Huang W, Lai C C, Wang Y, Askari A, Klevay L M, Askari A, Chiu T H
Medical College of Ohio, Toledo 43699-0008, USA.
Cardiovasc Res. 1995 Apr;29(4):563-8.
The aim was to determine if copper deficiency affects the expression of Na/K-ATPase alpha isoforms in the rat heart.
Copper deficiency was induced by placing weanling rats on a copper deficient diet for 4-5 weeks. Adult ventricular tissue, isolated ventricular myocytes, and brain stems of the control and deficient rats were compared for Cu, Zn-superoxide dismutase (CuZn-SOD) activity and for protein and mRNA contents of Na/K-ATPase alpha isoforms.
In brain stem, where copper deficiency did not alter CuZn-SOD activity, mRNA and protein levels of alpha isoforms also remained unchanged. In ventricular tissue and ventricular myocytes, copper deficiency reduced CuZn-SOD activity, mRNAs of alpha 1 and alpha 2 isoforms, and the alpha 2 isoform protein. The alpha 1 isoform protein of ventricular tissue and its myocytes was marginally reduced by copper deficiency.
In the rat ventricular tissue, oxidative stress resulting from copper deficiency (1) enhances the turnover of the more oxidant sensitive alpha 2 isoform to a greater extent than the turnover of the alpha 1 isoform; (2) regulates mRNA levels of alpha 1 and alpha 2 isoforms; and (3) contributes to the cardiomyopathy of copper deficiency.
确定铜缺乏是否会影响大鼠心脏中钠钾ATP酶α亚型的表达。
通过将断奶大鼠置于缺铜饮食中4 - 5周来诱导铜缺乏。比较对照组和缺铜组大鼠的成年心室组织、分离的心室肌细胞以及脑干中的铜、锌超氧化物歧化酶(CuZn - SOD)活性,以及钠钾ATP酶α亚型的蛋白质和mRNA含量。
在脑干中,铜缺乏未改变CuZn - SOD活性,α亚型的mRNA和蛋白质水平也保持不变。在心室组织和心室肌细胞中,铜缺乏降低了CuZn - SOD活性、α1和α2亚型的mRNA以及α2亚型蛋白质。心室组织及其肌细胞中的α1亚型蛋白质因铜缺乏而略有降低。
在大鼠心室组织中,铜缺乏导致的氧化应激(1)比α1亚型的更新更显著地增强了对氧化更敏感的α2亚型的更新;(2)调节α1和α2亚型的mRNA水平;(3)导致铜缺乏性心肌病。