Assessment of the Safety and Efficacy of Pre-emptive Use of Extended-release Buprenorphine for Mouse Laparotomy.

IF 1.2 3区 农林科学 Q3 VETERINARY SCIENCES
Goldia Chan, Catherine Si, M Russell Nichols, Lucy Kennedy
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引用次数: 2

Abstract

Buprenorphine is commonly used to control postoperative pain in rodents. Short-acting formulations of buprenorphine (bup-HCl) require frequent handling and restraint of animals for appropriate dosing, which can be stressful and confound research outcomes. Ethiqa XR (bup-ER) is an FDA-indexed extended-release buprenorphine formulation that is an alternative to bup-HCl in mice and rats. In the current study, we first evaluated the pharmacokinetics of bup-ER in male C57BL/6J mice by sampling blood at 10 time points, ranging from 30 min to 72 h after administration (n = 3 mice per time point). Average plasma concentrations fell below therapeutic levels at 48 h after administration. We also evaluated the safety of bup-ER when administered prior to surgery in combination with common anesthetics and the efficacy of bup-ER in mouse laparotomy. Anesthetic safety was studied by measuring respiratory rate, rectal temperature, and recovery time in groups of mice (n = 8) given bup-HCl, bup-ER, or saline in combination with isoflurane or ketamine-xylazine anesthesia. No differences were seen between analgesic treatment groups with either of the general anesthetics. To evaluate efficacy, mice (n = 10) were randomly allocated to receive either bup-ER (3.25 mg/kg) once presurgically, bup-HCl (0.1 mg/kg) presurgically and then every 8 h, or saline once before surgery. Mice underwent a sham laparotomy and were assessed for pain based on changes in weight, cageside ethogram, nesting consolidation test, rearing frequency, and nociception to von Frey testing at 6, 12, 24, 48, and 72 h after surgery. Cageside ethogram, rearing frequency, and von Frey testing showed significant differences between bup-ER-treated mice and saline controls in the early postoperative period. No significant effects between treatment groups were seen in daily weights or nesting consolidation scores. This study demonstrates that bup-ER can be safely administered before surgery and provides analgesia for up to 48 h after administration based on pharmacokinetic and behavioral data.

Abstract Image

Abstract Image

缓释丁丙诺啡用于小鼠剖腹手术的安全性和有效性评价。
丁丙诺啡常用于控制啮齿类动物术后疼痛。丁丙诺啡(bup-HCl)的短效制剂需要经常处理和约束动物以获得适当的剂量,这可能会造成压力并混淆研究结果。Ethiqa XR (bup-ER)是一种fda索引的缓释丁丙诺啡制剂,是小鼠和大鼠bup-HCl的替代品。在本研究中,我们首先通过在给药后30分钟至72小时的10个时间点(每个时间点n = 3只小鼠)采血来评估雄性C57BL/6J小鼠的bup-ER的药代动力学。平均血浆浓度在给药后48小时降至治疗水平以下。我们还评估了手术前与普通麻醉药联合使用bup-ER的安全性以及bup-ER在小鼠剖腹手术中的疗效。通过测量呼吸频率、直肠温度和恢复时间,研究各组小鼠(n = 8)分别给予bup-HCl、bup-ER或生理盐水联合异氟醚或氯胺酮-噻嗪麻醉的安全性。两种全麻的镇痛治疗组间无差异。为了评估疗效,将10只小鼠随机分配术前1次接受补强er (3.25 mg/kg),术前每8 h接受补强盐酸(0.1 mg/kg),术前1次接受生理盐水。在手术后6、12、24、48和72小时,对小鼠进行假剖腹手术,并根据体重变化、笼侧心电图、窝窝巩固试验、饲养频率和von Frey伤害感受试验来评估疼痛。在术后早期,bup- er处理小鼠与生理盐水对照组的笼侧心电图、饲养频率和von Frey测试显示有显著差异。治疗组之间的日体重或巢窝巩固评分没有显著影响。这项研究表明,基于药代动力学和行为数据,bup-ER可以在手术前安全给药,并在给药后48小时内提供镇痛。
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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来源期刊
CiteScore
3.10
自引率
35.30%
发文量
122
审稿时长
6-12 weeks
期刊介绍: The Journal of the American Association for Laboratory Animal Science (JAALAS) serves as an official communication vehicle for the American Association for Laboratory Animal Science (AALAS). The journal includes a section of refereed articles and a section of AALAS association news. All signed articles, including refereed articles and book reviews, editorials, committee reports, and news and commentary, reflect the individual views of the authors and are not official views of AALAS. The mission of the refereed section of the journal is to disseminate high-quality, peer-reviewed information on animal biology, technology, facility operations, management, and compliance as relevant to the AALAS membership. JAALAS accepts research reports (data-based) or scholarly reports (literature-based), with the caveat that all articles, including solicited manuscripts, must include appropriate references and must undergo peer review.
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