Population pharmacokinetics of a single oral dose of gabapentin identifies rapid plasma clearance in rehabilitated Pacific harbor seal pups (Phoca vitulina richardii).

IF 1.4 3区 农林科学 Q2 VETERINARY SCIENCES
Tess A Rooney, Heather Knych, Mattison Peters, Jenessa Gjeltema, Cara Field
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Abstract

Objective: Determine the pharmacokinetic parameters of a single dose of gabapentin administered orally in healthy weaned Pacific harbor seal (HS) pups (Phoca vitulina richardii).

Methods: In the spring of 2023, rehabilitated HS pups were enrolled in this pharmacokinetic study. Seals were administered 10 mg/kg of gabapentin orally in a fish. A sparse sampling model was employed to collect blood samples from 0.25 to 48 hours after drug administration. Plasma drug concentrations were determined using liquid chromatography-tandem mass spectrometry. Pharmacokinetic parameters were determined using noncompartmental analysis for sparse data.

Results: 15 HSs were included in this study. The mean peak plasma concentration was 7,669.4 ng/mL, the mean time to peak plasma concentration was 1 hour, the mean area under the concentration-versus-time curve from time 0 to infinity was 23,811.8 h·ng/mL, and the mean terminal half-life was 1.9 hours. No adverse effects were observed in any HSs.

Conclusions: The plasma concentration of gabapentin that confers analgesia is not known in veterinary species. During this study, mean gabapentin concentrations exceeded the concentration estimated to treat neuropathic pain in humans only at 1 hour.

Clinical relevance: Gabapentin was rapidly absorbed and eliminated in HSs, indicating that higher dosages and/or frequent dosing of gabapentin may be needed to maintain targeted plasma concentrations in young HSs. Additional studies to investigate the clinical efficacy of gabapentin in veterinary species are warranted, and clinical discretion should be used when applying these results to patients outside of the specific demographic group studied here.

单次口服加巴喷丁的群体药代动力学鉴定康复的太平洋斑海豹幼崽(Phoca vitulina richardii)的快速血浆清除。
目的:测定单剂量加巴喷丁在健康断奶太平洋斑海豹(phca vitulina richardii)仔体内的药动学参数。方法:于2023年春季选取康复的HS幼犬进行药代动力学研究。给海豹口服加巴喷丁10mg /kg给鱼。在给药后0.25 ~ 48小时采用稀疏抽样模型采集血样。采用液相色谱-串联质谱法测定血浆药物浓度。采用稀疏数据的非区隔分析确定药代动力学参数。结果:15例HSs纳入本研究。血药浓度平均峰值为7669.4 ng/mL,到达血药浓度峰值的平均时间为1 h,从时间0到无穷远的血药浓度-时间曲线下的平均面积为23811.8 h·ng/mL,平均终末半衰期为1.9 h。未观察到任何HSs的不良反应。结论:加巴喷丁给药的血药浓度在兽药中尚不清楚。在这项研究中,加巴喷丁的平均浓度仅在1小时内超过了治疗人类神经性疼痛的估计浓度。临床相关性:加巴喷丁在HSs中被迅速吸收和消除,表明可能需要更高剂量和/或频繁给药加巴喷丁来维持年轻HSs的靶血药浓度。进一步研究加巴喷丁在兽药中的临床疗效是有必要的,在将这些结果应用于本研究特定人口统计学群体之外的患者时,应酌情考虑临床。
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来源期刊
CiteScore
1.70
自引率
10.00%
发文量
186
审稿时长
3 months
期刊介绍: The American Journal of Veterinary Research supports the collaborative exchange of information between researchers and clinicians by publishing novel research findings that bridge the gulf between basic research and clinical practice or that help to translate laboratory research and preclinical studies to the development of clinical trials and clinical practice. The journal welcomes submission of high-quality original studies and review articles in a wide range of scientific fields, including anatomy, anesthesiology, animal welfare, behavior, epidemiology, genetics, heredity, infectious disease, molecular biology, oncology, pharmacology, pathogenic mechanisms, physiology, surgery, theriogenology, toxicology, and vaccinology. Species of interest include production animals, companion animals, equids, exotic animals, birds, reptiles, and wild and marine animals. Reports of laboratory animal studies and studies involving the use of animals as experimental models of human diseases are considered only when the study results are of demonstrable benefit to the species used in the research or to another species of veterinary interest. Other fields of interest or animals species are not necessarily excluded from consideration, but such reports must focus on novel research findings. Submitted papers must make an original and substantial contribution to the veterinary medicine knowledge base; preliminary studies are not appropriate.
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