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α-1肾上腺素能受体阻滞剂布那唑嗪对去甲肾上腺素诱导的兔近端尿道平滑肌收缩的作用。

Actions of the alpha-1 adrenoceptor blocker bunazosin on the norepinephrine-induced contraction of smooth muscles in the rabbit proximal urethra.

作者信息

Kimoto Y, Nozaki M, Itoh T

出版信息

J Pharmacol Exp Ther. 1987 Jun;241(3):1017-22.

PMID:2885405
Abstract

Effects of bunazosin on the norepinephrine-induced electrical and mechanical activities of smooth muscles of the rabbit proximal urethra were investigated using microelectrode and tension recording methods. Responses to norepinephrine were mediated by activation of both alpha-1 and beta adrenoceptors. In the presence of propranolol, the norepinephrine-induced contraction increased and, with yohimbine, the phasic but not tonic contraction was only inhibited slightly. Contributions of the alpha-2 adrenoceptor to the norepinephrine-induced contraction were negligible. Bunazosin inhibited in a concentration-dependent manner both the phasic and tonic responses of the norepinephrine-induced contraction, and the concentration-response relationship for norepinephrine shifted to the right. The Schild plot obtained from measurements of tonic responses in this antagonism yielded a straight line with a slope of 0.96. The pA2 value for bunazosin was 8.39 and the KB value was 4.1 nM. Prazosin had similar effects (the corresponding values being 0.96, 8.21 and 6.2 nM, respectively). The mechanical response evoked by field stimulation was composed of cholinergic, noradrenergic alpha-1 and noncholinergic-nonadrenergic contractions and of a subsequent nonadrenergic-noncholinergic relaxation. Bunazosin inhibited the twitch contraction evoked by field stimulation more than did prazosin, albeit not completely. These results indicate that although the smooth muscle tone in the urethra is regulated by multiple neural factors, the elevation of the tone is regulated predominantly by activation of the alpha-1 adrenoceptors. Bunazosin has an antagonistic action on this receptor. The actions of bunazosin are discussed in relation to the clinical application in cases of inadequate micturition.

摘要

采用微电极和张力记录方法,研究了布那唑嗪对去甲肾上腺素诱导的兔近端尿道平滑肌电活动和机械活动的影响。对去甲肾上腺素的反应是由α-1和β肾上腺素能受体的激活介导的。在普萘洛尔存在的情况下,去甲肾上腺素诱导的收缩增强,而育亨宾仅轻微抑制相性收缩而非紧张性收缩。α-2肾上腺素能受体对去甲肾上腺素诱导的收缩作用可忽略不计。布那唑嗪以浓度依赖性方式抑制去甲肾上腺素诱导收缩的相性和紧张性反应,去甲肾上腺素的浓度-反应关系向右移动。在此拮抗作用中,通过测量紧张性反应得到的Schild图呈斜率为0.96的直线。布那唑嗪的pA2值为8.39,KB值为4.1 nM。哌唑嗪有类似作用(相应值分别为0.96、8.21和6.2 nM)。场刺激诱发的机械反应由胆碱能、去甲肾上腺素能α-1和非胆碱能-非去甲肾上腺素能收缩以及随后的非肾上腺素能-非胆碱能舒张组成。布那唑嗪比哌唑嗪更能抑制场刺激诱发的抽搐收缩,尽管不完全抑制。这些结果表明,尽管尿道平滑肌张力受多种神经因素调节,但张力升高主要由α-1肾上腺素能受体的激活调节。布那唑嗪对该受体有拮抗作用。结合排尿不足病例的临床应用对布那唑嗪的作用进行了讨论。

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