Pseudostellaria heterophylla polysaccharide mitigates Alzheimer's-like pathology via regulating the microbiota-gut-brain axis in 5 x FAD mice

被引:4
|
作者
He, Chuantong [1 ]
Jiang, Jiahui [1 ]
Liu, Junxin [1 ]
Zhou, Longjian [1 ]
Ge, Yuewei [2 ]
Yang, Zhiyou [1 ,3 ]
机构
[1] Guangdong Ocean Univ, Coll Food Sci & Technol,Zhanjiang Municipal Key La, Guangdong Prov Key Lab Aquat Prod Proc & Safety, Guangdong Prov Engn Lab Marine Biol Prod, Zhanjiang 524088, Peoples R China
[2] Guangdong Pharmaceut Univ, Key Lab Digital Qual Evaluat, Chinese Mat Med State Adm TCM, Guangzhou 510006, Peoples R China
[3] Guangdong Ocean Univ, Coll Food Sci & Technol, Zhanjiang 524088, Peoples R China
关键词
Alzheimer's disease; Pseudostellaria heterophylla polysaccharide; Microbiota-gut-brain axis; Cognitive impairment; DISEASE MOUSE MODEL; ACTIVATION; INFLAMMATION;
D O I
10.1016/j.ijbiomac.2024.132372
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 a progressive neurodegenerative disorder characterised by neuroinflammation, for which gut dysbiosis may be implicated. Our previous study showed that treatment with Pseudostellaria heterophylla aqueous extract and one of its cyclopeptides, heterophyllin B, attenuate memory deficits via immunomodulation and neurite regeneration. However, whether Pseudostellaria heterophylla polysaccharide (PH-PS) exerts neuroprotective effects against AD and its underlying mechanisms remain unclear. The infrared spectrum, molecular weight, and carbohydrate composition of the PH-PS were determined. The results showed that PH-PS (Mw 8.771 kDa) was composed of glucose (57.78 %), galactose (41.52 %), and arabinose (0.70 %). PH-PS treatment ameliorated learning and spatial memory deficits, reduced amyloid beta build-up, and suppressed reactive glia and astrocytes in 5 x FAD mice. 16S rRNA sequencing further showed that PH-PS remodelled the intestinal flora composition by promoting probiotic microbiota, such as Lactobacillus, Muribaculum, Monoglobus, and [Eubacterium]_siraeum_group, and suppressing inflammation-related UCG-009 and Blautia. Additionally, PHPS restored intestinal barrier function; ameliorated peripheral inflammation by reducing the secretion of inflammatory cytokines, thereby converting M1 microglia and A1 astrocyte toward beneficial M2 and A2 phenotypes; and contributed to A beta plaques clearance by upregulation of insulin degradation enzyme and neprilysin. Collectively, our findings demonstrate that PH-PS may prevent the progression of AD via modulation of the gut microbiota and regulation of glial polarisation, which could provide evidence to design a potential diet therapy for preventing or curing AD.
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页数:15
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