Assessment of Hepatotoxic Effects of Quetiapıne at Repeated Doses in Rats

S. Ilgın, D. Burukoğlu, Merve Baysal, Özlem Hinis, Ö. Atlı
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引用次数: 1

Abstract

Quetiapine is an atypical antipsychotic drug used for treatments of patients with schizophrenia. Although hepatotoxic effects related to quetiapine treatment were reported in a few studies, potential hepatotoxicity of this drug was not identified clearly. Therefore, it was aimed to evaluate possible hepatotoxic effects of quetiapine by oral administration of this drug at 10 and 20 mg/kg doses to rats for 30 days in our study. For this purpose, plasma aspartate aminotransferase, alanine aminotransferase, total bilirubin and direct bilirubin levels as markers of hepatotoxicity were determined and histopathological examination was performed in liver tissues. According to our results, serum aspartate aminotransferase and alanine aminotransferase levels were significantly increased in quetiapine-administered groups, whereas total and direct bilirubin levels were significantly increased in high dose group. Histopathological examination of liver tissue indicated that necrotic areas were observed in 10 mg/kg quetiapine-administered group whereas necrotic areas were present and sinusoidal dilatation was observed in 20 mg/kg quetiapine-administered group. According to these results, we concluded that quetiapine may induced hepatotoxic effects in rats, dose-dependently.
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Quetiapıne对大鼠重复剂量肝毒性作用的评价
奎硫平是一种用于治疗精神分裂症患者的非典型抗精神病药物。虽然在一些研究中报道了与喹硫平治疗相关的肝毒性作用,但该药物的潜在肝毒性尚未明确确定。因此,本研究旨在评价喹硫平在30天内以10和20 mg/kg剂量口服给药的肝毒性作用。为此,测定血浆天冬氨酸转氨酶、丙氨酸转氨酶、总胆红素和直接胆红素水平作为肝毒性标志物,并对肝组织进行组织病理学检查。结果显示,喹硫平组大鼠血清天冬氨酸转氨酶和丙氨酸转氨酶水平显著升高,高剂量组大鼠血清总胆红素和直接胆红素水平显著升高。肝组织病理检查显示,10 mg/kg喹硫平组肝组织出现坏死区,20 mg/kg喹硫平组肝组织出现坏死区,肝窦扩张。根据这些结果,我们认为喹硫平可能引起大鼠肝毒性作用,且具有剂量依赖性。
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