Effects of flunixin meglumine on the recovery of ischaemic equine colonic mucosa in vitro.

A J Morton, A Grosche, S A Matyjaszek, M M R Polyak, D E Freeman
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引用次数: 10

Abstract

Reasons for performing study: The effects of prostaglandins and nonsteroidal anti-inflammatory drugs (NSAIDs) on repair of equine intestinal mucosa are important since most horses with gastrointestinal diseases are routinely treated with NSAIDs, such as flunixin meglumine (FM), and these drugs can be toxic to equine gastrointestinal mucosa.

Hypothesis: Flunixin meglumine would not affect recovery of equine colonic mucosa in vitro, 18 h after a reversible ischaemic injury.

Methods: In 14 anaesthetised horses, a segment of pelvic flexure was subjected to 2 h of ischaemia and the horses were allowed to recover for 18 h. Seven horses received normal saline and 7 received FM, 1.1 mg/kg bwt i.v., at the end of ischaemia and 12 h later. Colonic mucosa was harvested during a second anaesthesia, 18 h after recovery from ischaemia and then horses were subjected to euthanasia. Transepithelial electrical resistance (TER) and transepithelial flux of tritiated mannitol were used to measure mucosal permeability during 4 h of incubation in Ussing chambers, with the following in vitro treatments: 1) no addition, 2) FM 14 µmol/l as powder, 3) FM 14 µmol/l in injectable form and 4) diluent for injectable FM. Histomorphological changes were assessed by light microscopy.

Results: There were no significant differences in any of the measurements between saline and FM treated horses. The mucosal height of the ischaemic FM tissues incubated in diluent was significantly decreased compared to the nonischaemic tissues.

Conclusions: Flunixin meglumine did not adversely affect barrier integrity in ischaemic equine colonic mucosa.

氟尼新大聚胺对马结肠缺血粘膜体外恢复的影响。
研究原因:前列腺素和非甾体抗炎药(NSAIDs)对马肠粘膜修复的作用是重要的,因为大多数患有胃肠道疾病的马常规使用非甾体抗炎药,如氟尼辛大明(FM),这些药物可能对马胃肠道粘膜有毒性。假设:氟尼新甲氨明不影响可逆缺血损伤后18小时体外马结肠黏膜的恢复。方法:14匹麻醉马,局部局部缺血2 h后恢复18 h,缺血结束后和12 h分别给予生理盐水7匹和FM 1.1 mg/kg bwt静脉注射。在缺血恢复后18小时的第二次麻醉中收集结肠黏膜,然后对马进行安乐死。用氚化甘露醇的经皮电阻(TER)和经皮通量测定在Ussing室培养4 h时的粘膜通透性,体外处理为:1)不添加,2)fm14µmol/l粉末,3)fm14µmol/l注射,4)fm14µmol/l注射稀释剂。光镜下观察组织形态学变化。结果:在生理盐水和FM治疗的马之间,任何测量都没有显着差异。与未缺血组织相比,用稀释液孵育的FM缺血组织的粘膜高度明显降低。结论:氟尼欣对缺血马结肠粘膜屏障完整性无不良影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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