Ting Allison Kah Yann, Tay Vanessa Shu Yu, Chng Hui Ting, Xie Shangzhe
National University of Singapore, Department of Pharmacy, 18 Science Drive 4 Blk S4A Level 3, Singapore, 117559.
Mandai Wildlife Group, 80 Mandai Lake Road, Singapore, 729826.
Vet Anim Sci. 2022 Aug 8;17:100267. doi: 10.1016/j.vas.2022.100267. eCollection 2022 Sep.
Non-steroidal anti-inflammatory drugs (NSAIDs) and opioids are analgesics used for moderate to severe pain in many animals, including reptiles. However, reptilian dosing regimens are often extrapolated from other animal species. This is not ideal as inter- and intra-species variability in physiology may result in varied drug disposition. Therefore, this critical review aims to collate data from pharmacological studies of selected NSAIDs and opioids performed in reptile and provide an analysis and discussion on the existing pharmacodynamic knowledge and pharmacokinetic data of NSAIDs and opioids use in reptiles. Additionally, key pharmacokinetic trends that may aid dosing of NSAIDs and opioids in reptiles will also be highlighted. Most of the existing reports of NSAID used in reptiles did not observe any adverse effects directly associated to the respective NSAID used, with meloxicam being the most well-studied. Despite the current absence of analgesic efficacy studies for NSAIDs in reptiles, most reports observed behavioural improvements in reptiles after NSAID treatment. Fentanyl and morphine were studied in the greatest number of reptile species with analgesic effects observed with the doses used, while adverse effects such as sedation were observed most with butorphanol use. While pharmacokinetic trends were drug- and species-specific, it was observed that clearance (CL) of drugs tended to be higher in squamates compared to chelonians. The half-life (t) of meloxicam also appeared to be longer when dosed orally compared to other routes of drug administration. This could have been due to absorption-rate limited disposition. Although current data provided beneficial information, there is an urgent need for future research on NSAID and opioid pharmacology to ensure the safe and effective use of opioids in reptiles.
非甾体抗炎药(NSAIDs)和阿片类药物是用于包括爬行动物在内的许多动物中度至重度疼痛的镇痛药。然而,爬行动物的给药方案通常是从其他动物物种推断而来的。这并不理想,因为种间和种内生理差异可能导致药物处置不同。因此,本综述旨在整理在爬行动物中进行的选定NSAIDs和阿片类药物的药理学研究数据,并对NSAIDs和阿片类药物在爬行动物中使用的现有药效学知识和药代动力学数据进行分析和讨论。此外,还将突出可能有助于爬行动物NSAIDs和阿片类药物给药的关键药代动力学趋势。大多数关于爬行动物使用NSAIDs的现有报告未观察到与所使用的相应NSAIDs直接相关的任何不良反应,其中美洛昔康是研究最多的。尽管目前缺乏NSAIDs在爬行动物中的镇痛效果研究,但大多数报告观察到NSAIDs治疗后爬行动物的行为有所改善。芬太尼和吗啡在最多的爬行动物物种中进行了研究,在所使用的剂量下观察到了镇痛效果,而布托啡诺使用时观察到的镇静等不良反应最多。虽然药代动力学趋势因药物和物种而异,但观察到有鳞目动物的药物清除率(CL)往往比龟鳖目动物更高。与其他给药途径相比,口服美洛昔康时其半衰期(t)似乎也更长。这可能是由于吸收速率限制的处置方式。尽管目前的数据提供了有益的信息,但迫切需要未来对NSAIDs和阿片类药物药理学进行研究,以确保阿片类药物在爬行动物中的安全有效使用。