Angiotensin receptor binding and pressor effects in cat subretrofacial nucleus
A. M. Allen, R. A. Dampney and F. A. Mendelsohn Department of Medicine, University of Melbourne, Austin Hospital, Heidelberg, Victoria. Central administration of angiotensin II (ANG II) increases arterial blood pressure via increased sympathetic activity. We have examined the possibility that one si...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 1988-11, Vol.255 (5), p.H1011-H1017 |
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Sprache: | eng |
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Zusammenfassung: | A. M. Allen, R. A. Dampney and F. A. Mendelsohn
Department of Medicine, University of Melbourne, Austin Hospital, Heidelberg, Victoria.
Central administration of angiotensin II (ANG II) increases arterial blood
pressure via increased sympathetic activity. We have examined the
possibility that one site of action of ANG II is the subretrofacial (SRF)
nucleus in the rostral ventrolateral medulla, since this nucleus is known
to play a critical role in the tonic and phasic control of arterial
pressure. In vitro autoradiography, employing 125I-labeled [Sar1, Ile8]ANG
II as radioligand, was used to localize binding sites for ANG II in the cat
ventrolateral medulla. A high density of ANG II-receptor binding sites was
found confined to the SRF nucleus. In a second group of experiments in
anesthetized cats, microinjections of ANG II, in doses ranging from 10 to
50 pmol, were made into histologically identified sites within and outside
the SRF nucleus. Microinjections into the nucleus resulted in a
dose-dependent increase in arterial pressure, which was abolished by
systemic administration of the ganglion-blocking drug hexamethonium
bromide. In contrast, microinjections just outside the SRF nucleus had no
effect on arterial pressure. It is concluded that activation of ANG
II-receptor binding sites within the SRF nucleus leads to an increase in
arterial pressure via increased sympathetic efferent activity. |
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ISSN: | 0363-6135 0002-9513 1522-1539 2163-5773 |
DOI: | 10.1152/ajpheart.1988.255.5.H1011 |