The Combined Treatment of Curcumin with Verapamil Ameliorates the Cardiovascular Pathology in a Williams-Beuren Syndrome Mouse Model.
Noura AbdallaPaula Ortiz-RomeroIsaac Rodriguez-RoviraLuis Alberto Pérez-JuradoGustavo EgeaVictoria CampuzanoPublished in: International journal of molecular sciences (2023)
Williams-Beuren syndrome (WBS) is a rare disorder caused by a recurrent microdeletion with hallmarks of cardiovascular manifestations, mainly supra-valvular aortic stenosis (SVAS). Unfortunately, there is currently no efficient treatment. We investigated the effect of chronic oral treatment with curcumin and verapamil on the cardiovascular phenotype of a murine model of WBS harbouring a similar deletion, CD (complete deletion) mice. We analysed systolic blood pressure in vivo and the histopathology of the ascending aorta and the left ventricular myocardium to determine the effects of treatments and their underlying mechanism. Molecular analysis showed significantly upregulated xanthine oxidoreductase (XOR) expression in the aorta and left ventricular myocardium of CD mice. This overexpression is concomitant with increased levels of nitrated proteins as a result of byproduct-mediated oxidative stress damage, indicating that XOR-generated oxidative stress impacts the pathophysiology of cardiovascular manifestations in WBS. Only the combined therapy of curcumin and verapamil resulted in a significant improvement of cardiovascular parameters via activation of the nuclear factor erythroid 2 (NRF2) and reduction of XOR and nitrated protein levels. Our data suggested that the inhibition of XOR and oxidative stress damage could help prevent the severe cardiovascular injuries of this disorder.
Keyphrases
- oxidative stress
- left ventricular
- aortic stenosis
- blood pressure
- aortic valve
- mouse model
- heart failure
- nuclear factor
- transcatheter aortic valve replacement
- dna damage
- pulmonary artery
- toll like receptor
- ejection fraction
- ischemia reperfusion injury
- acute myocardial infarction
- coronary artery disease
- diabetic rats
- mitral valve
- left atrial
- poor prognosis
- transcatheter aortic valve implantation
- cardiac resynchronization therapy
- transcription factor
- signaling pathway
- type diabetes
- stem cells
- hypertrophic cardiomyopathy
- immune response
- metabolic syndrome
- hypertensive patients
- insulin resistance
- big data
- uric acid
- cell therapy
- heat shock protein
- amino acid
- high fat diet induced
- protein protein
- percutaneous coronary intervention