Berggren A, Sillén U, Rubenson A
Department of Pediatric Surgery, Ostra sjukhuset, Göteborg, Sweden.
Pharmacol Toxicol. 1991 Jan;68(1):34-8. doi: 10.1111/j.1600-0773.1991.tb01204.x.
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.
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。