Comparative Neuroprotective Effects of Moringa oleifera Seed Oil and Aqueous Extract on Cognitive Functions on a High-Fat, High-Fructose Diet Mice: Focus on Senescence Markers.
Wawaimuli ArozalMuhamad Sadam SafutraAgian Jeffilano BarindaHarri HardiNounik Cheri DwitaHee J LeePublished in: TheScientificWorldJournal (2024)
Several studies have demonstrated that Moringa oleifera (MO) has different pharmacological properties, including neuroprotective effects. However, the role of MO in preventing brain impairment in high-fat, high-fructose diet (HFFD) remains unknown. This study aimed to investigate the neuroprotective effects of MO leaves aqueous extract (MOE) and moringa seed oil (MOO) against brain impairment in mice with HFFD. Twenty-eight male mice were randomly divided into four groups: normal diet, HFFD, HFFD + MOE 500 mg/kgBW, and HFFD + MOO 2 mL/kgBW. Cognitive function was assessed using the Y-maze and novel object recognition (NOR) tests. The p16, p21, and BDNF expressions were analyzed using the RT-PCR method. Senescence-associated beta-galactosidase (SA- β -gal) staining in the brain was also performed. The results showed that administration of MOE or MOO could increase the percentage of alternation and recognition of new objects, prevent the increase of p16 and p21 expression, and ameliorate SA- β -Gal activity in the brain. MOO, but not MOE, increased BDNF expression in senescence brains isolated from HFFD mice. The findings indicate that MOO and MOE possess neuroprotective properties, with MOO demonstrating a greater ability to inhibit the brain senescence process compared to MOE.
Keyphrases
- resting state
- cerebral ischemia
- white matter
- stress induced
- endothelial cells
- dna damage
- functional connectivity
- poor prognosis
- weight loss
- physical activity
- high fat diet induced
- oxidative stress
- type diabetes
- multiple sclerosis
- long non coding rna
- fatty acid
- subarachnoid hemorrhage
- anti inflammatory
- working memory
- insulin resistance
- binding protein