Gene Expression of GSK3 in Type II Diabetics Compared to Non-Diabetics (ex vivo)

Somayeh Alsadat Hosseini Khorami, M. Mutalib, M. Shiraz, Joseph Anthony Abdullah, Zulida Rejali, R. M. Ali, H. Khaza’ai
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Abstract

GSK3 is a serine/threonine kinase that is involved in the storage of glucose into glycogen through the negative regulation of glycogen synthase. Defects in GSK3 and glycogen synthase function are early stages of the development of insulin resistance, which may cause impaired glycogen synthesis in Type II diabetes. In this cross-sectional study, the gene expression level of GSK3 from Type II diabetic and non-diabetic participants was compared via real-time RT-PCR. To investigate the relationships between GSK3 expression and indicators of insulin resistance, Pearson's correlation analysis was performed. To compare the differences between GSK3 expression levels based on BMI categories, one-way ANOVA was used. Gene expression of GSK3 was slightly higher in diabetic participants compared to non-diabetics, but it was statistically insignificant. Also, no significant difference was found based on BMI categories in the two groups. No significant association between GSK3 expression and indicators of insulin resistance was observed in non-diabetic participants. There was only a positive significant correlation between GSK3 expression and FBS in diabetic participants. These results indicate that the regulation of GSK3 may occur at the translation level, as gene expression level was unaltered between diabetic and non-diabetic participants. Also, since circulating levels of both glucose and insulin regulate GSK3 activity, tissue specificity for the expression and post-translation regulations of GSK3 may exist, which cause hyperactivation or overexpression in some target tissues in diabetes. Furthermore, it is probable that glycogen synthase activity is also regulated by non-insulin mediated mechanisms like exercise or allosteric changes, independent of GSK3 expression.
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2型糖尿病患者与非糖尿病患者GSK3基因的离体表达
GSK3是一种丝氨酸/苏氨酸激酶,通过糖原合成酶的负调控参与将葡萄糖储存为糖原。GSK3和糖原合成酶功能的缺陷是胰岛素抵抗发展的早期阶段,这可能导致II型糖尿病糖原合成受损。在这项横断面研究中,通过实时RT-PCR比较了II型糖尿病和非糖尿病参与者的GSK3基因表达水平。为探讨GSK3表达与胰岛素抵抗指标的关系,采用Pearson相关分析。为了比较基于BMI分类的GSK3表达水平的差异,采用单因素方差分析。GSK3基因在糖尿病患者中的表达略高于非糖尿病患者,但差异无统计学意义。此外,两组在BMI分类上也没有发现显著差异。在非糖尿病参与者中,未观察到GSK3表达与胰岛素抵抗指标之间的显著关联。在糖尿病患者中,GSK3的表达与FBS之间只有显著的正相关。这些结果表明,GSK3的调控可能发生在翻译水平,因为基因表达水平在糖尿病和非糖尿病参与者之间没有改变。此外,由于循环中的葡萄糖和胰岛素水平都能调节GSK3的活性,因此可能存在GSK3表达和翻译后调控的组织特异性,从而导致糖尿病的一些靶组织过度激活或过度表达。此外,糖原合成酶活性也可能受非胰岛素介导的机制调节,如运动或变构变化,独立于GSK3的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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