Selective elimination of amyloid-β-induced senescent neuroblastoma cells by Moringa oleifera leaf extract
- Sci Rep. 2026 May 20. doi: 10.1038/s41598-026-53311-y.
- 1. Faculty of Medicine, Manipal University College Malaysia (MUCM), Jalan Batu Hampar, Bukit Baru, Melaka, 75150, Malaysia.
- 2. Institute of Systems Biology, Universiti Kebangsaan Malaysia, UKM, Bangi, Selangor, 43600, Malaysia.
- 3. Department of Biochemistry, Faculty of Medicine, Manipal University College Malaysia (MUCM), Jalan Batu Hampar, Bukit Baru, Melaka, 75150, Malaysia.
- 4. Faculty of Pharmacy and Health Sciences, Universiti Kuala Lumpur Royal College of Medicine Perak, Jalan Greentown, Ipoh, 30450, Perak, Malaysia. [email protected].
- 5. Department of Biochemistry, Faculty of Medicine, Manipal University College Malaysia (MUCM), Jalan Batu Hampar, Bukit Baru, Melaka, 75150, Malaysia. [email protected].
- 6. Medical Innovation Research Centre (MIRC), Shiga University of Medical Science, Otsu, Shiga, 520-2192, Japan. [email protected].
Accumulation of senescent cells (SnCs) in the ageing brain contributes to Alzheimer's Disease (AD) progression by secreting a senescence-associated secretory phenotype (SASP) that exacerbates neuroinflammation and neurodegeneration. Senolytic agents that selectively eliminate SnCs have emerged as a potential therapeutic strategy; however, safer natural alternatives remain underexplored. In this study, we aimed to investigate the senolytic potential of Moringa oleifera leaf Extract (MOL) in an in vitro AD-senescence model using SH-SY5Y cells exposed to Amyloid-β (Aβ1-42) oligomers. SH-SY5Y cells exposed to 20 µM Aβ oligomers exhibited a senescent phenotype, characterised by increased senescence-associated β-galactosidase (SA-β-gal) positivity and upregulated nuclear expression of p21, p16, and γH2AX. Treatment with 300 µg/mL MOL significantly reduced the number of cells expressing senescence-associated molecular markers and induced Apoptosis in SnCs, while attenuating the secretion of pro-inflammatory SASP cytokines, including IL-8 and TNF-α. Overall findings suggest that MOL Extract preferentially targets SnCs and mitigates SASP-associated inflammation. These results support the potential of MOL as a natural compound with senolytic activity and provide a foundation for further development into its therapeutic relevance in AD.
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