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大鼠亚慢性暴露于二苯基二硒醚的毒理学评价

Toxicological evaluation of subchronic exposure to diphenyl diselenide in rats.

作者信息

Meotti Flavia Carla, Borges Vanessa Corralo, Perottoni Juliano, Nogueira Cristina Wayne

机构信息

Laboratório de Síntese, Reatividade e Avaliação Farmacológica e Toxicológica de Organocalcogênios, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, CEP 97105-900, RS, Brazil.

出版信息

J Appl Toxicol. 2008 Jul;28(5):638-44. doi: 10.1002/jat.1315.

Abstract

The aim of this study was to investigate the effects caused by subchronic exposure to diphenyl diselenide in rats. Adult Wistar rats were exposed to diphenyl diselenide (5-300 micromol kg(-1), subcutaneously) once a day for 14 days. The subchronic administration of diphenyl diselenide at a dose of 300 micromol kg(-1) significantly increased aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activities in plasma. Conversely, this exposure did not alter lactate dehydrogenase (LDH) activity, urea and creatinine levels in plasma. The activity of delta-aminolevulinate dehydratase (delta-ALA-D) from liver and kidney was inhibited by high dosages of diphenyl diselenide. Diphenyl diselenide did not alter renal Na(+)/K(+)ATPase. A decline in body weight gain was associated with a decrease in food consumption in rats treated with 100 or 300 micromol kg(-1) diphenyl diselenide. At these dosages (100 and 300 micromol kg(-1)), diphenyl diselenide did not cause histological alterations in the liver of rats. Taken together, these results demonstrated that subchronic exposure to diphenyl diselenide at high doses induced minor toxicological effects.

摘要

本研究的目的是调查大鼠亚慢性暴露于二苯基二硒醚所引起的影响。成年Wistar大鼠每天皮下注射二苯基二硒醚(5 - 300微摩尔/千克),持续14天。以300微摩尔/千克的剂量亚慢性给予二苯基二硒醚可显著提高血浆中天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)的活性。相反,这种暴露并未改变血浆中乳酸脱氢酶(LDH)的活性、尿素和肌酐水平。高剂量的二苯基二硒醚会抑制肝脏和肾脏中δ-氨基乙酰丙酸脱水酶(δ-ALA-D)的活性。二苯基二硒醚不会改变肾脏中的钠钾ATP酶。在接受100或300微摩尔/千克二苯基二硒醚处理的大鼠中,体重增加的下降与食物摄入量的减少有关。在这些剂量(100和300微摩尔/千克)下,二苯基二硒醚不会引起大鼠肝脏的组织学改变。综上所述,这些结果表明高剂量亚慢性暴露于二苯基二硒醚会诱导轻微的毒理学效应。

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