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酮色林对大鼠和家兔一侧肾、一侧肾动脉夹闭性肾动脉狭窄早期血管活性物质升压反应的影响。

Effect of ketanserin on pressor response to vasoactive substances in early phase of one-kidney, one clip renal artery stenosis in rats and rabbits.

作者信息

Fujie M, Ichikawa S, Kogure M, Hatakeyama K, Kawajiri S, Murata K

出版信息

Jpn Circ J. 1986 Nov;50(11):1174-80. doi: 10.1253/jcj.50.1174.

DOI:10.1253/jcj.50.1174
PMID:3546768
Abstract

The effect of ketanserin (KET), a specific 5-hydroxytryptamine2 (5-HT2) receptor blockade, on pressor response to vasoactive substances was examined in rats with one-kidney, one clip renal artery stenosis of 2 days' duration (2-day clipped rat) and in rabbits with renal artery stenosis of 3 days' duration (3-day clipped rabbits). The 2-day clipped rats showed hyperresponsiveness to norepinephrine (NE), arginine vasopressin (AVP) and 5-HT. All hyperresponsiveness were attenuated by a subdepressor dose of KET. The infusion of KET, 10 micrograms/kg/min for 30 minutes, decreased mean arterial pressure of the 3-day clipped rabbits; the dose did not alter blood pressure of the normal controls. Exaggerated pressor response to NE was observed in the 3-day clipped rabbits and was abolished by a subdepressor dose of KET, 2.5 micrograms/kg/min. These results suggest that 5-HT may be involved in the enhanced pressor response to vasoconstrictor substances in the 2-day clipped rats and 3-day clipped rabbits, and that it may also play an important role in maintaining blood pressure in the 3-day clipped rabbits.

摘要

在病程为2天的单肾单夹肾动脉狭窄大鼠(2天夹闭大鼠)和病程为3天的肾动脉狭窄家兔(3天夹闭家兔)中,研究了特异性5-羟色胺2(5-HT2)受体阻滞剂酮色林(KET)对血管活性物质升压反应的影响。2天夹闭大鼠对去甲肾上腺素(NE)、精氨酸加压素(AVP)和5-羟色胺表现出反应过度。所有过度反应均被亚降压剂量的KET减弱。以10微克/千克/分钟的剂量输注KET 30分钟,可降低3天夹闭家兔的平均动脉压;该剂量对正常对照的血压无影响。在3天夹闭家兔中观察到对NE的升压反应增强,而2.5微克/千克/分钟的亚降压剂量KET可消除这种反应。这些结果表明,5-羟色胺可能参与了2天夹闭大鼠和3天夹闭家兔对血管收缩物质增强的升压反应,并且它可能在维持3天夹闭家兔的血压中也起重要作用。

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1
Effect of ketanserin on pressor response to vasoactive substances in early phase of one-kidney, one clip renal artery stenosis in rats and rabbits.酮色林对大鼠和家兔一侧肾、一侧肾动脉夹闭性肾动脉狭窄早期血管活性物质升压反应的影响。
Jpn Circ J. 1986 Nov;50(11):1174-80. doi: 10.1253/jcj.50.1174.
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