首页> 美国卫生研究院文献>Journal of the American Association for Laboratory Animal Science : JAALAS >Effects of Buprenorphine Methylnaltrexone and Their Combination on Gastrointestinal Transit in Healthy New Zealand White Rabbits
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Effects of Buprenorphine Methylnaltrexone and Their Combination on Gastrointestinal Transit in Healthy New Zealand White Rabbits

机译:丁丙诺啡甲基纳曲酮及其组合对健康新西兰白兔胃肠道转运的影响

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摘要

Among the many analgesic agents available, buprenorphine appears to be the analgesic used most often in rabbits. Unfortunately, deleterious side effects of opioids, such as gastrointestinal stasis and anorexia, may discourage the use of these agents. Methylnaltrexone is a peripheral opioid antagonist that ameliorates opioid-induced gastrointestinal stasis in others species yet preserves the analgesic effects of buprenorphine. We evaluated whether methylnaltrexone reversed buprenorphine-induced gastrointestinal stasis in 8 healthy male New Zealand White rabbits. To measure gastrointestinal transit time, each rabbit received 20 barium-filled spheres through an orogastric tube. Rabbits then received 4 treatments in random order: buprenorphine (0.05 mg/kg SC), methylnaltrexone (1 mg/kg SC), both agents combined (B+M), or normal saline (control) every 12 h for 2 d. Fecal production was measured every 6 h, and water and food consumption, and body weight, were measured daily, for 5 d after each treatment. The time to appearance of the first sphere was significantly longer for buprenorphine group than for control and methylnaltrexone groups. Daily fecal output was lowest for buprenorphine and B+M, intermediate for control, and highest for methylnaltrexone. Water and food consumption were lower for groups buprenorphine and B+M than for control and methylnaltrexone. Body weight was not affected. In conclusion, treatment with buprenorphine 0.05 mg/kg BID for 2 d in healthy rabbits decreased food and water consumption, prolonged gastrointestinal transit time and decreased the fecal output. Coadministration of methylnaltrexone at 1 mg/kg did not alleviate these negative side effects.
机译:在许多可用的止痛剂中,丁丙诺啡似乎是家兔中最常用的止痛剂。不幸的是,阿片类药物的有害副作用,例如胃肠道淤滞和厌食,可能会阻止这些药物的使用。甲基纳曲酮是一种外周阿片类拮抗剂,可减轻其他物种中阿片类药物引起的胃肠道淤积,同时保留丁丙诺啡的镇痛作用。我们评估了甲基纳曲酮是否在8只健康的雄性新西兰白兔中逆转了丁丙诺啡引起的胃肠道淤积。为了测量胃肠道的通过时间,每只兔子通过口胃管接受20个充满钡的球。然后,兔子随机接受4种治疗:丁丙诺啡(0.05 mg / kg SC),甲基纳曲酮(1 mg / kg SC),两种药物合用(B + M)或生理盐水(对照)每12小时治疗2 d。每6小时测量一次粪便的产生,并在每次治疗后5天每天测量水和食物的消耗量以及体重。丁丙诺啡组第一个球出现的时间明显长于对照组和甲基纳曲酮组。丁丙诺啡和B + M的每日粪便产量最低,对照组为中间,甲基纳曲酮最高。丁丙诺啡和B + M组的水和食物消耗量低于对照组和甲基纳曲酮。体重不受影响。总之,在健康兔中用丁丙诺啡0.05 mg / kg BID治疗2 d可减少食物和水的消耗,延长胃肠道的通过时间并减少粪便的排出量。甲基纳曲酮1 mg / kg的共同给药不能缓解这些不良副作用。

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