The effect of glycopyrrolate on heart rate and intestinal motility in conscious horses

S. Singh , W. McDonell , S. Young , D. Dyson
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引用次数: 24

Abstract

Glycopyrrolate (GLY) is a synthetic quaternary ammonium anticholinergic compound which offers a number of advantages over atropine, including less arrhythmogenic influence and lack of significant effect upon the central nervous system, eyes and foetus. Five healthy horses (7.4 ± 2.2 years, 462 ± 31.7 kg) were administered 2.5, 5 and 10 μg/kg doses of GLY iv in a randomised and blinded manner with at least 48 h between treatments. The electrocardiogram and heart rate were recorded on an oscilloscopic and chart recorder while gastrointestinal (GIT) motility was assessed by auscultation of 4 abdominal quadrants, assigning a subjective score from 0 (no motility) to 4 (normal motility). Heart rate, which was observed at baseline, 2, 5, 10, 15, 30 min, and 1, 2, 3, 4, 6, 9, 12, 18 and 24 h post GLY, revealed no change with the 2.5 μg/kg dose, and an increase with 5 μg/kg (59%) and 10 μg/kg (109%) for up to 1 h. The 2.5 and 5 μg/kg doses did not prevent the development of second degree atrioventricular block in some horses for up to 15 min, while the 10 μg/kg dose eliminated any pre-existing block within 5 min. There was a complete loss of GIT motility with the 5 and 10 μg/kg doses and partial loss with the 2.5 μg/kg dose. Subsequent return of motility was apparently dose-dependent with 50% of baseline motility score returning in 2.4, 6.4 and 11.5 h with 2.5, 5 and 10 μg/kg doses, respectively. Two horses receiving a 10 μg/kg dose developed abdominal discomfort. Passage of faeces and appetite were not significantly different with any dose. Glycopyrrolate did not induce any change in the pupillary response to a light source at any stage of observation. The results of this study indicate that 5 μg/kg induces a reasonable increase in heart rate without affecting GIT motility for an excessive length of time in awake, healthy, adult, unsedated horses.

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格隆吡咯烷酸酯对清醒马心率和肠道运动的影响
吡咯烷酸酯(GLY)是一种合成的季铵抗胆碱能化合物,与阿托品相比具有许多优点,包括对心律失常的影响较小,对中枢神经系统、眼睛和胎儿没有显著影响。五匹健康马(7.4±2.2岁,462±31.7 kg)以随机和盲法分别静脉注射2.5、5和10μg/kg剂量的GLY,两次治疗间隔至少48小时。心电图和心率记录在示波器和图表记录器上,胃肠道(GIT)运动通过4个腹部象限的听诊进行评估,主观评分从0(无运动)到4(运动正常)。在基线、GLY后2、5、10、15、30分钟以及1、2、3、4、6、9、12、18和24小时观察到的心率显示,2.5μg/kg剂量没有变化,5μg/kg(59%)和10μg/kg(109%)剂量增加1小时。2.5和5μg/kg剂量在长达15分钟的时间内没有阻止某些马出现二度房室传导阻滞,而10μg/kg剂量在5分钟内消除了任何预先存在的阻滞。5μg/kg和10μg/kg的剂量完全丧失了GIT的运动能力,2.5μg/kg剂量则部分丧失。随后的运动恢复明显呈剂量依赖性,2.5、5和10μg/kg剂量分别在2.4、6.4和11.5小时内恢复50%的基线运动评分。接受10μg/kg剂量的两匹马出现腹部不适。粪便的排泄和食欲在任何剂量下都没有显著差异。在任何观察阶段,吡咯烷酸酯都不会引起瞳孔对光源的反应发生任何变化。这项研究的结果表明,在清醒、健康、成年、未交配的马中,5μg/kg可诱导心率合理增加,而不会在过长时间内影响GIT运动。
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