Suppr超能文献

美洛昔康在成年山羊体内的药代动力学及其对去角幼羊的镇痛效果。

Pharmacokinetics of meloxicam in adult goats and its analgesic effect in disbudded kids.

作者信息

Ingvast-Larsson C, Högberg M, Mengistu U, Olsén L, Bondesson U, Olsson K

机构信息

Division of Pathology, Pharmacology and Toxicology, Department of Biomedical Sciences and Veterinary Public Health, Swedish University of Agricultural Sciences, Uppsala, Sweden.

出版信息

J Vet Pharmacol Ther. 2011 Feb;34(1):64-9. doi: 10.1111/j.1365-2885.2010.01195.x.

Abstract

The pharmacokinetics and analgesic effect of the nonsteroidal anti-inflammatory drug meloxicam (0.5 mg/kg) in goats were investigated. In a randomized, cross-over design the pharmacokinetic parameters were investigated in adult goats (n = 8) after single intravenous and oral administration. The analgesic effect was evaluated in kids using a randomized, placebo controlled and blinded protocol. Kids received meloxicam (n = 6) once daily and their siblings (n = 5) got isotonic NaCl intramuscularly while still anaesthetized after cautery disbudding and injections were repeated on three consecutive days. In the adult goats after intravenous administration the terminal half-life was 10.9 ± 1.7 h, steady-state volume of distribution was 0.245 ± 0.06 L/kg, and total body clearance was 17.9 ± 4.3 mL/h/kg. After oral administration bioavailability was 79 ± 19%, C(max) was 736 ± 184 ng/mL, T(max) was 15 ±5 h, although the terminal half-life was similar to the intravenous value, 11.8 ± 1.7 h. Signs of pain using a visual analogue scale were smaller in kids treated with meloxicam compared with kids treated with placebo on the first day after disbudding, but subsequently no difference in pain was noticeable. Plasma cortisol and glucose concentrations did not differ between the two groups.

摘要

研究了非甾体抗炎药美洛昔康(0.5mg/kg)在山羊体内的药代动力学和镇痛效果。采用随机交叉设计,在成年山羊(n = 8)单次静脉注射和口服给药后研究药代动力学参数。采用随机、安慰剂对照和双盲方案对幼羊的镇痛效果进行评估。幼羊每天接受一次美洛昔康(n = 6),其同胞(n = 5)在烧灼去角后仍处于麻醉状态时肌肉注射等渗氯化钠,连续三天重复注射。成年山羊静脉给药后,末端半衰期为10.9±1.7小时,稳态分布容积为0.245±0.06L/kg,全身清除率为17.9±4.3mL/h/kg。口服给药后生物利用度为79±19%,C(max)为736±184ng/mL,T(max)为15±5小时,尽管末端半衰期与静脉注射值相似,为11.8±1.7小时。去角后第一天,使用视觉模拟评分法,接受美洛昔康治疗的幼羊的疼痛迹象比接受安慰剂治疗的幼羊小,但随后疼痛无明显差异。两组血浆皮质醇和葡萄糖浓度无差异。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验