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Acta Physiologica 2007; Volume 191, Supplement 658
Joint Meeting of The Slovak Physiological Society, The Physiological Society and The Federation of European Physiological Societies
9/11/2007-9/14/2007
Bratislava, Slovakia
CLOCK GENES AND RHYTHMIC FUNCTION OF THE CARDIOVASCULAR SYSTEM IN RATS
Abstract number: STH10-48
Zeman1 M., Monosikova1 J., Petrak2 J., Kovacikova1 Z., Mravec2 B., Krizanova3 O., Kvetnansky2 R., Herichova1 I.
1Department of Animal Physiology and Ethology, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia
2Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia
3Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences, Bratislava, Slovakia; [email protected]
The cardiovascular system exhibits distinct circadian rhythms in its activity, mainly in blood pressure (BP), heart rate, peripheral resistance etc. Moreover, number of cardiovascular incidents follows a daily rhythm with maximum risk in the morning hours. It is expected that compromised cardiovascular anticipation observed during hypertension and diabetes can lead to higher risk of cardiovascular incidents. The circadian system plays a key role in anticipation of periodic loads from the environment. Circadian expression of clock gene in the master biological clocks localized in the suprachiasmatic nuclei (SCN) of the hypothalamus and in peripheral organs is important for coordinated function of different organs. In our study we determined daily rhythms in clock genes (per2, Bmal1, clock) expression in target organs (heart and kidney) and central brain structures involved in control of the cardiovascular system (SCN, paraventricular nucleus (n), dorsomedial n., n. ambigus, medulla caudalis ventrolateralis, n. tractus solitarii and circumventricular organs, the anteroventral third ventricle and area postrema). As animals models we used rats with streptozotocine induced diabetes and hypertensive rats TGR(mREN-27) with up regulated renin angiotensine system (RAS) exhibiting a "non dipping" BP profile. Our data suggest that up regulated RAS is important for "non dipping" profile of BP. Mechanisms down stream from the SCN are important for the BP rhythmicity but existence of distinct population of angiotensine II sensitive neurons in the SCN that control BP is still not excluded.
Research was supported by grants APVV-20-022704
To cite this abstract, please use the following information:
Acta Physiologica 2007; Volume 191, Supplement 658 :STH10-48