S-9-PAHSA can reduce neuronal apoptosis by promoting mitochondrial
autophagy in 5xFAD mice
Abstract
Alzheimer’s disease (AD) is a prevalent neurodegenerative disorder
characterized by significant cognitive impairment and predominantly
affects the elderly. With no effective cure available, research
continues to explore novel therapeutic and preventive strategies.
Palmitic acid-9-hydroxystearic acid (9-PAHSA), a novel class of
bioactive lipids with anti-inflammatory and anti-diabetic properties,
has shown potential as a dietary supplement. Mitochondrial dysfunction
is recognized as a significant pathological feature of AD, with impaired
mitophagy leading to the accumulation of dysfunctional mitochondria,
thus exacerbating disease progression. This study evaluates the
hypothesis that S-9-PAHSA can ameliorate cognitive dysfunction in AD by
enhancing mitochondrial autophagy in 5xFAD mice. The treatment group
received S-9-PAHSA in their drinking water for three months. Behavioral
studies were conducted using the Morris Water Maze (MWM) and Y-Maze,
with further assessments of amyloid-beta (Aβ) plaque deposition,
neuronal apoptosis, and mitochondrial health. S-9-PAHSA significantly
enhanced spatial learning and memory, reduced amyloid plaque deposition,
decreased neuronal apoptosis, and improved mitochondrial health and
autophagy in 5xFAD mice. These findings suggest that S-9-PAHSA holds
promise as a supplementary preventive and therapeutic strategy for
Alzheimer’s disease treatment.