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S-9-PAHSA can reduce neuronal apoptosis by promoting mitochondrial autophagy in 5xFAD mice
  • Chenyu Lu
Chenyu Lu
Fudan University

Corresponding Author:22211520025@m.fudan.edu.cn

Author Profile

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.
16 Oct 2024Submitted to European Journal of Neuroscience
19 Oct 2024Submission Checks Completed
19 Oct 2024Assigned to Editor
21 Oct 2024Review(s) Completed, Editorial Evaluation Pending
27 Oct 2024Reviewer(s) Assigned
07 Dec 2024Editorial Decision: Revise Major