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Novel treatments of fibrosis for hypertensive heart disease

Description 
One of the most recognised risk factors for cardiovascular disease is hypertension. Cardiac fibrosis is at the centre of many pathological conditions and a reduction in cardiac fibrosis is now seen as a key factor to improved cardiovascular outcomes. However, there are few treatments that directly ameliorate fibrosis associated with hypertensive heart disease, which may lead to heart failure. Small cardioprotective effects are seen with ACE inhibitors or AT1 receptor antagonists, but these drug classes cannot be given in combination because the adverse effects (hypotension, renal failure) outweigh their potential ability to maximise organ remodelling. Our group has developed the first highly selective series of compounds that stimulate AT2 receptors, part of the ‘cardioprotective arms’ of the renin-angiotensin-system (RAS). This project aims to characterise these compounds either encapsulated in novel injectable hydrogels or as orally-acting derivatives.
Essential criteria: 
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords 
Peptidomimetics, anti-fibrotic drugs, Department of Biochemistry and Molecular Biology
School 
Biomedicine Discovery Institute (School of Biomedical Sciences) » Biochemistry and Molecular Biology
Available options 
PhD/Doctorate
Masters by research
Honours
Time commitment 
Full-time
Physical location 
Biochemistry
Co-supervisors 
Dr 
Mark Del Borgo
Prof 
Rob Widdop

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