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Modeling and Evaluation of Murine Diabetic Cardiomyopathy Model
Published on: November 29, 2024
Diabetic Cardiomyopathy: An Update of Mechanisms Contributing to This Clinical Entity
Guanghong Jia1, Michael A Hill1, James R Sowers2
1From the Diabetes and Cardiovascular Research Center (G.J., J.R.S.) and Department of Medical Pharmacology and Physiology (M.A.H., J.R.S.), University of Missouri School of Medicine, Columbia; Dalton Cardiovascular Research Center, University of Missouri, Columbia (M.A.H., J.R.S.); and Research Service, Truman Memorial Veterans Hospital, Columbia, MO (G.J., J.R.S.).
Insights
Diabetic cardiomyopathy, a growing concern linked to diabetes mellitus, causes heart dysfunction through fibrosis and remodeling. Understanding its molecular causes is key to developing new treatments.
Area of Science:
- Cardiology
- Endocrinology
- Molecular Medicine
Background:
- Heart failure is rising, particularly in patients with diabetes mellitus, who face worse outcomes.
- Diabetic cardiomyopathy is characterized by myocardial dysfunction independent of traditional cardiovascular risk factors.
- Its prevalence parallels the increasing rates of diabetes mellitus.
Purpose of the Study:
- To review the instigators of diabetic cardiomyopathy.
- To provide a contemporary view of its development and progression.
- To discuss mechanistically based prevention and treatment strategies.
Main Methods:
- Review of current literature on diabetic cardiomyopathy.
- Analysis of molecular and cellular mechanisms.
- Synthesis of pathophysiological pathways.
Main Results:
- Diabetic cardiomyopathy involves myocardial fibrosis, diastolic and systolic dysfunction.
- Key implicated mechanisms include impaired insulin signaling, mitochondrial dysfunction, oxidative stress, and inflammation.
- Molecular pathways affected include AMP-activated protein kinase, peroxisome proliferator-activated receptors, and O-linked N-acetylglucosamine.
Conclusions:
- Diabetic cardiomyopathy is a complex condition with multifactorial origins.
- Targeting specific molecular and metabolic pathways offers potential for therapeutic intervention.
- Further research is needed to translate mechanistic insights into effective clinical strategies.
Abstract:
Heart failure and related morbidity and mortality are increasing at an alarming rate, in large part, because of increases in aging, obesity, and diabetes mellitus. The clinical outcomes associated with heart failure are considerably worse for patients with diabetes mellitus than for those without diabetes mellitus. In people with diabetes mellitus, the presence of myocardial dysfunction in the absence of overt clinical coronary artery disease, valvular disease, and other conventional cardiovascular risk factors, such as hypertension and dyslipidemia, has led to the descriptive terminology, diabetic cardiomyopathy. The prevalence of diabetic cardiomyopathy is increasing in parallel with the increase in diabetes mellitus. Diabetic cardiomyopathy is initially characterized by myocardial fibrosis, dysfunctional remodeling, and associated diastolic dysfunction, later by systolic dysfunction, and eventually by clinical heart failure. Impaired cardiac insulin metabolic signaling, mitochondrial dysfunction, increases in oxidative stress, reduced nitric oxide bioavailability, elevations in advanced glycation end products and collagen-based cardiomyocyte and extracellular matrix stiffness, impaired mitochondrial and cardiomyocyte calcium handling, inflammation, renin-angiotensin-aldosterone system activation, cardiac autonomic neuropathy, endoplasmic reticulum stress, microvascular dysfunction, and a myriad of cardiac metabolic abnormalities have all been implicated in the development and progression of diabetic cardiomyopathy. Molecular mechanisms linked to the underlying pathophysiological changes include abnormalities in AMP-activated protein kinase, peroxisome proliferator-activated receptors, O-linked N-acetylglucosamine, protein kinase C, microRNA, and exosome pathways. The aim of this review is to provide a contemporary view of these instigators of diabetic cardiomyopathy, as well as mechanistically based strategies for the prevention and treatment of diabetic cardiomyopathy.
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