【24h】

Effect of diabetes on the tissular Zn/Cu ratio.

机译:糖尿病对组织锌/铜比的影响。

获取原文
获取原文并翻译 | 示例
       

摘要

One of the parameters related to the development of coronary disease in diabetic patients is the tissular Zn/Cu ratio. We evaluated the levels of Zn and Cu, and the Zn/Cu ratio in insulin target tissues in diabetic and normoglucemic growing Wistar rats in order to determine the influence of diabetes and the disease evolution period. Diabetes was induced chemically by administration of streptozotocin. In order to determine the influence of the duration of diabetes on the Zn/Cu ratio, three time periods were studied: 7, 21 and 60 days. The animals were subsequently sacrificed and the target tissues (liver, adipose tissue, and skeletal muscle) were removed. Zn and Cu levels were measured by AAS after wet mineralization. STZ-induced diabetes modified the tissular Zn and Cu content. There was a significant decrease (p < 0.01) in liver and adipose tissue, but not in skeletal muscle. The in adipose tissue and skeletal muscle, but not in liver, effects were dependent on the duration of diabetes. The Cu content was higher in the liver of diabetic rats (p < 0.1) and lower in adipose tissue (p < 0.1) and skeletal muscle (NS). Tissular Cu levels also were affected significantly by the duration of diabetes. The Zn/Cu ratio showed a generalized decrease, except in skeletal muscle. This decrease was dependent on the presence of diabetes mellitus and the duration of the disease (p < 0.01).
机译:与糖尿病患者冠状动脉疾病发展相关的参数之一是组织中的锌/铜比。我们评估了糖尿病和正常血糖生长的Wistar大鼠中胰岛素靶组织中锌和铜的含量以及锌/铜比,以确定糖尿病的影响和疾病发展时期。通过施用链脲佐菌素化学诱导糖尿病。为了确定糖尿病持续时间对锌/铜比的影响,研究了三个时间段:7、21和60天。随后处死动物,并去除目标组织(肝脏,脂肪组织和骨骼肌)。湿矿化后,通过AAS测定锌和铜的含量。 STZ诱发的糖尿病改变了组织中锌和铜的含量。肝脏和脂肪组织显着减少(p <0.01),但骨骼肌无明显减少。脂肪组织和骨骼肌的作用,而不是肝脏的作用,取决于糖尿病的持续时间。糖尿病大鼠肝脏中的铜含量较高(p <0.1),而脂肪组织和骨骼肌(NS)中的铜含量较低。糖尿病持续时间也显着影响了前庭铜水平。锌/铜比普遍下降,骨骼肌除外。这种减少取决于糖尿病的存在和疾病的持续时间(p <0.01)。

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