AND TEMPERATURE REGULATION

Loss of prokineticin receptor 2 signaling predisposes mice to torpor

Preeti H. Jethwa,1 Helen I'Anson,2 Amy Warner,1 Hayden M. Prosser,3 Michael H. Hastings,4 Elizabeth S. Maywood,4 and Francis J. P. Ebling1

1School of Biomedical Sciences, University of Nottingham Medical School, Nottingham; 2Department of Biology, Washington and Lee University, Lexington, Virginia; 3The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge; and 4Medical Research Council Laboratory of Molecular Biology, Neurobiology Division, Cambridge, United Kingdom

Submitted 25 October 2007 ; accepted in final form 10 April 2008

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.

metabolic rate; thermoregulation; CLAMS; radiotelemetry



Address for reprint requests and other correspondence: F. J. P. Ebling, School of Biomedical Sciences, Univ. of Nottingham Medical School, Queen's Medical Centre, Nottingham, NG7 2UH, UK (e-mail: fran.ebling{at}nottingham.ac.uk)







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