posted on 2025-11-18, 13:38authored byAlex Malik Parker
Mitochondria are critical energy-generating organelles that power the heart to pump blood around the body. Mitochondrial dysregulation in the heart is a key pathological mechanism observed in individuals with type 2 diabetes (T2D), which can lead to heart failure. This thesis investigated several mitochondrial-targeted therapies, AP39, SKQ1 and SS31, to treat T2D-induced cardiac dysfunction. SS31, known for protecting the structural integrity of the mitochondria, was able to restore mitochondrial regulation and improve cardiac function in preclinical models of T2D. Findings from this study may facilitate the clinical progression of mitochondrial-targeted therapeutics and treatment options for individuals with T2D cardiac dysfunction.<p></p>
History
Campus location
Australia
Principal supervisor
Rebecca Ritchie
Additional supervisor 1
Miles De Blasio
Additional supervisor 2
Max (Shiang) Lim
Additional supervisor 3
Jarmon Lees
Year of Award
2025
Department, School or Centre
Drug Discovery Biology
Additional Institution or Organisation
Monash Institute of Pharmaceutical Sciences
Course
Doctor of Philosophy
Degree Type
DOCTORATE
Faculty
Faculty of Pharmacy and Pharmaceutical Sciences
Rights Statement
The author retains copyright of this thesis. It must only be used for personal non-commercial research, education and study. It must not be used for any other purposes and may not be transmitted or shared with others without prior permission. For further terms use the In Copyright link under the License field.