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膀胱平滑肌的反应机制。

Mechanisms of reactivity of urinary bladder smooth muscle.

作者信息

Mokry J, Svihra J, Nosalova G, Kliment J

机构信息

Department of Pharmacology, Jessenius Faculty of Medicine, Comenius University, Martin, Slovakia.

出版信息

Bratisl Lek Listy. 2002;103(9):279-82.

Abstract

BACKGROUND

Mechanism of bladder smooth muscle contraction and relaxation and its pharmacological influence in various pathologic states are of incremental interest of investigators and clinicians.

OBJECTIVES

The aim of our study was to assess the reactivity of urinary bladder smooth muscle in guinea pigs to two different pharmacological agents.

METHODS

We compared the in vitro reactivity of smooth muscle strips of guinea pig urinary bladder to muscarinic stimulation by carbachol and acetylcholine. We prepared two kinds of strips, urothelium-denuded and with intact urothelium. Both kinds of strips were aerated under tension in Krebs-Henseleit's solution in organ-bath for 1 hour and after that cumulative concentration-response curves to carbachol (10(-9) - 10(-5) mol/l) and acetylcholine (10(-8) - 10(-3) mol/l) were constructed.

RESULTS

We observed significantly higher reactivity of smooth muscle strips to carbachol, comparing to acetylcholine at the same concentrations both in strips with urothelium (at concentration 10(-5) mol/l: 22.1 g/100 mg vs 6.1 g/100 mg) and in urothelium-denuded strips (at concentration 10(-5) mol/l: 24.5 g/100 mg vs 5.1 g/100 mg). The reactivity differences between strips with and without urothelium were not significant, however, in higher concentrations of acetylcholine (10(-4) and 10(-5) mol/l) and carbachol (10(-6) and 10(-5) mol/l) we noticed no significant inhibition of contractile response of smooth muscle strips with intact urothelium.

CONCLUSION

In our experiments we confirmed that carbachol was more potent constrictor than acetylcholine in detrusor smooth muscle strips of guinea pigs. The presence of urothelium did not change the reactivity significantly. (Fig. 4, Ref: 23.).

摘要

背景

膀胱平滑肌收缩与舒张机制及其在各种病理状态下的药理学影响,日益受到研究者和临床医生的关注。

目的

本研究旨在评估豚鼠膀胱平滑肌对两种不同药理试剂的反应性。

方法

我们比较了豚鼠膀胱平滑肌条对卡巴胆碱和乙酰胆碱毒蕈碱刺激的体外反应性。我们制备了两种条带,即去上皮条带和上皮完整条带。两种条带均在器官浴中的克雷布斯 - 亨泽莱特溶液中于张力下通气1小时,之后构建对卡巴胆碱(10^(-9) - 10^(-5) mol/l)和乙酰胆碱(10^(-8) - 10^(-3) mol/l)的累积浓度 - 反应曲线。

结果

我们观察到,在相同浓度下,无论是上皮完整的条带(在浓度10^(-5) mol/l时:22.1 g/100 mg对6.1 g/100 mg)还是去上皮条带(在浓度10^(-5) mol/l时:24.5 g/100 mg对5.1 g/100 mg),平滑肌条对卡巴胆碱的反应性均显著高于对乙酰胆碱的反应性。然而,在较高浓度的乙酰胆碱(10^(-4)和10^(-5) mol/l)和卡巴胆碱(10^(-6)和10^(-5) mol/l)下,我们注意到上皮完整的平滑肌条带的收缩反应没有受到显著抑制。

结论

在我们的实验中,我们证实卡巴胆碱在豚鼠逼尿肌平滑肌条带中比乙酰胆碱是更强效的收缩剂。上皮的存在并没有显著改变反应性。(图4,参考文献:23。)

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