PDCD4 knockdown protected against left ventricular remodeling, dysfunction, and insulin resistance in type 2 diabetic cardiomyopathy rats via the PI3K-AKT pathway.
Does PDCD4 knockdown improve left ventricular remodeling, dysfunction, and insulin resistance in a rat model of type 2 diabetic cardiomyopathy?
PDCD4 knockdown protects against left ventricular remodeling, dysfunction, and insulin resistance in a rat model of type 2 diabetic cardiomyopathy, potentially via the PI3K-AKT pathway.
OBJECTIVE: Diabetic cardiomyopathy (DCM) is characterized by cardiac remodeling, dysfunction, and insulin resistance; however, the underlying mechanism has not been fully elucidated. Programmed cell death 4 (PDCD4) is a novel inflammation and apoptosis gene, but its role in type 2 DCM remains elusive. We aimed to determine if PDCD4 intervention improves DCM by affecting left ventricular remodeling, function, and insulin resistance. RESEARCH DESIGN AND METHODS: rat, established a type 2 diabetes animal model, and constructed a PDCD4 overexpressed adenovirus and PDCD4 small interfer RNA (siRNA) vectors to alter PDCD4 expression in H9c2 cardiomyocytes. Thereafter, glucose levels, lipid metabolism, echocardiography, and extent of myocardial fibrosis, inflammation, and apoptosis were compared in vivo and in vitro. RESULTS: PDCD4 deficiency improved insulin resistance, cardiac remodeling, and dysfunction in type 2 DCM rats and improved myocardial hypertrophy, fibrosis, inflammation, and apoptosis. Proliferation and transformation of cardiac fibroblasts was reduced via PDCD4 downregulation in vitro under high-glucose stimulation. Furthermore, PDCD4 regulated the myocardial phosphatidylinositol 3-kinase-protein kinase B (PI3K-AKT) pathway in vivo and in vitro. PDCD4 intervention affected cardiac remodeling, dysfunction, and insulin resistance by influencing fibrosis, inflammation, and apoptosis via the PI3K-AKT pathway in vivo. CONCLUSIONS: PDCD4 knockdown protected against left ventricular remodeling, dysfunction, and insulin resistance in type 2 DCM rats. The underlying mechanisms may involve reducing cardiomyocyte apoptosis, inflammation, fibrosis, and normalized PI3K-AKT phosphorylation. To the best of our knowledge, our study is the first to report the effects and underlying mechanisms of PDCD4 in type 2 DCM. These results provide a potential new treatment avenue for improving the prognosis of patients with type 2 DCM.
Zhang et al. (Wed,) conducted a other in Type 2 diabetic cardiomyopathy. PDCD4 knockdown (siRNA) vs. Control was evaluated on Left ventricular remodeling, function, and insulin resistance. PDCD4 knockdown protected against left ventricular remodeling, dysfunction, and insulin resistance in type 2 diabetic cardiomyopathy rats via the PI3K-AKT pathway.