短耐力训练对尼古丁致敏大鼠心脏PINK-1、Parkin和PGC-1α表达水平的影响

A. Lashgari, M. Azarbayjani, M. Peeri, M. Nasehi
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摘要

背景:尼古丁改变心脏中各种基因的表达。粉红色-1(pten诱导的激酶1)是细胞有丝分裂的主要调节因子。此外,Parkin蛋白在泛素化过程中起着关键作用。此外,PGC-1 ι(过氧化物酶体增殖体激活受体γ辅激活因子1- α)是线粒体生物发生的主要调节因子。另一方面,运动对心力衰竭患者有许多积极的生理作用。在这项研究中,我们旨在研究短耐力训练对尼古丁敏感大鼠心脏中parkin、PINK1和PGC- 1 ι基因表达的影响。材料和方法:本研究选用体重约180 ~ 200 gr的雄性Wistar大鼠。小鼠腹腔注射尼古丁0.21 mg/kg。采用Real - time PCR技术检测基因表达情况。结果:烟碱使大鼠PGC-1基因表达降低(p0.05)。短期耐力训练稍微增加了所有基因的表达,但没有统计学意义。结论:短期运动可降低尼古丁诱导的氧化应激的促凋亡和刺激作用。此外,长期运动可能会对线粒体自噬相关基因产生显著的积极影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of short endurance training on the expression level of PINK-1, Parkin and PGC-1α in the heart of nicotine-sensitized rats
Background : Nicotine alters the expression of various genes in the heart. PINK-1(PTEN-induced kinase1) is the major regulator of cellular mitophagy. Moreover, Parkin is a protein that plays a key role in the process of ubiquitination. Also, PGC-1ὰ (peroxisome proliferator-activated receptor gamma coactivator 1-alpha) is the main regulator of mitochondrial biogenesis. On the other hand, exercise has many positive physiological effects on patients suffering from heart failure. In this study, we aimed to investigate the effect of short endurance training on the expression of parkin, PINK1 and PGC- 1ὰ genes in the heart of nicotine-sensitive rats. Materials and methods : in this study, male Wistar rats weighing approximately 180 to 200 gr were used. The animals received nicotine at dose of 0.21 mg/kg intraperitoneally. Real time PCR technique was used to evaluate the expression of genes. Results : The results showed that nicotine decreased the expression of PGC-1ὰ gene (p<0.05) and had no effect on other genes (p>0.05). Short-term endurance training slightly increased the expression of all genes that was not statistically significant. Conclusion : It seems that short-term exercise can reduce the pro–apoptotic and stimulant effects of oxidative stress induced by nicotine. In addition, long-term exercise may potentially induce a significant positive effect on mitophagy-related genes.
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