SS-31 / elamipretide is the mitochondrial peptide with arguably the most legitimate clinical development behind it, so I wanted a thread focused just on mechanism rather than hype.
As I understand it, it's a cell-permeable tetrapeptide that concentrates in the inner mitochondrial membrane and associates with cardiolipin. By stabilizing cardiolipin it's thought to preserve cristae structure and improve the efficiency of the electron transport chain, reducing electron leak and ROS rather than just scavenging free radicals downstream. That 'fix the membrane, not mop up radicals' distinction is what makes it mechanistically interesting.
Where I get less certain is the translation. It's been through real trials (primary mitochondrial myopathy, heart failure, dry AMD) with genuinely mixed primary-endpoint results. Can anyone with a closer read summarize where the clinical evidence actually stands versus the cell/animal mechanism? I want to keep those two layers separate.