首页> 美国卫生研究院文献>Journal of the American Association for Laboratory Animal Science : JAALAS >Effects of Multimodal Analgesia with Low-Dose Buprenorphine and Meloxicam on Fecal Glucocorticoid Metabolites after Surgery in New Zealand White Rabbits (Oryctolagus cuniculus)
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Effects of Multimodal Analgesia with Low-Dose Buprenorphine and Meloxicam on Fecal Glucocorticoid Metabolites after Surgery in New Zealand White Rabbits (Oryctolagus cuniculus)

机译:小剂量丁丙诺啡和美洛昔康多模式镇痛对新西兰白兔手术后粪便糖皮质激素代谢产物的影响

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摘要

Despite the increasing use of rabbits as companion animals and models for biomedical research, rabbits have not been extensively studied to identify an efficacious postsurgical analgesic that does not cause systemic complications. The synergy of NSAID and systemic opioids is well-documented, and their combined use reduces the amount of either drug required for adequate analgesia. We measured fecal corticosterone metabolites (FCM) in rabbits after a minimally invasive vascular cut-down procedure. Rabbits received buprenorphine (0.03 mg/kg SC every 12 h for 3 d), meloxicam (0.2 mg/kg SC every 24 h for 3 d), buprenorphine–meloxicam (0.01 mg/kg–0.1 mg/kg SC every 24 h for 3 d), or a single dose of 0.5% bupivacaine (0.5 mL) infused locally at the incision site. By day 3 after surgery, buprenorphine, meloxicam, and bupivacaine groups showed elevated FCM levels, which continued to rise until day 7 and then gradually returned to baseline by day 28. In the buprenorphine–meloxicam group, FCM was relatively unchanged until day 3, when treatment was discontinued, and then began to rise. Rabbits in the buprenorphine–meloxicam group gained more weight over the 28-d study than did those in the other 3 treatment groups. This study shows that in rabbits low-dose buprenorphine administered with meloxicam effectively mitigates the FCM response that develops after surgery without the adverse effects associated with higher doses.
机译:尽管越来越多地将兔子用作生物医学研究的伴侣动物和模型,但尚未对兔子进行广泛的研究以鉴定不会引起全身并发症的有效的术后镇痛药。 NSAID和全身阿片类药物的协同作用已得到充分证明,并且它们的联合使用可减少充分镇痛所需的两种药物的量。在微创血管切开手术后,我们测量了兔子的粪便皮质酮代谢物(FCM)。兔子接受丁丙诺啡(0.03 mg / kg SC每12小时,持续3 d),美洛昔康(0.2 mg / kg SC每24 h,持续3 d),丁丙诺啡-美洛昔康(0.01 mg / kg–0.1 mg / kg SC每24小时) 3 d),或在切口部位局部注入0.5%布比卡因(0.5 mL)。手术后第3天,丁丙诺啡,美洛昔康和布比卡因组显示出较高的FCM水平,一直持续到第7天,然后在第28天逐渐回到基线。在丁丙诺啡-美洛昔康组中,直到第3天,FCM相对不变,当治疗中断后,又开始上升。在28天的研究中,丁丙诺啡-美洛昔康组的兔子比其他3个治疗组的兔子体重增加。这项研究表明,在兔子中服用美洛昔康的小剂量丁丙诺啡能有效缓解术后出现的FCM反应,而不会出现大剂量的不良反应。

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