Suppr超能文献

洛哌丁胺对大鼠膀胱的运动效应:一项体外研究。

Motor effects of loperamide on rat urinary bladder: an in vitro study.

作者信息

Berggren A, Sillén U, Rubenson A

机构信息

Department of Pediatric Surgery, Ostra sjukhuset, Göteborg, Sweden.

出版信息

Pharmacol Toxicol. 1991 Jan;68(1):34-8. doi: 10.1111/j.1600-0773.1991.tb01204.x.

Abstract

Motility recordings in muscle strips from rat urinary bladder were performed and the effect of the opiate agonist loperamide on motor activity was studied. Loperamide induced a concentration-dependent (10(-7)-10(-3) M) inhibition of the contractile response of the detrusor strip of the same order of magnitude after activation of intramural nerves, stimulation of cholinergic receptors with acetylcholine and after direct depolarisation of the cell with potassium. Pretreatment with the opiate-antagonist naloxone (10(-5) M) did not antagonise the inhibitory action of loperamide on bladder motility regardless of the type of activation. Naloxone per se, however, facilitated the nerve-mediated motor response. The inhibitory action of loperamide on the potassium-induced contraction could partly be counteracted by elevation of the calcium concentration in the medium. It is suggested that the demonstrated inhibitory effect of loperamide on bladder motility is a calcium-dependent direct smooth muscle action, without any significant opiate-receptor-mediated action in the present in vitro preparation.

摘要

对大鼠膀胱肌肉条进行了运动记录,并研究了阿片类激动剂洛哌丁胺对运动活性的影响。洛哌丁胺在激活壁内神经、用乙酰胆碱刺激胆碱能受体以及用钾直接使细胞去极化后,诱导了浓度依赖性(10^(-7)-10^(-3)M)的膀胱逼尿肌条收缩反应抑制,其抑制程度相同。无论激活类型如何,用阿片类拮抗剂纳洛酮(10^(-5)M)预处理均不能拮抗洛哌丁胺对膀胱运动的抑制作用。然而,纳洛酮本身促进了神经介导的运动反应。洛哌丁胺对钾诱导收缩的抑制作用可部分通过提高培养基中的钙浓度来抵消。提示洛哌丁胺对膀胱运动的抑制作用是一种钙依赖性的直接平滑肌作用,在目前的体外实验中没有任何明显的阿片受体介导的作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验