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[甲苯磺酸酚妥拉明对下尿路的作用(1)。对离体兔尿道和膀胱的作用]

[Effect of moxisylyte on the lower urinary tracts (1). Effect on the isolated rabbit urethra and bladder].

作者信息

Watanabe K, Hayashi Y, Ikeda K, Ohnishi H

机构信息

Pharmaceuticals Research Laboratories, Fujirebio Inc., Tokyo, Japan.

出版信息

Nihon Yakurigaku Zasshi. 1991 Mar;97(3):145-51. doi: 10.1254/fpj.97.3_145.

Abstract

Effect of moxisylyte on the lower urinary tracts was studied in comparison with those of prazosin and bunazosin in the isolated rabbit bladder and urethra. Moxisylyte dose-dependently inhibited the urethral contraction induced by phenylephrine. The IC50 value of moxisylyte was 1.01 x 10(-6) M. Prazosin and bunazosin inhibited the urethral contraction as well as moxisylyte. The IC50 values of prazosin and bunazosin were 2.88 x 10(-7) M and 1.44 x 10(-7) M, respectively. Moreover, moxisylyte and bunazosin inhibited the urethral contraction induced by KCl. The IC50 values of moxisylyte and bunazosin were 1.17 x 10(-5) M and 1.35 x 10(-4) M, respectively. The KCl/phenylephrine ratios of moxisylyte, bunazosin and prazosin were as follows: 17, 938 and 9201, respectively. Moxisylyte has a relaxant action on the urethra that is probably ascribable to its alpha 1-adrenoceptor antagonist and Ca++ antagonist actions. In the isolated bladder, moxisylyte inhibited the bladder contraction induced by KCl, with an IC50 value of 4.46 x 10(-5) M. However, moxisylyte did not affect the contractile response to acetylcholine. These results suggest that the relaxant effect of moxisylyte on the urethra is due to alpha 1-adrenoceptor antagonist and Ca++ antagonist actions. Therefore, moxisylyte is useful for the therapeutic treatment of micturitional disorder.

摘要

在离体兔膀胱和尿道中,研究了莫西赛利对下尿路的作用,并与哌唑嗪和布那唑嗪进行了比较。莫西赛利剂量依赖性地抑制去氧肾上腺素诱导的尿道收缩。莫西赛利的IC50值为1.01×10⁻⁶M。哌唑嗪和布那唑嗪也抑制尿道收缩。哌唑嗪和布那唑嗪的IC50值分别为2.88×10⁻⁷M和1.44×10⁻⁷M。此外,莫西赛利和布那唑嗪抑制氯化钾诱导的尿道收缩。莫西赛利和布那唑嗪的IC50值分别为1.17×10⁻⁵M和1.35×10⁻⁴M。莫西赛利、布那唑嗪和哌唑嗪的氯化钾/去氧肾上腺素比值如下:分别为17, 938和9201。莫西赛利对尿道有舒张作用,这可能归因于其α1-肾上腺素能受体拮抗剂和Ca²⁺拮抗剂作用。在离体膀胱中,莫西赛利抑制氯化钾诱导的膀胱收缩,IC50值为4.46×10⁻⁵M。然而,莫西赛利不影响对乙酰胆碱的收缩反应。这些结果表明,莫西赛利对尿道的舒张作用是由于α1-肾上腺素能受体拮抗剂和Ca²⁺拮抗剂作用。因此,莫西赛利可用于治疗排尿障碍。

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