首页> 外文期刊>Drug Design, Development and Therapy >Protective role of quercetin against manganese-induced injury in the liver, kidney, and lung; and hematological parameters in acute and subchronic rat models
【24h】

Protective role of quercetin against manganese-induced injury in the liver, kidney, and lung; and hematological parameters in acute and subchronic rat models

机译:槲皮素对锰引起的肝,肾和肺损伤的保护作用;和亚慢性大鼠模型的血液学和血液学参数

获取原文
       

摘要

Manganese (Mn) is an important mineral element required in trace amounts for development of the human body, while over- or chronic-exposure can cause serious organ toxicity. The current study was designed to evaluate the protective role of quercetin (Qct) against Mn-induced toxicity in the liver, kidney, lung, and hematological parameters in acute and subchronic rat models. Male Sprague Dawley rats were divided into control, Mn (100 mg/kg for acute model and 15 mg/kg for subchronic model), and Mn + Qct (25 and 50 mg/kg) groups in both acute and subchronic models. Our result revealed that Mn + Qct groups effectively reduced Mn-induced ALT, AST, and creatinine levels. However, Mn + Qct groups had effectively reversed Mn-induced alteration of complete blood count, including red blood cells, hemoglobin, hematocrit, mean corpuscular volume, mean corpuscular hemoglobin, mean corpuscular hemoglobin concentration, platelets, and white blood cells. Meanwhile, the Mn + Qct groups had significantly decreased neutrophil and eosinophil and increased lymphocyte levels relative to the Mn group. Additionally, Mn + Qct groups showed a beneficial effect against Mn-induced macrophages and neutrophils. Our result demonstrated that Mn + Qct groups exhibited protective effects on Mn-induced alteration of GRP78, CHOP, and caspase-3 activities. Furthermore, histopathological observation showed that Mn + Qct groups effectively counteracted Mn-induced morphological change in the liver, kidney, and lung. Moreover, immunohistochemically Mn?+ Qct groups had significantly attenuated Mn-induced 8-oxo-2′-deoxyguanosine immunoreactivity. Our study suggests that Qct could be a substantially promising organ-protective agent against toxic Mn effects and perhaps against other toxic metal chemicals or drugs.
机译:锰是人体发育所需的微量必需的重要矿物质元素,而过度或长期暴露会导致严重的器官毒性。本研究旨在评估槲皮素(Qct)在急性和亚慢性大鼠模型中对Mn诱导的肝,肾,肺和血液学参数毒性的保护作用。将雄性Sprague Dawley大鼠分为对照组,急性和亚慢性模型中的Mn(急性模型为100 mg / kg,亚慢性模型为15 mg / kg)和Mn + Qct(25和50 mg / kg)组。我们的结果表明,Mn + Qct组可有效降低Mn诱导的ALT,AST和肌酐水平。但是,Mn + Qct组有效逆转了Mn引起的全血细胞计数的改变,包括红细胞,血红蛋白,血细胞比容,平均红细胞体积,平均红细胞血红蛋白,平均红细胞血红蛋白浓度,血小板和白细胞。同时,与Mn组相比,Mn + Qct组的嗜中性粒细胞和嗜酸性粒细胞明显减少,淋巴细胞水平升高。另外,Mn + Qct基团显示出对Mn诱导的巨噬细胞和嗜中性粒细胞的有益作用。我们的结果表明,Mn + Qct基团对Mn诱导的GRP78,CHOP和caspase-3活性变化具有保护作用。此外,组织病理学观察表明,Mn + Qct基团有效抵消了Mn诱导的肝,肾和肺形态变化。而且,免疫组化的Mn + Qct组显着减弱了Mn诱导的8-oxo-2'-脱氧鸟苷的免疫反应性。我们的研究表明,Qct可能是一种有前途的器官保护剂,可以抵抗有毒的Mn效应,也许还可以抵抗其他有毒的金属化学品或药物。

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