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外周5-羟色胺1A受体在雌性大鼠膀胱出口部分梗阻相关逼尿肌过度活动中的作用

Role of peripheral 5-HT1A receptors in detrusor over activity associated with partial bladder outlet obstruction in female rats.

作者信息

Mittra Shivani, Malhotra Shivani, Naruganahalli Krishna S, Chugh Anita

机构信息

Department of Pharmacology, NDDR, Ranbaxy Research Laboratories, Plot No 20, Udyog Vihar Industrial Area, Sector 18, Gurgaon-122001, Haryana, India.

出版信息

Eur J Pharmacol. 2007 Apr 30;561(1-3):189-93. doi: 10.1016/j.ejphar.2007.01.031. Epub 2007 Feb 1.

Abstract

We have investigated the role of peripheral 5-hydroxytryptamine 1A (5-HT(1A)) receptors and their probable up-regulation in rat model of partial bladder outlet obstruction. Bladder outlet obstruction was induced in adult female rats, hypertropic bladders were harvested after 6 weeks and isometric contractions of bladder strips were recorded. A marked spontaneous activity of the bladder was observed in obstructed bladder strips compared to control strips. The effect of alpha(1A/1D)-adrenergic antagonist, tamsulosin, was observed to be inhibitory on the spontaneous contractions albeit at higher doses (10, 30 and 100 nM). As tamsulosin at higher doses also has high affinity for 5-HT(1A) receptors, the role of peripheral 5-HT(1A) receptors in overactive bladder was hypothesized. 8-hydroxy-2-(di-n-propylamino) tetralin [8-OH-DPAT], a selective 5-HT(1A) receptor agonist, dose-dependently induced significant contractions in the obstructed bladder strips, compared to control bladders. N-[2-[4-(2-methoxyphenyl) piperazin-1-yl]ethyl]-N-pyridin-2-yl-cyclohexanecarboxamide dihydrochloride (WAY-100635), a selective 5-HT(1A) receptor antagonist, competitively antagonized the contractile response to 8-OH-DPAT in obstructed bladder strips in a dose-dependent manner. Tamsulosin at a higher dose was also observed to antagonize the responses to 8-OH-DPAT. Taken together, these observations suggest the involvement of peripheral 5-HT(1A) receptors in detrusor over activity associated with bladder outlet obstruction in female rats.

摘要

我们研究了外周5-羟色胺1A(5-HT(1A))受体的作用及其在大鼠部分膀胱出口梗阻模型中可能的上调情况。对成年雌性大鼠诱导膀胱出口梗阻,6周后摘取肥厚的膀胱并记录膀胱条的等长收缩。与对照条相比,梗阻膀胱条中观察到膀胱有明显的自发活动。观察到α(1A/1D)-肾上腺素能拮抗剂坦索罗辛对自发收缩有抑制作用,尽管是在较高剂量(10、30和100 nM)时。由于高剂量的坦索罗辛对5-HT(1A)受体也有高亲和力,因此推测外周5-HT(1A)受体在膀胱过度活动中的作用。8-羟基-2-(二正丙基氨基)四氢萘[8-OH-DPAT],一种选择性5-HT(1A)受体激动剂,与对照膀胱相比,在梗阻膀胱条中剂量依赖性地诱导出显著收缩。N-[2-[4-(2-甲氧基苯基)哌嗪-1-基]乙基]-N-吡啶-2-基-环己烷甲酰胺二盐酸盐(WAY-100635),一种选择性5-HT(1A)受体拮抗剂,以剂量依赖性方式竞争性拮抗梗阻膀胱条中对8-OH-DPAT的收缩反应。还观察到高剂量的坦索罗辛也拮抗对8-OH-DPAT的反应。综上所述,这些观察结果表明外周5-HT(1A)受体参与了雌性大鼠膀胱出口梗阻相关的逼尿肌过度活动。

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