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Int J Mol Sci ; 22(20)2021 Oct 14.
Article in English | MEDLINE | ID: mdl-34681744

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 (n = 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 (p = 0.0002 and p = 0.0107, respectively). Graft media calcification was highly significantly inhibited by pioglitazone after 12 weeks (p = 0.0079). Gene-expression analysis revealed a significant reduction in relevant chondro-osteogenic markers osteopontin and RUNX-2 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.


Subject(s)
Aorta/drug effects , Diabetes Mellitus, Experimental/complications , Heart Valve Prosthesis/adverse effects , PPAR gamma/metabolism , Pioglitazone/pharmacology , Animals , Aorta/physiopathology , Aortic Valve/pathology , Aortic Valve Stenosis/etiology , Aortic Valve Stenosis/therapy , Blood Glucose/metabolism , Body Weight , Calcinosis/etiology , Calcinosis/therapy , Diabetes Mellitus, Experimental/blood , Diabetes Mellitus, Experimental/drug therapy , Gene Expression Regulation/drug effects , Materials Testing , Rats, Wistar
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