Pharmacokinetics of Extended-Release Meloxicam in Tufted Titmice (Baeolophus bicolor) Following Subcutaneous Administration.

Brenton Mays, Emily Zhang, Elizabeth Buckles, Rebecca Tierce, Keely-Nicole Wharton
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Abstract

Analgesic regimens for laboratory-housed avian species remain poorly defined, with limited pharmacokinetic data available, particularly in passerine birds. This study characterized the pharmacokinetics of extended-release (ER) meloxicam in tufted titmice (Baeolophus bicolor) following single subcutaneous dosages of 3 and 6 mg/kg. We hypothesized ER meloxicam would sustain therapeutic plasma concentrations (>3,500 ng/mL), previously established in zebra finches and larger avian species, for 72 hours. Pharmacokinetic analysis revealed significantly higher Cmax and faster clearance at 6 mg/kg compared with 3 mg/kg. Although therapeutic plasma levels (>3,500 ng/mL) were observed at 1 hour postadministration, concentrations decreased below previously established therapeutic thresholds by 4 hours postinjection at both dosages. Histopathologic examination revealed no significant drug-related adverse effects. These findings suggest subcutaneous administration of ER meloxicam at 3 and 6 mg/kg does not sufficiently prolong therapeutic analgesia in tufted titmice, with a shorter therapeutic duration of action than previous findings with intramuscular meloxicam in small passerines.

缓释美洛昔康在山雀皮下给药的药动学研究。
实验室饲养的鸟类的镇痛方案仍然不明确,可获得的药代动力学数据有限,特别是雀形目鸟类。本研究以3和6 mg/kg的单次皮下剂量对美洛昔康在簇山雀体内的药代动力学进行了表征。我们假设ER meloxicam可以维持治疗血浆浓度(> 3500 ng/mL) 72小时,之前在斑胸草雀和大型鸟类中建立。药代动力学分析显示,与3mg /kg相比,6mg /kg的Cmax和清除率明显更高。虽然在给药后1小时观察到治疗血浆水平(> 3500 ng/mL),但在注射后4小时,两种剂量的浓度均降至先前设定的治疗阈值以下。组织病理学检查未发现明显的药物相关不良反应。这些发现表明,皮下给药3和6mg /kg的ER美洛昔康不能充分延长簇状山雀的治疗性镇痛,其作用时间比先前在小雀鸟中肌注美洛昔康的治疗时间短。
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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