过氧化物酶体增殖物激活受体-γ 的激活可能抑制糖尿病条件下生物瓣主动脉和主动脉瓣移植物的体内退变。

PPAR-Gamma Activation May Inhibit the In Vivo Degeneration of Bioprosthetic Aortic and Aortic Valve Grafts under Diabetic Conditions.

机构信息

Department of Cardiovascular Surgery, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany.

出版信息

Int J Mol Sci. 2021 Oct 14;22(20):11081. doi: 10.3390/ijms222011081.

Abstract

BACKGROUND

We aimed to examine the anti-calcification and anti-inflammatory effects of pioglitazone as a PPAR-gamma agonist on bioprosthetic-valve-bearing aortic grafts in a rat model of diabetes mellitus (DM).

METHODS

DM was induced in male Wistar rats by high-fat diet with an intraperitoneal streptozotocin (STZ) injection. The experimental group received additional pioglitazone, and controls received normal chow without STZ ( = 20 each group). Cryopreserved aortic donor grafts including the aortic valve were analyzed after 4 weeks and 12 weeks in vivo for analysis of calcific bioprosthetic degeneration.

RESULTS

DM led to a significant media proliferation at 4 weeks. The additional administration of pioglitazone significantly increased circulating adiponectin levels and significantly reduced media thickness at 4 and 12 weeks, respectively ( = 0.0002 and = 0.0107, respectively). Graft media calcification was highly significantly inhibited by pioglitazone after 12 weeks ( = 0.0079). Gene-expression analysis revealed a significant reduction in relevant chondro-osteogenic markers and by pioglitazone at 4 weeks.

CONCLUSIONS

Under diabetic conditions, pioglitazone leads to elevated circulating levels of adiponectin and to an inhibition of bioprosthetic graft degeneration, including lower expression of chondro-osteogenic genes, decreased media proliferation, and inhibited graft calcification in a small-animal model of DM.

摘要

背景

我们旨在研究吡格列酮作为一种过氧化物酶体增殖物激活受体-γ激动剂对糖尿病大鼠模型中生物瓣主动脉移植物的抗钙化和抗炎作用。

方法

雄性 Wistar 大鼠通过高脂肪饮食联合腹腔注射链脲佐菌素(STZ)诱导糖尿病。实验组额外给予吡格列酮,对照组给予不含 STZ 的普通饲料(每组 20 只)。在体内 4 周和 12 周后,对冷冻保存的主动脉供体移植物(包括主动脉瓣)进行分析,以分析钙化生物瓣退行性变。

结果

糖尿病导致 4 周时明显的中膜增殖。额外给予吡格列酮显著增加了循环脂联素水平,并分别在 4 周和 12 周时显著降低了中膜厚度(分别为 = 0.0002 和 = 0.0107)。12 周后,吡格列酮显著抑制移植物中膜钙化(= 0.0079)。基因表达分析显示,吡格列酮在 4 周时显著降低了相关的软骨骨生成标志物 和 。

结论

在糖尿病条件下,吡格列酮可提高循环脂联素水平,并抑制生物瓣移植物退化,包括降低中膜增殖和抑制移植物钙化,这在 DM 的小动物模型中得到了证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24e0/8538504/5da15584961a/ijms-22-11081-g001.jpg

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