Borges Lysandro P, Nogueira Cristina Wayne, Panatieri Rodrigo B, Rocha João Batista Teixeira, Zeni Gilson
Departamento de Química, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria 97105-900, RS, Brazil.
Chem Biol Interact. 2006 Mar 25;160(2):99-107. doi: 10.1016/j.cbi.2005.12.010. Epub 2006 Jan 30.
The effect of post-treatment with diphenyl diselenide on liver damage induced by 2-nitropropane (2-NP) was examined in male rats. Rats were pre-treated with a single dose of 2-NP (100 mg/kg body weight dissolved in canola oil). Afterward, the animals were post-treated with a dose of diphenyl diselenide (10, 50 or 100 micromol/kg). The parameters that indicate tissue damage such as liver histopathology, plasma aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma-glutamyl transferase (GGT), urea and creatinine were determined. Since the liver damage induced by 2-NP is related to oxidative damage, lipid peroxidation, superoxide dismutase (SOD), catalase (CAT) and ascorbic acid level were also evaluated. Diphenyl diselenide (50 and 100 micromol/kg) effectively restored the increase of ALT and AST activities and urea level when compared to the 2-NP group. At the higher dose, diphenyl diselenide decreased GGT activity. Treatment with diphenyl diselenide, at all doses, effectively ameliorated the increase of hepatic and renal lipid peroxidation when compared to 2-NP group. 2-NP reduced CAT activity and neither alter SOD activity nor ascorbic acid level. This study points out the involvement of CAT activity in 2-NP-induced acute liver damage and suggests that the post-treatment with diphenyl diselenide was effective in restoring the hepatic damage induced by 2-NP.
在雄性大鼠中研究了二苯基二硒化物对2-硝基丙烷(2-NP)诱导的肝损伤的治疗后效果。大鼠预先用单剂量的2-NP(100mg/kg体重,溶于菜籽油)进行处理。之后,动物用一定剂量的二苯基二硒化物(10、50或100微摩尔/千克)进行治疗后处理。测定了指示组织损伤的参数,如肝脏组织病理学、血浆天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、γ-谷氨酰转移酶(GGT)、尿素和肌酐。由于2-NP诱导的肝损伤与氧化损伤有关,还评估了脂质过氧化、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和抗坏血酸水平。与2-NP组相比,二苯基二硒化物(50和100微摩尔/千克)有效地恢复了ALT和AST活性以及尿素水平的升高。在较高剂量时,二苯基二硒化物降低了GGT活性。与2-NP组相比,所有剂量的二苯基二硒化物治疗均有效改善了肝脏和肾脏脂质过氧化的增加。2-NP降低了CAT活性,既未改变SOD活性也未改变抗坏血酸水平。本研究指出了CAT活性在2-NP诱导的急性肝损伤中的作用,并表明二苯基二硒化物的治疗后处理对恢复2-NP诱导的肝损伤有效。