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向最后区微量注射血管加压素和血管紧张素II的心血管后果。

Cardiovascular consequences of microinjection of vasopressin and angiotensin II in the area postrema.

作者信息

Lowes V L, McLean L E, Kasting N W, Ferguson A V

机构信息

Department of Physiology, Queen's University, Kingston, Ontario, Canada.

出版信息

Am J Physiol. 1993 Sep;265(3 Pt 2):R625-31. doi: 10.1152/ajpregu.1993.265.3.R625.

DOI:10.1152/ajpregu.1993.265.3.R625
PMID:8214157
Abstract

Microinjection of angiotensin II (ANG II) into the area postrema (AP) of urethan-anesthetized male Sprague-Dawley rats elicited statistically significant increases in mean arterial blood pressure at doses ranging from 10 pg to 500 ng (10 pg, mean +/- SE, 10.8 +/- 1.1 mmHg, P < 0.001; 250 ng, 15.2 +/- 2.6 mmHg, P < 0.001). Heart rate was also significantly increased at doses > 10 pg, although these increases were not dose dependent. Systemic administration of losartan (Dup-753), an AT1 antagonist, was able to significantly reduce the pressor response to 250 ng ANG (post-losartan: 81.9 +/- 9.5% reduction in blood pressure response, P < 0.0001), whereas PD123319, an AT2 antagonist, was without significant effect (P > 0.1). Microinjection of vasopressin (VP) (10 pg-500 ng) into the AP also resulted in statistically significant increases in blood pressure at doses ranging from 10 to 100 pg (10 pg, 7.0 +/- 1.5 mmHg, P < 0.05) and 100-500 ng (250 ng, 12.2 +/- 1.8 mmHg, P < 0.0001). Small but significant changes in heart rate were observed only at 100 pg and 100 ng. Systemic administration of a V1 antagonist significantly attenuated the increases in blood pressure in response to 50, 100, and 250 ng VP (250 ng, post-V1 antagonist: 66.4 +/- 8.6% reduction in blood pressure response, P < 0.001), whereas [desamino,D-Arg8]vasopressin (DDAVP), a V2 agonist, had a depressor effect when microinjected directly into the AP (250 ng, -9.9 +/- 1.6 mmHg, P < 0.005).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

向经乌拉坦麻醉的雄性斯普拉格-道利大鼠的最后区(AP)微量注射血管紧张素II(ANG II),剂量范围为10皮克至500纳克时,平均动脉血压出现具有统计学意义的升高(10皮克时,均值±标准误,10.8±1.1毫米汞柱,P<0.001;250纳克时,15.2±2.6毫米汞柱,P<0.001)。剂量>10皮克时心率也显著增加,尽管这些增加不依赖于剂量。全身性给予AT1拮抗剂氯沙坦(Dup-753)能够显著降低对250纳克ANG的升压反应(氯沙坦给药后:血压反应降低81.9±9.5%,P<0.0001),而AT2拮抗剂PD123319则无显著作用(P>0.1)。向AP微量注射加压素(VP)(10皮克 - 500纳克),剂量范围为10至100皮克(10皮克时,7.0±1.5毫米汞柱,P<0.05)和100 - 500纳克(250纳克时,12.2±1.8毫米汞柱,P<0.0001)时,血压也出现具有统计学意义的升高。仅在100皮克和100纳克时观察到心率有微小但显著的变化。全身性给予V1拮抗剂可显著减弱对50、100和250纳克VP的血压升高反应(250纳克时,V1拮抗剂给药后:血压反应降低66.4±8.6%,P<0.001),而V2激动剂[去氨基,D-精氨酸8]加压素(DDAVP)直接微量注射到AP时具有降压作用(250纳克时,-9.9±1.6毫米汞柱,P<0.005)。(摘要截选至250字)

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