卡泊芬能减轻免疫缺陷 NSG 小鼠足底切口术后的机械和热超敏反应。

Comparative medicine Pub Date : 2024-04-01 Epub Date: 2024-03-29 DOI:10.30802/AALAS-CM-23-000058
Eden D Alamaw, Kerriann M Casey, Krystal Tien, Benjamin D Franco, Gregory Gorman, Renee M Cotton, Claude Nagamine, Katechan Jampachaisri, Patrick Sharp, Cholawat Pacharinsak, Monika K Huss
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引用次数: 0

摘要

据报道,免疫缺陷NSG小鼠对丁丙诺啡镇痛的反应较弱。在此,我们使用 NSG 小鼠比较了常用剂量的卡泊芬净(5 毫克/千克)与 5 倍和 10 倍剂量的卡泊芬净(25 毫克/千克和 50 毫克/千克)对减轻切口疼痛模型术后机械和热超敏反应的疗效。雄性和雌性 NSG 小鼠(n = 45)被随机分配到 4 组中的一组,在 3 天内每天接受皮下注射:生理盐水(5 mL/kg)、5 mg/kg 卡洛芬(Carp5)、25 mg/kg 卡洛芬(Carp25)和 50 mg/kg 卡洛芬(Carp50)。在手术前 24 小时以及手术后 4、24 和 48 小时对机械和热过敏性进行评估。在第一、第二和第三剂量后的第 0 天(2、4、12 和 23 小时)、第 1 天和第 2 天,分别测量另一组小鼠(n = 56)的血浆卡洛芬浓度。毒性通过每日粪便隐血检测(n = 27)以及大体和组织病理学评估(n = 15)进行评估。我们的结果表明,生理盐水组在整个研究过程中都表现出机械和热过敏。鲤鱼 5 在任何时间点都不会减轻机械或热过敏反应。鲤鱼 25 可减轻机械和热过敏(4 小时时间点除外)。一些经 Carp50 处理的小鼠出现了组织病理学异常(胃溃疡、溃疡性肠炎和肾脏病变)。血浆中的卡洛芬浓度与剂量和时间有关。我们的研究结果表明,在切口疼痛的 NSG 小鼠中,Carp25 比 Carp5 或 Carp50 能更有效地减轻术后机械和热超敏反应。因此,我们建议在使用免疫缺陷的 NSG 小鼠进行切口疼痛手术时提供 25 mg/kg SID 的卡泊芬钠。
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Carprofen Attenuates Postoperative Mechanical and Thermal Hypersensitivity after Plantar Incision in Immunodeficient NSG Mice.

Immunodeficient NSG mice are reported to be less responsive to buprenorphine analgesia. Here, we used NSG mice to compare the efficacy of the commonly used dose of carprofen (5 mg/kg) with 5 and 10 times that dose (25 and 50 mg/kg) for attenuating postoperative mechanical and thermal hypersensitivity following an incisional pain model. Male and female NSG mice (n = 45) were randomly assigned to one of 4 groups and received daily subcutaneous injections for 3 d: saline (5 mL/kg), 5 mg/kg carprofen (Carp5), 25 mg/kg carprofen (Carp25), and 50 mg/kg carprofen (Carp50). Mechanical and thermal hypersensitivity were assessed 24 h before and at 4, 24, and 48 h after surgery. Plasma carprofen concentrations were measured in a separate group of mice (n = 56) on days 0 (at 2, 4, 12, and 23 h), 1, and 2 after the first, second, and third doses, respectively. Toxicity was assessed through daily fecal occult blood testing (n = 27) as well as gross and histopathologic evaluation (n = 15). Our results indicated that the saline group showed both mechanical and thermal hypersensitivity throughout the study. Carp5 did not attenuate mechanical or thermal hypersensitivity at any time point. Carp25 attenuated mechanical and thermal (except for the 4-h time point) hypersensitivity. Carp50 attenuated only thermal hypersensitivity at 24 h. Fecal occult blood was detected in 1 of 8 Carp25-treated mice at 48 and 72 h. Histopathologic abnormalities (gastric ulceration, ulcerative enteritis, and renal lesions) were observed in some Carp50-treated mice. Plasma carprofen concentrations were dose and time dependent. Our results indicate that Carp25 attenuated postoperative mechanical and thermal hypersensitivity more effectively than Carp5 or Carp50 in NSG mice with incisional pain. Therefore, we recommend providing carprofen at 25 mg/kg SID for incisional pain procedures using immunodeficient NSG mouse.

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