AJP - Regu Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Am J Physiol Regul Integr Comp Physiol (November 21, 2007). doi:10.1152/ajpregu.00667.2007
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
294/2/R344    most recent
00667.2007v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bechtold, D. A
Right arrow Articles by Piggins, H. D
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bechtold, D. A
Right arrow Articles by Piggins, H. D
Submitted on September 14, 2007
Accepted on November 20, 2007

Metabolic rhythm abnormalities in mice lacking VIP-VPAC2 signaling

David A Bechtold1, Timothy M. Brown2, Simon M Luckman3, and Hugh D Piggins2*

1 Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom; 3.18 Stopford building, manchester, m13 9pt, United Kingdom
2 Faculty of Life Sciences, University of Manchester, Manchester, United Kingdom
3 Faculty of Life Sciences, university of Manchester, Manchester, England, United Kingdom

* To whom correspondence should be addressed. E-mail: hugh.piggins{at}manchester.ac.uk.

The circadian pacemaker in the suprachiasmatic nuclei (SCN) controls endogenous near 24h physiological and behavioral rhythms in metabolism, neuroendocrine function, and locomotor activity. Recently we showed that vasoactive intestinal polypeptide (VIP) and its receptor, VPAC2 are critical to the intercellular communication between individual SCN neurons, and appropriate synchronization and phasing of these oscillatory cells. Mice defective in VIP signaling manifest grossly impaired circadian rhythms of SCN neuronal firing activity, and are typically unable to maintain rhythmic wheel-running behavior in the absence of external time cues. Here we report that daily rhythms of metabolism and feeding behavior are also overtly altered in these animals. Under diurnal conditions (12 h light, 12 h dark, LD), metabolic and feeding rhythms are advanced in mice lacking either VIP or VPAC2 receptor expression, peaking in the late day, rather than early night as observed in wild-type mice. When placed in constant light (LL), both VIP-deficient and VPAC2 receptor-knockout mice exhibit dampening of metabolic and feeding rhythms, which deteriorate after a few days. In addition, overall metabolic rate is greatly reduced in VPAC2-knockout mice, when compared with wild-type mice, regardless of lighting condition. The advancement of metabolic and feeding rhythms in these mice under LD suggests that these rhythms are less sensitive to masking by light. These results demonstrate that altering SCN function not only affects neuronal and wheel-running activity rhythms, but also dramatically impairs temporal regulation of metabolism and feeding.




This article has been cited by other articles:


Home page
J Biol RhythmsHome page
A.T.L. Hughes and H.D. Piggins
Behavioral Responses of Vipr2-/- Mice to Light
J Biol Rhythms, June 1, 2008; 23(3): 211 - 219.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 2007 by the American Physiological Society.