Oleuropein-Rich Olive Leaf Extract Attenuates Neuroinflammation in the Alzheimer's Disease Mouse Model

被引:30
作者
Abdallah, Ihab M. [1 ]
Al-Shami, Kamal M. [1 ]
Yang, Euitaek [1 ]
Wang, Junwei [1 ]
Guillaume, Claudia [2 ]
Kaddoumi, Amal [1 ]
机构
[1] Auburn Univ, Harrison Sch Pharm, Dept Drug Discovery & Dev, Auburn, AL 36849 USA
[2] Modern Olives, Lara, Vic 3212, Australia
关键词
Alzheimer's disease; amyloid-beta; olive leaf extract; oleuropein; neuroinflammation; NLRP3; inflammasome; RAGE; HGMB1; NF-kappa B pathway; NF-KAPPA-B; AMYLOID-BETA CLEARANCE; NLRP3; INFLAMMASOME; MEDITERRANEAN DIET; HYDROPHILIC PHENOLS; TGSWDI MICE; IN-VITRO; BRAIN; OIL; PROTEIN;
D O I
10.1021/acschemneuro.2c00005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) is the most common form of dementia among several neurodegenerative disorders afflicting the elderly. AD is characterized by the deposition of extracellular amyloid-beta (A beta) plaques, disrupted blood-brain barrier (BBB), and neuroinflammation. Several studies have demonstrated the health benefits of olive oil and olive leaf extract (OLE) due to their polyphenolic content. The main phenolic compound in OLE is glycosylated oleuropein (OLG), while the aglycon form of oleuropein (OLA) exists in much lower amounts. This work aimed to evaluate the effect of a low dose of OLG-rich OLE and the mechanism(s) that contributed to the observed beneficial effects against A beta pathology in the homozygous 5xFAD mouse model. Mice were fed with OLE-enriched diet (695 mu g/kg body weight/day) for 3 months, starting at 3 months old. Overall findings demonstrated that OLE reduced neuroinflammation by inhibiting the NF-kappa B pathway and suppressing the activation of NLRP3 inflammasomes and RAGE/HMGB1 pathways. In addition, OLE reduced total A beta brain levels due to increased clearance and reduced production of A beta and enhanced BBB integrity and function, which collectively improved the memory function. Thus, the consumption of OLE as a dietary supplement is expected to stop and/or slow the progression of AD.
引用
收藏
页码:1002 / 1013
页数:12
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