To evaluate the effects of ethanolic extracts from Rosmarinus officinalis, Cynara cardunculus, and Myrtus communis on mitochondrial damage induced by oxidized LDL in endothelial cells.
Approach:
Cell Viability and Proliferation Assessment: MTT assay and acridine orange staining were used to evaluate cell viability and proliferation under therapeutic-equivalent concentrations.
Mitochondrial Membrane Potential Measurement: Rhodamine 6G was utilized to assess mitochondrial membrane potential (Δψm) in treated cells.
Gene Expression Analysis: RT-qPCR analyzed the expression of genes related to mitochondrial dynamics, mitophagy, and antioxidant defense in response to treatment.
Key Findings:
All extracts preserved mitochondrial membrane potential and architecture in healthy HUVECs in a dose-dependent manner.
In the ox-LDL model, extracts downregulated pro-fission genes (DRP1, FIS1, MFF) and upregulated fusion genes (MFN2, OPA1).
C. cardunculus significantly upregulated PINK1 and PARKIN, enhancing mitophagy.
R. officinalis and M. communis increased FUNDC1 and OPTN, indicating receptor-mediated clearance pathways.