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阿洛司琼、西拉司琼和替加色罗可改变大鼠肠系膜血流,但不改变结肠血流。

Alosetron, cilansetron and tegaserod modify mesenteric but not colonic blood flow in rats.

机构信息

Research Unit of Translational Neurogastroenterology, Institute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria.

出版信息

Br J Pharmacol. 2009 Nov;158(5):1210-26. doi: 10.1111/j.1476-5381.2009.00392.x. Epub 2009 Sep 25.

Abstract

BACKGROUND AND PURPOSE

As the use of the 5-HT(3) receptor antagonist alosetron (GlaxoSmithKline) and the 5-HT(4) receptor agonist tegaserod (Novartis) in patients with irritable bowel syndrome has been associated with cases of ischaemic colitis, the effects of alosetron, cilansetron (Solvay) and tegaserod on the rat splanchnic circulation were evaluated.

EXPERIMENTAL APPROACH

Phenobarbital-anaesthetised rats were instrumented to record blood flow in the superior mesenteric artery and transverse colon and to calculate mesenteric and colonic vascular conductance.

KEY RESULTS

Intravenous alosetron (0.03-0.3 mg.kg(-1)) did not alter blood pressure or heart rate but reduced mesenteric blood flow and vascular conductance by 15-20%. This activity profile was also seen after intraduodenal alosetron and shared by the 5-HT(3) receptor antagonist cilansetron. In contrast, blood flow, vascular conductance and intraluminal pressure in the colon were not modified by alosetron and cilansetron. Intravenous or intraduodenal tegaserod (0.3-1.0 mg.kg(-1)) had no inhibitory effect on mesenteric and colonic blood flow. Peroral treatment of rats with alosetron or tegaserod for 7 days did not modify mesenteric haemodynamics at baseline and after blockade of nitric oxide synthesis. Mild inflammation induced by dextran sulphate sodium failed to provoke a vasoconstrictor effect of cilansetron in the colon.

CONCLUSIONS AND IMPLICATIONS

Alosetron and cilansetron, not tegaserod, caused a small and transient constriction of the rat mesenteric vascular bed, whereas blood flow in the colon remained unaltered. The relevance of these findings to the treatment-associated occurrence of ischaemic colitis in patients with irritable bowel syndrome remains open.

摘要

背景与目的

由于使用 5-HT(3)受体拮抗剂阿洛司琼(葛兰素史克)和 5-HT(4)受体激动剂替加色罗(诺华)治疗肠易激综合征患者与缺血性结肠炎有关,因此评估了阿洛司琼、西拉司琼(索法雷尔)和替加色罗对大鼠内脏循环的影响。

实验方法

用苯巴比妥麻醉大鼠,记录肠系膜上动脉和横结肠的血流量,并计算肠系膜和结肠血管的传导能力。

主要结果

静脉注射阿洛司琼(0.03-0.3mg/kg)不改变血压或心率,但使肠系膜血流量和血管传导能力降低 15-20%。这种活性谱也见于十二指肠内给予阿洛司琼,与 5-HT(3)受体拮抗剂西拉司琼共享。相比之下,阿洛司琼和西拉司琼对结肠的血流量、血管传导能力和腔内压力没有影响。静脉内或十二指肠内给予替加色罗(0.3-1.0mg/kg)对肠系膜和结肠的血流没有抑制作用。大鼠口服阿洛司琼或替加色罗治疗 7 天,在一氧化氮合成阻断后,对基础和基础状态下的肠系膜血液动力学没有改变。葡聚糖硫酸钠引起的轻度炎症未能引起西拉司琼在结肠中的血管收缩作用。

结论和意义

阿洛司琼和西拉司琼而非替加色罗引起大鼠肠系膜血管床短暂的小收缩,而结肠的血流仍未改变。这些发现与肠易激综合征患者治疗相关的缺血性结肠炎的发生有关,仍有待进一步研究。

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Is irritable bowel syndrome an inflammatory disorder?肠易激综合征是一种炎症性疾病吗?
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Guide to Receptors and Channels (GRAC), 3rd edition.《受体与通道指南》(GRAC),第三版。
Br J Pharmacol. 2008 Mar;153 Suppl 2(Suppl 2):S1-209. doi: 10.1038/sj.bjp.0707746.
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Assessment of potential risk factors associated with ischaemic colitis.与缺血性结肠炎相关的潜在风险因素评估。
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