University Research Lecturer
Diabetes mellitus is a major cause of death and disability and a large economic burden on health care systems across the world. Globally, 1 in 12 all-cause deaths in adults have been attributed to diabetes and its complications. Epidemiological data suggest that diabetes may in itself give rise to a specific cardiomyopathy characterized by progressively impaired left ventricular (LV) diastolic function and, in humans, a predominant phenotype of heart failure with preserved ejection fraction (HFpEF). Despite current glucose lowering therapies, diabetic patients are still at higher risk of developing heart disease.
Excessive production of reactive oxygen species, metabolic disturbances (eg alterations in substrate supply or utilisation), remodelling of the extracellular matrix, and mitochondrial dysfunction have been advocated as main determinants of both vascular and myocardial dysfunction in diabetes. However, a unifying mechanism upstream of the observed LV functional changes is still missing.
I have investigated the molecular signature of diabetes in heart cells/muscle of patients and animal models and discovered that cardiac dysfunction is prevented by increasing the myocardial level of tetrahydrobiopterin (BH4). BH4 is a key cofactor of nitric oxide synthase (NOS), and is responsible for maintaining the enzyme’s function in the presence of oxidative stress. These findings open the possibility that BH4 supplementation may provide a novel therapeutic tool in the management of patients with diabetes and HFpEF.
The aim of my research is to elucidate the mechanisms by which BH4 protects the cardiovascular system in diabetes. We are currently assessing the antioxidant properties of BH4 as well as its effects on metabolism and the inflammatory responses at different stages of the disease.
Tetrahydrobiopterin Protects Against Hypertrophic Heart Disease Independent of Myocardial Nitric Oxide Synthase Coupling.
Hashimoto T. et al, (2016), J Am Heart Assoc, 5
Nitric oxide synthase regulation of cardiac excitation-contraction coupling in health and disease.
Simon JN. et al, (2014), J Mol Cell Cardiol, 73, 80 - 91
Cardiomyocyte GTP cyclohydrolase 1 and tetrahydrobiopterin increase NOS1 activity and accelerate myocardial relaxation
Carnicer R. et al, (2012), Circulation Research, 111, 718 - 727
Improved cellular uptake of perfluorocarbon nanoparticles for in vivo murine cardiac 19F MRS/MRI and temporal tracking of progenitor cells.
Constantinides C. et al, (2019), Nanomedicine, 18, 391 - 401
BH4 SUPPLEMENTATION AS A NEW TREATMENT FOR DIABETIC CARDIOMYOPATHY
Carnicer R. et al, (2019), HEART, 105, A153 - A153
Correction: Fast, quantitative, murine cardiac 19F MRI/MRS of PFCE-labeled progenitor stem cells and macrophages at 9.4T.
Constantinides C. et al, (2019), PLoS One, 14
In Vivo Tracking and 1H/19F Magnetic Resonance Imaging of Biodegradable Polyhydroxyalkanoate/Polycaprolactone Blend Scaffolds Seeded with Labeled Cardiac Stem Cells.
Constantinides C. et al, (2018), ACS Appl Mater Interfaces, 10, 25056 - 25068
DIABETES-INDUCED INNATE IMMUNE MEMORY DRIVES INFLAMMATION AND ATHEROSCLEROSIS, DESPITE RESTORATION OF NORMOGLYCAEMIA
Edgar L. et al, (2018), HEART, 104, A111 - A111