AJP - Regu Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Regul Integr Comp Physiol 290: R1122-R1127, 2006. First published December 8, 2005; doi:10.1152/ajpregu.00703.2005
0363-6119/06 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
290/4/R1122    most recent
00703.2005v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 ISI Web of Science (1)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Campos, L. A.
Right arrow Articles by Baltatu, O. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Campos, L. A.
Right arrow Articles by Baltatu, O. C.

SLEEP AND TEMPERATURE REGULATION

Altered circadian rhythm reentrainment to light phase shifts in rats with low levels of brain angiotensinogen

Luciana A. Campos,1,2 Ralph Plehm,1 José Cipolla-Neto,3 Michael Bader,1 and Ovidiu C. Baltatu1,2

1Max-Delbrück-Center for Molecular Medicine, Berlin-Buch, Germany; 2Institute of Research and Development, University of Paraiba Valley, São Jose dos Campos, Brazil; and 3Department of Physiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil

Submitted 3 October 2005 ; accepted in final form 3 December 2005

In this study, we aimed to investigate the adaptation of blood pressure (BP), heart rate (HR), and locomotor activity (LA) circadian rhythms to light cycle shift in transgenic rats with a deficit in brain angiotensin [TGR(ASrAOGEN)]. BP, HR, and LA were measured by telemetry. After baseline recordings (bLD), the light cycle was inverted by prolonging the light by 12 h and thereafter the dark period by 12 h, resulting in inverted dark-light (DL) or light-dark (LD) cycles. Toward that end, a 24-h dark was maintained for 14 days (free-running conditions). When light cycle was changed from bLD to DL, the acrophases (peak time of curve fitting) of BP, HR, and LA shifted to the new dark period in both SD and TGR(ASrAOGEN) rats. However, the readjustment of the BP and HR acrophases in TGR(ASrAOGEN) rats occurred significantly slower than SD rats. The LA acrophases changed similarly in both strains. When light cycle was changed from DL to LD by prolonging the dark period by 12 h, the reentrainment of BP and LA occurred faster than the previous shift in both strains. The readjustment of the BP and HR acrophases in TGR(ASrAOGEN) rats occurred significantly slower than SD rats. In free-running conditions, the circadian rhythms of the investigated parameters adapted in TGR(ASrAOGEN) and SD rats in a similar manner. These results demonstrate that the brain RAS plays an important role in mediating the effects of light cycle shifts on the circadian variation of BP and HR. The adaptive behavior of cardiovascular circadian rhythms depends on the initial direction of light-dark changes.

brain renin-angiotensin system; heart rate



Address for reprint requests and other correspondence: O. C. Baltatu, Institute of Research and Development, Univ. of Paraiba Valley, Av. Shishima Hifumi, 2911, São Jose dos Campos, São Paulo, Brazil 12244–000 (e-mail: ocbaltatu{at}univap.br/ocbaltatu{at}yahoo.com)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2006 by the American Physiological Society.