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内毒素血症清醒大鼠体内的血管紧张素 II、血管加压素及交感神经活动

Angiotensin II, vasopressin, and sympathetic activity in conscious rats with endotoxemia.

作者信息

Schaller M D, Waeber B, Nussberger J, Brunner H R

出版信息

Am J Physiol. 1985 Dec;249(6 Pt 2):H1086-92. doi: 10.1152/ajpheart.1985.249.6.H1086.

DOI:10.1152/ajpheart.1985.249.6.H1086
PMID:3907375
Abstract

The role of the sympathetic nervous system, angiotensin II (ANG II), and arginine vasopressin (AVP) in maintaining blood pressure (BP) during endotoxic shock was investigated in 117 conscious male Wistar rats. After intravenous injection of 2 mg Escherichia coli endotoxin, mean BP fell within 5 min by approximately 50 mmHg and rose again to approach base-line levels within 90 min. At that time, plasma renin activity, plasma norepinephrine (NE), and vasopressin levels of the endotoxin-treated animals were, respectively, 12-, 10-, and 54-fold (P less than 0.001) higher than those of the controls. The BP effect of either prazosin (0.125 mg iv), captopril (2.5 mg iv), or d(CH2)5Tyr(Me)AVP (5 micrograms iv), a specific antagonist of the vascular effect of AVP, was evaluated over a 30-min observation period starting 90 min after administration of endotoxin or its vehicle. Captopril reduced mean BP from 116 +/- 1.8 to a low of 109 +/- 2.1 (SE) mmHg (P less than 0.05, n = 8) only in rats pretreated with endotoxin, whereas the vasopressin antagonist had no depressor effect even during endotoxemia. The BP drop induced by prazosin in rats exposed to endotoxin (-21 +/- 3.3 mmHg, n = 6) did not significantly differ from that observed in control rats (-14 +/- 3.4 mmHg, n = 6). A dose-response curve to NE, ANG II, and lysine vasopressin was also performed. In endotoxin-treated rats the mean BP response to all agonists was markedly suppressed (P less than 0.001).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在117只清醒雄性Wistar大鼠中研究了交感神经系统、血管紧张素II(ANG II)和精氨酸加压素(AVP)在内毒素休克期间维持血压(BP)的作用。静脉注射2mg大肠杆菌内毒素后,平均血压在5分钟内下降约50mmHg,并在90分钟内再次上升至接近基线水平。此时,内毒素处理动物的血浆肾素活性、血浆去甲肾上腺素(NE)和加压素水平分别比对照组高12倍、10倍和54倍(P<0.001)。在内毒素或其赋形剂给药90分钟后开始的30分钟观察期内,评估了哌唑嗪(0.125mg静脉注射)、卡托普利(2.5mg静脉注射)或d(CH2)5Tyr(Me)AVP(5μg静脉注射,一种AVP血管效应的特异性拮抗剂)对血压的影响。卡托普利仅在内毒素预处理的大鼠中使平均血压从116±1.8降至最低109±2.1(SE)mmHg(P<0.05,n=8),而加压素拮抗剂即使在内毒素血症期间也没有降压作用。哌唑嗪对内毒素处理大鼠引起的血压下降(-21±3.3mmHg,n=6)与对照大鼠中观察到的(-14±3.4mmHg,n=6)没有显著差异。还进行了对NE、ANG II和赖氨酸加压素的剂量反应曲线研究。在内毒素处理的大鼠中,对所有激动剂的平均血压反应均明显受到抑制(P<0.001)。(摘要截断于250字)

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