Farias Caio Francisco Santana, Povh Jayme Aparecido, Filho Ruy Alberto Caetano Corrêa, de Araújo Gabriel Andrea Maria, Cardoso Claudia Andrea Lima, da Costa Adryadine Almeida, Oliveira Antônio Francisco, Jerônimo Gabriela Tomas, Martins Maurício Laterça, Ventura Arlene Sobrinho
Aquaculture Department, AQUOS, Aquatic Organisms Health Laboratory, Federal University of Santa Catarina UFSC, Rod. SC 404, Florianópolis, 88040-900, SC, Brazil.
Faculty of Veterinary Medicine and Animal Science- FAMEZ, Federal University of Mato Grosso do Sul UFMS, Av. Sen. Filinto Müller, 2443, 79070-900, Campo Grande, MS, Brazil.
Vet Res Commun. 2025 Apr 17;49(3):168. doi: 10.1007/s11259-025-10739-3.
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 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.
本研究的目的是评估淡水鲳(Piaractus mesopotamicus)幼鱼在浸泡浴接触丁香酚后的药代动力学。平均体重为546.40±74.51 g、全长为25.43±1.52 cm的淡水鲳幼鱼(n = 42)被置于先前溶解在95%乙醇(1:10)中的100 mg/L丁香酚浴中。浸泡10分钟后,将鱼转移到无麻醉的水族箱中恢复。在麻醉后0、0.5、1.0、3.0、6.0、12.0和24.0小时的时间间隔采集血液、肾脏、肌肉、脾脏、鳃和脑样本。使用非房室方法计算药代动力学参数。在所有组织中,麻醉后立即(0小时)记录到最高的丁香酚浓度,从高到低依次为:血浆>肾脏>肌肉>脾脏>鳃>脑。丁香酚在血浆和脑中的半衰期分别为1.12小时和0.73小时,消除常数分别为每小时0.62和0.95。在肌肉和肾脏组织中,半衰期分别为0.14小时和0.09小时,消除常数分别为每小时4.97和7.44。在脾脏和鳃中,半衰期分别为0.21小时和0.23小时,消除常数分别为每小时3.26和3.07。总之,丁香酚在生长阶段的淡水鲳中吸收和消除迅速,麻醉后不久达到峰值浓度,并在24小时内显著降低。