口服米氮平在豚鼠体内的初步药代动力学及食欲刺激功效()

Preliminary Pharmacokinetics and Appetite Stimulant Efficacy of Oral Mirtazapine in Guinea Pigs ().

作者信息

Ayers Jessica, Stietzle Elizabeth, Ellis Megan, Kim Jeffrey, Kendall Lon V

机构信息

Laboratory Animal Resources Department, Colorado State University, Fort Collins, CO 80523, USA.

College of Veterinary Medicine, Kansas State University, Manhattan, KS 66502, USA.

出版信息

Animals (Basel). 2025 Jul 31;15(15):2256. doi: 10.3390/ani15152256.

Abstract

Guinea pigs used in research may experience inappetence or decreased intestinal motility, which can significantly compromise their welfare. This study evaluates the use of mirtazapine on appetite and intestinal motility in guinea pigs. An initial pharmacokinetics and efficacy study was performed using healthy male guinea pigs administered mirtazapine at 1.88, 3.75, or 7.5 mg orally once daily for four days ( = 6), in a crossover design where all animals received all doses. Body, feed, and fecal weights were taken daily for 4 days. There were no significant differences in weight gains, feed intake, or fecal output as compared to guinea pigs given saline only ( = 3). Blood was collected under anesthesia at 0, 0.5, 1, 2, 8, 12, and 24 h post-administration. Pharmacokinetic analysis completed after the first dose showed peak plasma levels at 30 min, then falling below the limit of detection between 8 h and 12 h at all doses. Based on the pharmacokinetic profile, a follow-up study was performed in another set of healthy male guinea pigs with every 8 h dosing at 1.88 mg orally for 5 days ( = 6). There was a significant increase in feed intake during mirtazapine administration as compared to baseline intake, but no significant difference in weight gains. This study shows that mirtazapine can be used as an appetite stimulant in guinea pigs but must be dosed at least every eight hours to be effective.

摘要

用于研究的豚鼠可能会出现食欲不振或肠道蠕动减弱的情况,这会严重损害它们的健康。本研究评估了米氮平对豚鼠食欲和肠道蠕动的作用。最初进行了一项药代动力学和疗效研究,使用健康雄性豚鼠,以交叉设计,所有动物接受所有剂量,每天口服一次米氮平,剂量分别为1.88、3.75或7.5毫克,持续四天(每组6只)。连续4天每天记录体重、进食量和粪便重量。与仅给予生理盐水的豚鼠相比(每组3只),体重增加、进食量或粪便排出量没有显著差异。给药后0、0.5、1、2、8、12和24小时在麻醉状态下采集血液。首剂给药后完成的药代动力学分析显示,所有剂量的血浆峰值水平均在30分钟出现,然后在8小时至12小时之间降至检测限以下。基于药代动力学特征,在另一组健康雄性豚鼠中进行了一项后续研究,每8小时口服1.88毫克,持续5天(每组6只)。与基线摄入量相比,米氮平给药期间进食量显著增加,但体重增加没有显著差异。本研究表明,米氮平可作为豚鼠的食欲刺激剂,但必须至少每8小时给药一次才有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38e9/12345486/b34f62e70003/animals-15-02256-g001.jpg

本文引用的文献

[9]
Prokinetic effects of mirtazapine on gastrointestinal transit.

Am J Physiol Gastrointest Liver Physiol. 2014-3-13

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