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前列腺素E₂介导兔逼尿肌的自发性节律性收缩。

Prostaglandin E₂mediates spontaneous rhythmic contraction in rabbit detrusor muscle.

作者信息

Klausner Adam P, Johnson Corey M, Stike Aaron B, Speich John E, Sabarwal Vikram, Miner Amy S, Cleary MaryEllen, Koo Harry P, Ratz Paul H

机构信息

Department of Surgery/Division of Urology, Virginia Commonwealth University, Richmond, VA 23298-0118, USA.

出版信息

Can J Urol. 2011 Apr;18(2):5608-14.

Abstract

INTRODUCTION

The purpose of this investigation was to determine if prostaglandin E₂(PGE₂) is produced by rabbit detrusor free of urothelium and demonstrate that PGE₂ is responsible for the generation of spontaneous rhythmic contraction (SRC).

METHODS

A bioassay was performed in which contraction frequency in strips of rabbit detrusor was compared before and after addition of superfusate from incubating sections of rabbit detrusor. Specificity was determined by testing the effects of SC-51089, a PGE₂(EP1) antagonist. Effects on development of tension were determined in artery segments after treatment with increasing doses of PGE₂, PGF₂α, and TXA₂, and a section of femoral artery was used as a negative control. Confirmation of PGE2 production was then determined using EIA kits.

RESULTS

Increased rhythmic frequency was identified after superfusate from a section of rabbit detrusor free of urothelium was added to strips of detrusor from the same animal. Additional experiments demonstrated that rhythmic frequency generated after treatment with PGE₂ was significantly reduced after treatment with SC-51089. In artery smooth muscle, prostaglandin dose response experiments demonstrated that only TXA₂ induced contraction at physiologic doses (<10⁻⁷M). As a negative control, subsequent treatment of a section of femoral artery with detrusor superfusate failed to increase tension, confirming a lack of TXA₂ production. EIA confirmed that PGE₂ production increased by 4.8-fold in strips of detrusor free of urothelium after 15 minutes of incubation and that this production was blocked by ibuprofen and a COX-1 inhibitor.

CONCLUSIONS

Rabbit detrusor produces PGE₂ which is the most likely mediator of SRC.

摘要

引言

本研究的目的是确定前列腺素E₂(PGE₂)是否由无尿路上皮的兔逼尿肌产生,并证明PGE₂是自发性节律性收缩(SRC)产生的原因。

方法

进行了一项生物测定,比较了添加来自兔逼尿肌孵育切片的超滤液前后兔逼尿肌条的收缩频率。通过测试PGE₂(EP1)拮抗剂SC-51089的作用来确定特异性。在用递增剂量的PGE₂、PGF₂α和TXA₂处理后,测定对动脉段张力发展的影响,并将一段股动脉用作阴性对照。然后使用酶免疫分析试剂盒确定PGE₂产生的确认情况。

结果

将来自无尿路上皮的兔逼尿肌切片的超滤液添加到同一只动物的逼尿肌条中后,节律频率增加。进一步的实验表明,用SC-51089处理后,用PGE₂处理后产生的节律频率显著降低。在动脉平滑肌中,前列腺素剂量反应实验表明,只有TXA₂在生理剂量(<10⁻⁷M)下诱导收缩。作为阴性对照,随后用逼尿肌超滤液处理一段股动脉未能增加张力,证实缺乏TXA₂的产生。酶免疫分析证实,孵育15分钟后,无尿路上皮的逼尿肌条中PGE₂的产生增加了4.8倍,并且这种产生被布洛芬和一种COX-1抑制剂阻断。

结论

兔逼尿肌产生PGE₂,PGE₂最有可能是SRC的介质。

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