Postoperative Analgesia Due to Sustained-Release Buprenorphine, Sustained-Release Meloxicam, and Carprofen Gel in a Model of Incisional Pain in Rats (Rattus norvegicus)

被引:0
|
作者
Seymour, Travis L. [1 ]
Adams, Sean C. [1 ]
Felt, Stephen A. [1 ]
Jampachaisri, Katechan [3 ]
Yeomans, David C. [2 ]
Pacharinsak, Cholawat [1 ]
机构
[1] Stanford Univ, Dept Comparat Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Anesthesia, Stanford, CA 94305 USA
[3] Naresuan Univ, Dept Math, Phitsanulok, Thailand
来源
JOURNAL OF THE AMERICAN ASSOCIATION FOR LABORATORY ANIMAL SCIENCE | 2016年 / 55卷 / 03期
关键词
DRINKING-WATER; PHARMACOKINETICS; DURATION; ACETAMINOPHEN; INHIBITION; TRAMADOL; RABBITS; PATCHES;
D O I
暂无
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Postoperative analgesia in laboratory rats is complicated by the frequent handling associated with common analgesic dosing requirements. Here, we evaluated sustained-release buprenorphine (Bup-SR), sustained-release meloxicam (Melox-SR), and carprofen gel (CG) as refinements for postoperative analgesia. The aim of this study was to investigate whether postoperative administration of Bup-SR, Melox-SR, or CG effectively controls behavioral mechanical and thermal hypersensitivity in a rat model of incisional pain. Rats were randomly assigned to 1 of 5 treatment groups: saline, 1 mL/kg SC BID; buprenorphine HCl (Bup HCl), 0.05 mg/kg SC BID; Bup-SR, 1.2 mg/kg SC once; Melox-SR, 4 mg/kg SC once; and CG, 2 oz PO daily. Mechanical and thermal hypersensitivity were tested daily from day-1 through 4. Bup HCl and Bup-SR attenuated mechanical and thermal hypersensitivity on days 1 through 4. Melox-SR and CG attenuated mechanical hypersensitivity but not thermal hypersensitivity on days 1 through 4. Plasma concentrations, measured by using UPLC with mass spectrometry, were consistent between both buprenorphine formulations. Gross pathologic examination revealed no signs of toxicity in any group. These findings suggest that postoperative administration of Bup HCl and Bup-SR-but not Melox-SR or CG-effectively attenuates mechanical and thermal hypersensitivity in a rat model of incisional pain.
引用
收藏
页码:300 / 305
页数:6
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