Arpeeta Sharma
Monash University, Baker Heart and Diabetes Institute, Centre for Heart Lung Innovation
Research areas: Biochemistry, Genetics and Molecular Biology · Molecular Biology · Nitric Oxide and Endothelin Effects · Caveolin-1 and cellular processes · Angiogenesis and VEGF in Cancer
About
Dr Arpeeta Sharma leads a research program looking at novel therapeutic targets for diabetes-associated cardiovascular diseases. She holds a BSc Hons (King’s College, London) and a Master's and PhD in Pharmacology from University of British Columbia, Vancouver, Canada (2014). Dr Sharma was a Group Leader of the Cardiovascular Inflammation and Redox Biology Laboratory at the Baker Institute (Melbourne) before joining the Department of Diabetes at the School of Translational Medicine, Monash University as a Research Fellow in 2022. Dr Sharma has a proven track record in cardiovascular biology (38 publications; 1365 citations and a h-index=18). In the last 5 years, she has published 5 papers in the field of cardiovascular as a leading author. Dr Sharma has successfully led and completed numerous preclinical studies (~400 mice per study) using a variety of mouse models to study diabetes-induced cardiovascular complications for both grant-funded and industry-funded (Reata, Visterra and Bayer) projects. Her work has led to a NHMRC Early Career Fellowship (2015-2019) and independent project funding by NHMRC (CIC; IDEAS grant 2024-2027); Diabetes Australia (CIA 2019, 2022, 2023; >$200K) and pharmaceutical companies such as Bayer (CIA 2019; $130K). Dr Sharma has a growing international presence and is the inaugural recipient of the CSANZ-ACvA-ESC Ambassador Fellowship (Cardiovascular Society of Australia and New Zealand –Australian Cardiovascular Alliance–European Society of Cardiology) and an executive member of the Australian Atherosclerosis Society.
In her PhD, Dr Sharma characterised a peptide that could up-regulate the release of protective nitric oxide, the first specific peptide of its kind, which is now undergoing chemical screening in Phase I clinical trials. In 2015, Dr Sharma was awarded the NHMRC Peter Doherty Early Career Fellowship to explore key antioxidant and anti-inflammatory pathways involved in diabetes-induced vascular disease as well as therapeutics to limit cellular damage, without triggering detrimental side effects.
Dr Sharma has also previously demonstrated the NLRP3 inflammasome pathway exacerbates diabetes-induced cardiovascular complications and has shown the correlation between infiltrating immune cells and cardiovascular injury in preclinical models of diabetes. Currently, her work is focussing on complement C5a receptor modulation in the diabetic heart and RNA therapy for various targets involved in diabetes-associated vascular complications. Dr Sharma is trained in the generation of animal models of diabetes, assessment of cardiac and endothelial function, live tissue assays for measurement of inflammation and assessment leukocyte trafficking by flow cytometry.
Employment
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Monash University Research Officer2022 - Present
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Baker IDI Heart and Diabetes Institute Post-doctoral researcher2014 - 2022
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Baker IDI Heart and Diabetes Institute PhD student2011 - 2014
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Centre for Heart Lung Innovation MSc and PhD student2008 - 2011
Education
Education history is unavailable.
Projects & Funding
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Inhibiting Complement C5a Receptors to Improve Heart Function in Type 2 Diabetes Diabetes Australia2023 - 2024
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Modulating soluble guanylate cyclase activity to improve type 2 diabetic and hypertensive heart function. Diabetes Australia2022 - 2023
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Characterisation of a novel mouse model to study diabetes and hypertension Baker Heart and Diabetes Institute2021 - 2021
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Targeting the inflammasome to ameliorate Type 2 Diabetic cardiac and vascular diseases. Diabetes Australia2019 - 2020
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Ameliorating diabetes-associated atherosclerosis and diabetic nephropathy through modulation of soluble guanylate cyclase Bayer (Germany)2019 - 2021
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Dissecting the angiogenic potential of Nrf2 in the diabetic setting Baker Heart and Diabetes Institute2018 - 2018
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Investigating the role of Nrf2 activation in diabetes-induced endothelial dysfunction. NHMRC2015 - 2019
Publications (49)
- The Role of Activator Protein-1 Complex in Diabetes-Associated Atherosclerosis: Insights From Single-Cell RNA Sequencing. Save
- Selectively targeting Gasdermin-D attenuates inflammation and fibrosis in the heart after ischemia reperfusion injury. Save
- Selectively targeting Gasdermin-D attenuates inflammation and fibrosis in the heart after ischemia reperfusion injury. Save
- Ameliorating diabetes-associated atherosclerosis and diabetic nephropathy through modulation of soluble guanylate cyclase. Save
- Cardiovascular characterisation of a novel mouse model that combines hypertension and diabetes co-morbidities. Save
- Selectively targeting the gasdermin-d pore formation to attenuate diabetes associated cardiovascular diseases. Save
- Adverse renal effects of NLRP3 inflammasome inhibition by MCC950 in an interventional model of diabetic kidney disease. Save
- Translational Models of Diabetes Associated Atherosclerosis Save
- Editorial: Translational Approaches for Targeting Cardiovascular Complications of Diabetes. Save
- SOD2 in skeletal muscle: New insights from an inducible deletion model. Save
- Animal models of diabetes-associated vascular diseases: an update on available models and experimental analysis. Save
- Specific NLRP3 Inhibition Protects Against Diabetes-Associated Atherosclerosis Save
- Characterising an Alternative Murine Model of Diabetic Cardiomyopathy. Save
- Serum Amyloid A Stimulates Vascular and Renal Dysfunction in Apolipoprotein E-Deficient Mice Fed a Normal Chow Diet. Save
- Selective Targeting of the NLRP3-inflammasome to attenuate diabetes-associated atherosclerosis. Save
- Selective Targeting of the NLRP3-inflammasome to attenuate diabetes-associated atherosclerosis. Save
- NFκB Inhibition Mitigates Serum Amyloid A-Induced Pro-Atherogenic Responses in Endothelial Cells and Leukocyte Adhesion and Adverse Changes to Endothelium Function in Isolated Aorta. Save
- A novel synthetic small molecule DMFO targets Nrf2 in modulating proinflammatory/antioxidant mediators to ameliorate inflammation. Save
- Recent novel approaches to limit oxidative stress and inflammation in diabetic complications. Save
- Oxidative Stress and NLRP3-Inflammasome Activity as Significant Drivers of Diabetic Cardiovascular Complications: Therapeutic Implications. Save