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首页> 外文期刊>Environmental toxicology and pharmacology >Association of inflammatory response and oxidative injury in the pathogenesis of liver steatosis and insulin resistance following subchronic exposure to malathion in rats
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Association of inflammatory response and oxidative injury in the pathogenesis of liver steatosis and insulin resistance following subchronic exposure to malathion in rats

机译:亚慢性暴露于马拉硫磷后大鼠肝脂肪变性和胰岛素抵抗中炎症反应和氧化损伤的相关性

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摘要

Insulin resistance and risk of type 2 diabetes are the most important complications following exposure to organophosphorous (OPs) pesticides. Regarding the importance of liver on metabolic pathways regulation, in particular blood glucose homeostasis, we focused on liver inflammation and oxidative damages in a subchronic model of toxicity by malathion. Adult male Wistar rats of body weight 200-250 g were used for the study. Malathion (200 mg/kg b.w./day) was administered to rats by oral intubation for 28 days. Glycemic and insulin resistance indices, markers of liver injury, markers of inflammation and oxidative stress were assessed. Malathion-treated rats showed increased glycemia, insulinemia and glycated hemoglobin level, HOMA-IR and HOMA-β indices, plasma activities of hepatocel-lular enzymes, lipid peroxidation index, CD3~+/CD4~+ and CD3~+/CD4~+ and pro-inflammatory cytokines when decreased antioxidant status in liver was noted. Most of our study indicates that malathion promotes insulin resistance, inflammation and Hepatosteatosis in subchronic model of exposure. On the basis of biochemical and molecular findings, it is concluded that insulin resistance induced by malathion occurs through oxidative stress and related pro-inflammatory markers in a way to result in a reduced function of insulin in liver cells.
机译:接触有机磷(OPs)农药后,胰岛素抵抗和2型糖尿病的风险是最重要的并发症。关于肝脏在代谢途径调节中的重要性,特别是血糖稳态,我们在马拉硫磷引起的亚慢性毒性模型中关注肝脏炎症和氧化损伤。研究使用体重为200-250 g的成年雄性Wistar大鼠。通过口服插管法向大鼠施用马拉硫磷(200 mg / kg体重/天),持续28天。评估了血糖和胰岛素抵抗指数,肝损伤指标,炎症指标和氧化应激指标。马拉硫磷治疗的大鼠血糖,胰岛素血症和糖化血红蛋白水平,HOMA-IR和HOMA-β指数,肝细胞酶的血浆活性,脂质过氧化指数,CD3〜+ / CD4〜+和CD3〜+ / CD4〜+升高并观察到肝脏中的抗氧化剂状态降低时,促炎细胞因子的含量升高。我们的大多数研究表明,马拉松在亚慢性暴露模型中会促进胰岛素抵抗,炎症和肝脂肪变性。根据生化和分子发现,可以得出结论,马拉硫磷诱导的胰岛素抵抗是通过氧化应激和相关的促炎标记物发生的,从而导致胰岛素在肝细胞中的功能降低。

著录项

  • 来源
    《Environmental toxicology and pharmacology》 |2014年第2期|542-553|共12页
  • 作者单位

    Laboratory of Aggression Physiology and Endocrine Metabolic Studies, Department of Biology, Faculty of Sciences, El Manar University Tunis, Tunisia;

    Laboratory of Aggression Physiology and Endocrine Metabolic Studies, Department of Biology, Faculty of Sciences, Tunis, Tunisia,Laboratory of Clinical Immunology, Pasteur Institute of Tunis, Tunis, Tunisia;

    Laboratory of Clinical Biochemistry, Charles Nicolle Hospital, Tunis, Tunisia;

    Laboratory of Aggression Physiology and Endocrine Metabolic Studies, Department of Biology, Faculty of Sciences, Tunis, Tunisia;

    Laboratory of Aggression Physiology and Endocrine Metabolic Studies, Department of Biology, Faculty of Sciences, Tunis, Tunisia;

    Laboratory of Clinical Immunology, Pasteur Institute of Tunis, Tunis, Tunisia;

    Laboratory of Clinical Immunology, Pasteur Institute of Tunis, Tunis, Tunisia;

    Laboratory of Aggression Physiology and Endocrine Metabolic Studies, Department of Biology, Faculty of Sciences, Tunis, Tunisia;

    Laboratory of Clinical Biochemistry, Charles Nicolle Hospital, Tunis, Tunisia;

    Laboratory of Aggression Physiology and Endocrine Metabolic Studies, Department of Biology, Faculty of Sciences, Tunis, Tunisia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Malathion; Insulin resistance; Inflammation; Oxidative stress; Hepatosteatosis;

    机译:马拉硫磷胰岛素抵抗;炎;氧化应激肝脂肪变性;

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