Sea-Buckthorn Flavonoids Alleviate High-Fat and High-Fructose Diet-Induced Cognitive Impairment by Inhibiting Insulin Resistance and Neuroinflammation.
Animals
Brain-Derived Neurotrophic Factor
/ genetics
Cognitive Dysfunction
/ drug therapy
Diet, High-Fat
/ adverse effects
Flavonoids
/ administration & dosage
Fructose
/ adverse effects
Hippophae
/ chemistry
Humans
Insulin Receptor Substrate Proteins
/ genetics
Insulin Resistance
Male
Memory
/ drug effects
Mice
Mice, Inbred C57BL
NF-kappa B
/ genetics
Neurons
/ drug effects
cognitive disorders
high-fat and high-fructose diet
neuroinflammation
sea-buckthorn flavonoids
Journal
Journal of agricultural and food chemistry
ISSN: 1520-5118
Titre abrégé: J Agric Food Chem
Pays: United States
ID NLM: 0374755
Informations de publication
Date de publication:
27 May 2020
27 May 2020
Historique:
pubmed:
5
5
2020
medline:
8
1
2021
entrez:
5
5
2020
Statut:
ppublish
Résumé
Sea-buckthorn flavonoids (SFs) have been used as functional food components for their bioactive potential in preventing metabolic complications caused by diet, such as obesity and inflammation. However, the protective effect of SFs on cognitive functions is not fully clear. In this study, a high-fat and high-fructose diet (HFFD)-induced obese mice model was treated with SFs for 14 weeks. It was found that the oral SF administration (0.06% and 0.31% w/w, mixed in diet) significantly reduced bodyweight gain and insulin resistance in the HFFD-fed mice. SFs significantly prevented HFFD-induced neuronal loss and memory impairment in behavioral tests. Additionally, SFs also suppressed the HFFD-induced synaptic dysfunction and neuronal damages by increasing the protein expressions of PSD-95. Furthermore, SF treatment activated the ERK/CREB/BDNF and IRS-1/AKT pathways and inactivated the NF-κB signaling and its downstream inflammatory mediator expressions. In conclusion, SFs are a potential nutraceutical to prevent high-energy density diet-induced cognitive impairments, which could be possibly explained by their mediating effects on insulin signaling and inflammatory responses in the brain.
Identifiants
pubmed: 32363873
doi: 10.1021/acs.jafc.0c00876
doi:
Substances chimiques
Bdnf protein, mouse
0
Brain-Derived Neurotrophic Factor
0
Flavonoids
0
Insulin Receptor Substrate Proteins
0
NF-kappa B
0
Fructose
30237-26-4
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM