...
首页> 外文期刊>Human and Experimental Toxicology >Histopathologic changes in liver and renal tissues induced by Ochratoxin A and melatonin in rats.
【24h】

Histopathologic changes in liver and renal tissues induced by Ochratoxin A and melatonin in rats.

机译:ch曲霉毒素A和褪黑激素诱导的大鼠肝脏和肾脏组织的组织病理学变化。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Nephrotoxicity and hepatotoxicity induced by Ochratoxin A (OTA) and ameliorating effects of melatonin were investigated in rats exposed to OTA. Experimental groups were as follows: control; OTA-treated; and OTA plus melatonin (MEL)-treated (OTA+MEL). The rats in the control group were administered with only a daily oral administration of 0.5 M NaHCO3. OTA was administered with a dose of 289 microg/kg in the same way. OTA and MEL were administered orally with OTA (289 microg/kg) and melatonin (10 mg/kg) in two different periods of time during the same day. The histopathologic changes in the liver and kidney tissues of control, OTA and OTA+MEL-treated rats were examined. There were no significant changes in the kidney and liver tissues of the control rats. Significant histopathologic changes were found in the kidney and liver tissue of rats treated with OTA. These were granular or vacuolated degeneration and necrosis of the liver cells, sinusoidal and central vein dilatation, bile duct proliferation, enlargement of periportal areas with mononuclear cell inflammatory infiltration and mild degree fibrous tissue proliferation, tubular epithelial cells degeneration, necrosis, proliferation and karyomegaly in the epithelial cells nuclei and peritubular and periglomerular lymphocyte infiltration, stromal fibrous tissue proliferation, hyperemic vessels. The severity of the lesions was significantly reduced by administration of melatonin. These results revealed that OTA induced significant histopathologic changes in liver and kidney tissue advocating OTA toxicity (P < 0.001), and administration of MEL+OTA significantly reduced the toxic effect of OTA on kidney and liver tissue of rats (P > 0.05).
机译:在暴露于OTA的大鼠中研究了induced曲毒素A(OTA)诱导的肾毒性和肝毒性以及褪黑激素的改善作用。实验组如下:对照组;对照组。经OTA处理;和OTA加褪黑素(MEL)处理(OTA + MEL)。对照组中的大鼠仅每天口服0.5M NaHCO 3。以相同的方式以289微克/千克的剂量给予OTA。在同一天的两个不同时间段内,口服OTA和MEL与OTA(289 microg / kg)和褪黑激素(10 mg / kg)。检查了对照,OTA和OTA + MEL处理的大鼠的肝和肾组织的组织病理学变化。对照大鼠的肾脏和肝脏组织没有明显变化。在用OTA处理的大鼠的肾脏和肝脏组织中发现了明显的组织病理学变化。这些是肝细胞的颗粒或空泡变性和坏死,正弦和中央静脉扩张,胆管增生,具有单核细胞炎性浸润和轻度纤维组织增生的周围区域扩大,肾小管上皮细胞变性,坏死,增生和核仁增生上皮细胞核及肾小管周围和肾小球周围淋巴细胞浸润,间质纤维组织增生,充血性血管。褪黑激素的施用可显着降低病变的严重程度。这些结果表明,OTA诱导了肝和肾组织的显着组织病理学改变,从而引起了OTA毒性(P <0.001),而MEL + OTA的给药显着降低了OTA对大鼠肾脏和肝组织的毒性作用(P> 0.05)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号