Role of paraventricular nucleus in control of blood pressure and drinking in rats
L. L. Jensen, J. W. Harding and J. W. Wright Department of Psychology, Washington State University, Pullman 99164. The present investigation examined the abilities of angiotensin (ANG) II and III to produce increases in blood pressure and drinking when microinfused into the paraventricular nucleus (...
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Veröffentlicht in: | American journal of physiology. Renal physiology 1992-06, Vol.262 (6), p.1068-F1075 |
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Zusammenfassung: | L. L. Jensen, J. W. Harding and J. W. Wright
Department of Psychology, Washington State University, Pullman 99164.
The present investigation examined the abilities of angiotensin (ANG) II
and III to produce increases in blood pressure and drinking when
microinfused into the paraventricular nucleus (PVN) of the hypothalamus of
the Sprague-Dawley rat. Dose-dependent elevations in systemic blood
pressure and heart rate were measured to both ANG II and III in the
anesthetized rat, with ANG II more potent than ANG III at the two highest
doses examined. Pretreatment with the specific ANG receptor antagonist
[Sar1,Thr8]ANG II (sarthran), blocked subsequent ANG II- and III-induced
elevations in blood pressure, suggesting that these responses were
dependent on the activation of ANG receptors. A similar analysis in awake
rats yielded nearly equivalent results. A final experiment demonstrated
that microinfusions of ANG II and III into the PVN produced drinking in a
dose-dependent manner, with greater consumption to ANG II than ANG III.
Again, sarthran was found to block the dipsogenic response. Histological
examination revealed that the location of the injection site was linked to
the character of the ANG-dependent response. These data suggest that the
PVN may play a critical role in mediating central ANG effects on body water
homeostasis and blood pressure regulation. Furthermore, it appears that
subnuclei of the PVN may participate differentially in ANG-mediated
actions. |
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ISSN: | 0363-6127 0002-9513 1931-857X 2161-1157 1522-1466 |
DOI: | 10.1152/ajprenal.1992.262.6.f1068 |