Residual depletion of eugenol as an anesthetic in growing phase pacu (Piaractus mesopotamicus).

IF 1.8 3区 农林科学 Q2 VETERINARY SCIENCES
Caio Francisco Santana Farias, Jayme Aparecido Povh, Ruy Alberto Caetano Corrêa Filho, Andrea Maria de Araújo Gabriel, Claudia Andrea Lima Cardoso, Adryadine Almeida da Costa, Antônio Francisco Oliveira, Gabriela Tomas Jerônimo, Maurício Laterça Martins, Arlene Sobrinho Ventura
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Abstract

The aim of this study was to evaluate the pharmacokinetics of eugenol in pacu (Piaractus mesopotamicus) juveniles following exposure to an immersion bath. Pacu juveniles (n = 42) with an average weight of 546.40 ± 74.51 g and total length of 25.43 ± 1.52 cm were subjected to a bath with 100 mg L-1 eugenol previously dissolved in 95% ethanol (1:10). After a 10-min immersion, the fish were transferred to anesthetic-free aquaria for recovery. Blood, kidney, muscle, spleen, gills, and brain samples were collected at intervals 0, 0.5, 1.0, 3.0, 6.0, 12.0, and 24.0 h post-anesthesia. Pharmacokinetic parameters were calculated using non-compartmental methods. The highest eugenol concentrations were recorded immediately after anesthesia (0 h) in all tissues, in descending order: plasma > kidney > muscle > spleen > gills > brain. The plasma and brain half-lives of eugenol were 1.12 h and 0.73 h, respectively, with elimination constants of 0.62 and 0.95 per hour. In muscle and kidney tissues, the half-lives were 0.14 h and 0.09 h, with elimination constants of 4.97 and 7.44 per hour, respectively. In the spleen and gills, the half-lives were 0.21 h and 0.23 h, with elimination constants of 3.26 and 3.07 per hour. In conclusion, eugenol is rapidly absorbed and eliminated in growing phase pacu, reaching peak concentrations soon after anesthesia and showing a significant reduction up to 24 h.

丁香酚作为麻醉药在pacu (Piaractus mesopotamicus)生长期的残留损耗。
本研究的目的是评估丁香酚在帕库(Piaractus mesopotamicus)幼体暴露于浸泡浴后的药代动力学。选取42尾平均体重546.40±74.51 g、总长度25.43±1.52 cm的帕库幼鱼,用100 mg L-1的丁香酚浸泡95%乙醇(1:10)。浸泡10分钟后,将鱼转移到无麻醉剂的水族箱中进行恢复。在麻醉后0,0.5,1.0,3.0,6.0,12.0和24.0 h采集血液,肾脏,肌肉,脾脏,鳃和脑样本。采用非区室法计算药代动力学参数。麻醉后即刻(0 h)各组织丁香酚浓度最高,由高到低依次为血浆>肾>肌肉>脾>鳃>脑。丁香酚的血浆半衰期和脑半衰期分别为1.12 h和0.73 h,消除常数为0.62和0.95 / h。在肌肉和肾脏组织中,半衰期分别为0.14 h和0.09 h,消除常数分别为4.97和7.44 / h。脾脏和鳃的半衰期分别为0.21 h和0.23 h,消除常数分别为3.26和3.07 / h。综上所述,丁香酚在生长阶段pacu被迅速吸收和消除,麻醉后很快达到峰值浓度,并在24小时内显著降低。
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
Veterinary Research Communications
Veterinary Research Communications 农林科学-兽医学
CiteScore
2.50
自引率
0.00%
发文量
173
审稿时长
3 months
期刊介绍: Veterinary Research Communications publishes fully refereed research articles and topical reviews on all aspects of the veterinary sciences. Interdisciplinary articles are particularly encouraged, as are well argued reviews, even if they are somewhat controversial. The journal is an appropriate medium in which to publish new methods, newly described diseases and new pathological findings, as these are applied to animals. The material should be of international rather than local interest. As it deliberately seeks a wide coverage, Veterinary Research Communications provides its readers with a means of keeping abreast of current developments in the entire field of veterinary science.
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