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β3-肾上腺素能受体在人输尿管中的表达和功能作用。

Expression and functional role of β3 -adrenoceptors in the human ureter.

机构信息

Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Japan.

出版信息

Int J Urol. 2013 Oct;20(10):1007-14. doi: 10.1111/iju.12093. Epub 2013 Jan 29.

Abstract

OBJECTIVES

To investigate the presence of β-adrenoceptor subtypes in the human ureter, and to examine whether β(3) -adrenoceptors modulate relaxation of the human ureter.

METHODS

Expression of messenger ribonucleic acid of β-adrenoceptors in the human ureter was determined by reverse transcription polymerase chain reaction, and distribution of β-adrenoceptors was examined by immunohistochemistry. In functional studies, the relaxant effects of isoproterenol, procaterol, TRK-380, salbutamol and BRL 37344 on KCl-induced contraction of the human ureter were evaluated, and the inhibitory effects of isoproterenol, procaterol and TRK-380 on electrical field stimulation-induced contractions were determined.

RESULTS

Expression of β(1) -, β(2) - and β(3) -adrenoceptor messenger ribonucleic acid in the human ureter was confirmed by reverse transcription polymerase chain reaction. Positive staining for β(1) -, β(2) - and β(3) -adrenoceptor was identified not only in smooth muscle, but also in the urothelium of the human ureter. All β-adrenoceptor agonists decreased the tone of KCl-induced contractions of the human ureter with a rank order of relaxant effects of isoproterenol > procaterol > TRK-380 > salbutamol > BRL 37344. Furthermore, isoproterenol, procaterol and TRK-380 significantly decreased the amplitude of electrical field stimulation-induced contractions with a rank order of inhibitory effects of isoproterenol > procaterol > TRK-380.

CONCLUSIONS

Human ureteral relaxation is mediated by both β(2) - and β(3) -adrenoceptor stimulation. β(3) -Adrenoceptor agonists have the potential to relax the human ureter, and their clinical application in the treatment of ureteral stones is expected.

摘要

目的

研究人输尿管中β-肾上腺素能受体亚型的存在,并探讨β(3)-肾上腺素受体是否调节人输尿管的松弛。

方法

通过反转录聚合酶链反应确定人输尿管中β-肾上腺素能受体信使核糖核酸的表达,并通过免疫组织化学检查β-肾上腺素能受体的分布。在功能研究中,评估了异丙肾上腺素、丙卡特罗、TRK-380、沙丁胺醇和 BRL 37344对 KCl 诱导的人输尿管收缩的松弛作用,并确定了异丙肾上腺素、丙卡特罗和 TRK-380 对电刺激诱导收缩的抑制作用。

结果

通过反转录聚合酶链反应证实了人输尿管中β(1)-、β(2)-和β(3)-肾上腺素能受体信使核糖核酸的表达。β(1)-、β(2)-和β(3)-肾上腺素能受体的阳性染色不仅在平滑肌中,而且在人输尿管的尿路上皮中均有发现。所有β-肾上腺素能受体激动剂均降低 KCl 诱导的人输尿管收缩的张力,松弛作用的顺序为异丙肾上腺素>丙卡特罗>TRK-380>沙丁胺醇>BRL 37344。此外,异丙肾上腺素、丙卡特罗和 TRK-380 显著降低电刺激诱导收缩的幅度,抑制作用的顺序为异丙肾上腺素>丙卡特罗>TRK-380。

结论

人输尿管的松弛是由β(2)-和β(3)-肾上腺素能受体刺激介导的。β(3)-肾上腺素能受体激动剂具有松弛人输尿管的潜力,预计其在治疗输尿管结石方面的临床应用。

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