[7-D-ALA]-ANGIOTENSIN-(1-7) - SELECTIVE ANTAGONISM OF ANGIOTENSIN-(1-7) IN THE RAT PARAVENTRICULAR NUCLEUS

被引:52
作者
AMBUHL, P
FELIX, D
KHOSLA, MC
机构
[1] UNIV BERN, DIV NEUROBIOL, CH-3012 BERN, SWITZERLAND
[2] CLEVELAND CLIN FDN, RES INST,DEPT NEUROSCI, CLEVELAND, OH 44195 USA
关键词
ANGIOTENSIN II; ANGIOTENSIN-(1-7); PARAVENTRICULAR NUCLEUS; ANGIOTENSIN ANTAGONISM; IONTOPHORESIS; RATS;
D O I
10.1016/0361-9230(94)90103-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Microiontophoretic application of both, the octapeptide angiotensin II (Ang II) and its N-terminal heptapeptide angiotensin-(1-7), [Ang-(1-7)], has been shown to increase the firing rate of rat hypothalamic paraventricular neurones. In the present microiontophoretic study, the effect of the angiotensin analogue [7-D-Ala]-Ang-(1-7) on Ang II- and Ang-(1-7)-induced firing rate increase of paraventricular neurones has been tested. While the response to Ang II was unchanged, the response to Ang-(1-7) was effectively blocked by [7-D-Ala]-Ang-(1-7). The results indicate that the Ang-(1-7)-induced excitation of paraventricular neurones may be mediated by a distinct Ang-(1-7)-receptor and that [7-D-Ala]-Ang-(1-7) is a selective antagonist of this receptor.
引用
收藏
页码:289 / 291
页数:3
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