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α-肾上腺素能受体药物对压力感受器反射的中枢作用。

Central action of alpha-adrenoceptor agents on the baroreceptor reflex.

作者信息

Ockert D M, Czachurski J, Dembowsky K, Seller H

机构信息

I. Physiologisches Institut, Universität Heidelberg, FRG.

出版信息

J Auton Nerv Syst. 1992 Nov;41(1-2):93-101. doi: 10.1016/0165-1838(92)90131-y.

Abstract

In chloralose-anaesthetized cats the effects of intravenous application of the alpha 1- and alpha 2-adrenoceptor agonistic and antagonistic agents methoxamine, prazosin, B-HT 933 and rauwolscine were tested on baroreceptor reflex, sympathetic background activity and blood pressure. Sympathetic activity was recorded from the renal nerve and the efficacy of the central transmission of the baroreceptor reflex was measured by the duration of the complete inhibition of renal nerve activity during electrical stimulation of the left carotid sinus nerve. All baroreceptors were denervated by sectioning both carotid sinus and vagal nerves. The alpha 1-agonist methoxamine increased baroreceptor-induced sympatho-inhibition, sympathetic background activity and blood pressure. The alpha 1-antagonist prazosin had the opposite effects. The alpha 2-agonist B-HT 933 was most effective in augmenting the inhibitory response in sympathetic activity to baroreceptor stimulation; sympathetic background activity and blood pressure were also decreased. At low doses (50 micrograms/kg) the alpha 2-antagonist rauwolscine reduced the baroreceptor sympathetic reflex inhibition and increased sympathetic activity and blood pressure. The effect of B-HT 933 upon the baroreceptor reflex could be completely antagonized by rauwolscine. These findings demonstrate a very effective facilitation of the baroreceptor reflex transmission by stimulation of central alpha 2-adrenoceptors. Through such humoral-neuronal interaction circulating catecholamines are likely to modulate cardiovascular control.

摘要

在水合氯醛麻醉的猫身上,测试了静脉注射α1和α2肾上腺素能受体激动剂及拮抗剂美托咪定、哌唑嗪、B-HT 933和萝芙辛对压力感受器反射、交感神经基础活动和血压的影响。从肾神经记录交感神经活动,通过电刺激左颈动脉窦神经期间肾神经活动完全抑制的持续时间来测量压力感受器反射的中枢传递效率。通过切断双侧颈动脉窦和迷走神经使所有压力感受器去神经支配。α1激动剂美托咪定增加了压力感受器诱导的交感神经抑制、交感神经基础活动和血压。α1拮抗剂哌唑嗪则产生相反的效果。α2激动剂B-HT 933在增强交感神经活动对压力感受器刺激的抑制反应方面最有效;交感神经基础活动和血压也降低。在低剂量(50微克/千克)时,α2拮抗剂萝芙辛降低了压力感受器交感神经反射抑制,并增加了交感神经活动和血压。B-HT 933对压力感受器反射的作用可被萝芙辛完全拮抗。这些发现表明,刺激中枢α2肾上腺素能受体可非常有效地促进压力感受器反射传递。通过这种体液-神经元相互作用,循环中的儿茶酚胺可能调节心血管控制。

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