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部分 HIF-1α 缺乏会刺激链脲佐菌素诱导的糖尿病小鼠的病理性心脏变化。

Partial deficiency of HIF-1α stimulates pathological cardiac changes in streptozotocin-induced diabetic mice.

机构信息

Institute of Biotechnology AS CR, Prague, Czechia.

出版信息

BMC Endocr Disord. 2014 Feb 6;14:11. doi: 10.1186/1472-6823-14-11.

Abstract

BACKGROUND

Diabetic cardiomyopathy is associated with a number of functional and structural pathological changes such as left ventricular dysfunction, cardiac remodeling, and apoptosis. The primary cause of diabetic cardiomyopathy is hyperglycemia, the metabolic hallmark of diabetes. Recent studies have shown that a diabetic environment suppresses hypoxia-inducible factor (HIF)-1α protein stability and function. The aim of this study was to analyze the functional role of HIF-1α in the development of diabetic cardiomyopathy. We have hypothesized that the partial deficiency of HIF-1α may compromise cardiac responses under diabetic conditions and increase susceptibility to diabetic cardiomyopathy.

METHODS

Diabetes was induced by streptozotocin in wild type (Wt) and heterozygous Hif1a knock-out (Hif1a+/-) mice. Echocardiographic evaluations of left ventricular functional parameters, expression analyses by qPCR and Western blot, and cardiac histopathology assessments were performed in age-matched groups, diabetic, and non-diabetic Wt and Hif1a+/- mice.

RESULTS

Five weeks after diabetes was established, a significant decrease in left ventricle fractional shortening was detected in diabetic Hif1a+/- but not in diabetic Wt mice. The combination effects of the partial deficiency of Hif1a and diabetes affected the gene expression profile of the heart, including reduced vascular endothelial growth factor A (Vegfa) expression. Adverse cardiac remodeling in the diabetic Hif1a+/- heart was shown by molecular changes in the expression of structural molecules and components of the extracellular matrix.

CONCLUSIONS

We have shown a correlation between heterozygosity for Hif1α and adverse functional, molecular, and cellular changes associated with diabetic cardiomyopathy. Our results provide evidence that HIF-1α regulates early cardiac responses to diabetes, and that HIF-1α deregulation may influence the increased risk for diabetic cardiomyopathy.

摘要

背景

糖尿病心肌病与许多功能和结构病理变化有关,如左心室功能障碍、心脏重构和细胞凋亡。糖尿病心肌病的主要原因是高血糖,这是糖尿病的代谢标志。最近的研究表明,糖尿病环境会抑制缺氧诱导因子 (HIF)-1α 蛋白的稳定性和功能。本研究旨在分析 HIF-1α 在糖尿病心肌病发展中的功能作用。我们假设 HIF-1α 的部分缺失可能会影响糖尿病条件下的心脏反应,并增加患糖尿病心肌病的易感性。

方法

链脲佐菌素诱导野生型 (Wt) 和杂合型 Hif1a 敲除 (Hif1a+/-) 小鼠发生糖尿病。在年龄匹配的 Wt 和 Hif1a+/- 小鼠的糖尿病和非糖尿病组中,进行左心室功能参数的超声心动图评估、qPCR 和 Western blot 表达分析以及心脏组织病理学评估。

结果

在糖尿病确立 5 周后,在糖尿病 Hif1a+/- 小鼠中检测到左心室短轴缩短分数显著下降,但在糖尿病 Wt 小鼠中未检测到。Hif1a 部分缺失和糖尿病的联合作用影响了心脏的基因表达谱,包括血管内皮生长因子 A (Vegfa) 表达的降低。糖尿病 Hif1a+/- 心脏的不良心脏重构表现为结构分子和细胞外基质成分表达的分子变化。

结论

我们已经证明了 Hif1α 杂合性与糖尿病心肌病相关的不良功能、分子和细胞变化之间存在相关性。我们的研究结果表明 HIF-1α 调节心脏对糖尿病的早期反应,而 HIF-1α 失调可能会影响糖尿病心肌病风险的增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4417/3922431/6ba993aec209/1472-6823-14-11-1.jpg

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