Pharmacokinetics of Trazodone in Hispaniolan Parrots (Amazona ventralis).

IF 0.6 4区 农林科学 Q3 VETERINARY SCIENCES Journal of Avian Medicine and Surgery Pub Date : 2024-07-01 DOI:10.1647/AVIANMS-D-23-00047
Haley M Straub, Thomas N Tully, Levent Dirikolu, Andreas F Lehner, Justin Zyskowski, John Buchweitz
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Abstract

The objective of this study was to establish the pharmacokinetics of a single oral dose of trazodone in the Hispaniolan Amazon parrot (Amazona ventralis). Trazodone is a selective serotonin antagonist and reuptake inhibitor used commonly in both human and veterinary medicine as an antidepressant behavioral modification medicine. A single oral dose of compounded trazodone hydrochloride solution (20 mg/mL) at 50 mg/kg was administered to a total of 7 healthy adult Hispaniolan Amazon parrots. The 7 healthy adult parrots ranged in age from 10 to 15 years and weighed 228 to 323g. Blood was collected at baseline (2 weeks before study) and at 1, 2, 4, 6, 10, and 14 hours post-drug administration. Plasma concentrations of both trazodone and its active metabolite m-chlorophenylpiperazine (mCPP) were measured via liquid chromatography tandem mass spectrometry. Noncompartmental pharmacokinetic analysis was completed. The half-life (t1/2) ± SD of trazodone for the Hispaniolan parrots was 1.89 ± 0.49 hours, and the t1/2 ± SD of mCPP metabolite was 1.9 ± 0.55 hours. Maximum serum drug concentrations, or Cmax (ng/mL), were 738.3 ± 285.3 for trazodone. Times to achieve Cmax (hours) for trazadone and the mCPP metabolite were 1 hour and 2 hours postdosing, respectively. While this study did not establish the behavioral effects of trazodone, no adverse side effects were observed throughout the 48-hour period following drug administration and blood collection. Our results indicate that the oral administration of a 50-mg/kg single dose of trazodone to Hispaniolan parrots may be considered a safe dose. Plasma concentrations are comparable to previously published values in humans, dogs, horses, and pigeons (Columba livia domestica) for up to 14 hours following dosing. This study indicates that further studies are needed to establish the pharmacodynamics and the efficacy of trazodone in the medical management of behavioral problems in psittacine species.

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特拉唑酮在伊斯帕尼奥兰鹦鹉(Amazona ventralis)体内的药代动力学。
本研究旨在确定伊斯帕尼奥拉亚马逊鹦鹉(Amazona ventralis)单次口服曲唑酮的药代动力学。曲唑酮(Trazodone)是一种选择性血清素拮抗剂和再摄取抑制剂,常用于人类和兽医的抗抑郁行为矫正药物。给 7 只健康的成年伊斯帕尼奥拉亚马逊鹦鹉单次口服 50 毫克/千克的复方盐酸曲唑酮溶液(20 毫克/毫升)。这 7 只健康成年鹦鹉的年龄在 10 至 15 岁之间,体重在 228 至 323 克之间。在基线(研究前 2 周)和用药后 1、2、4、6、10 和 14 小时采集血液。血浆中曲唑酮及其活性代谢物间氯苯基哌嗪(mCPP)的浓度通过液相色谱串联质谱法进行测定。完成了非室药代动力学分析。在伊斯帕尼奥兰鹦鹉体内,曲唑酮的半衰期(t1/2)(± SD)为 1.89 ± 0.49 小时,mCPP 代谢物的半衰期(t1/2)(± SD)为 1.9 ± 0.55 小时。曲唑酮的最大血清药物浓度或Cmax(纳克/毫升)为738.3 ± 285.3。曲唑酮和mCPP代谢物达到Cmax的时间(小时)分别为用药后1小时和2小时。虽然这项研究没有确定曲唑酮的行为效应,但在用药和采血后的 48 小时内没有观察到任何不良副作用。我们的研究结果表明,为伊斯帕尼奥拉鹦鹉口服 50 毫克/千克的单剂量曲唑酮可被视为安全剂量。在服药后的 14 小时内,血浆浓度与之前公布的人类、狗、马和鸽子(Columba livia domestica)的血浆浓度值相当。这项研究表明,要确定曲唑酮在治疗鹦科动物行为问题方面的药效学和疗效,还需要进一步的研究。
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
Journal of Avian Medicine and Surgery
Journal of Avian Medicine and Surgery 农林科学-兽医学
CiteScore
0.90
自引率
0.00%
发文量
52
审稿时长
>36 weeks
期刊介绍: The Journal of Avian Medicine and Surgery is an international journal of the medicine and surgery of both captive and wild birds. Published materials include scientific articles, case reports, editorials, abstracts, new research, and book reviews.
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