Natural antioxidant formula ameliorates lipopolysaccharide-induced impairment of hippocampal neurogenesis and contextual fear memory through suppression of neuroinflammation in rats

被引:3
|
作者
Zeng, Wen [1 ]
Takashima, Kazumi [1 ,2 ]
Tang, Qian [1 ,2 ]
Zou, Xinyu [1 ,2 ]
Ojiro, Ryota [1 ,2 ]
Ozawa, Shunsuke [1 ,2 ]
Jin, Meilan [3 ]
Ando, Yujiro [4 ]
Yoshida, Toshinori [1 ,2 ]
Shibutani, Makoto [1 ,2 ,5 ,6 ]
机构
[1] Tokyo Univ Agr & Technol, Lab Vet Pathol, 3-5-8 Saiwai Cho, Fuchu, Tokyo 1838509, Japan
[2] Tokyo Univ Agr & Technol, Grad Sch Agr, Cooperat Div Vet Sci, 3-5-8 Saiwai Cho, Fuchu, Tokyo 1838509, Japan
[3] Southwest Univ, Coll Vet Med, Lab Vet Pathol, 2 Tiansheng Rd, Chongqing 400715, Peoples R China
[4] Withpety Co Ltd, 1-9-3 Shin Ishikawa,Aoba Ku, Yokohama, Kanagawa 2250003, Japan
[5] Tokyo Univ Agr & Technol, Inst Global Innovat Res, 3-5-8 Saiwai Cho, Fuchu, Tokyo 1838509, Japan
[6] Tokyo Univ Agr & Technol, Inst Agr, Div Anim Life Sci, Lab Vet Pathol, 3-5-8 Saiwai Cho, Fuchu, Tokyo 1838509, Japan
关键词
Natural antioxidants; Contextual fear memory; Hippocampal neurogenesis; Lipopolysaccharide (LPS); Neuroinflammation; Rat; GINKGO-BILOBA EXTRACT; FERULIC ACID; COGNITIVE IMPAIRMENT; NITROSATIVE STRESS; EXPRESSION; GENE; ALPHA; MODEL; NMDA; INFLAMMATION;
D O I
10.1016/j.jchemneu.2023.102285
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
This study investigated the ameliorating effects of a natural antioxidant formula (NAF) consisting of Ginkgo biloba leaf extract, docosahexaenoic acid/eicosapentaenoic acid, ferulic acid, flaxseed oil, vitamin E, and vitamin B12 on a lipopolysaccharide (LPS)-induced cognitive dysfunction model in rats. Six-week-old rats received a diet containing 0.5% (w/w) NAF for 38 days from Day 1, and LPS (1 mg/kg body weight) was administered intraperitoneally once daily on Days 8 and 10. On Day 11, LPS alone increased interleukin-1 beta and tumor necrosis factor-alpha in the hippocampus and cerebral cortex and the numbers of M1-type microglia/macrophages and GFAP+ reactive astrocytes in the hilus of the hippocampal dentate gyrus. NAF treatment decreased brain proinflammatory cytokine levels and increased the number of M2-type microglia/macrophages. During Days 34-38, LPS alone impaired fear memory acquisition and the extinction learning process, and NAF facilitated fear extinction learning. On Day 38, LPS alone decreased the number of type-3 neural progenitor cells in the hippocampal neurogenic niche, and NAF restored the number of type-3 neural progenitor cells and increased the numbers of both immature granule cells in the neurogenic niche and reelin+ hilar interneurons. Thus, NAF exhibited antiinflammatory effects and ameliorated LPS-induced adverse effects on hippocampal neurogenesis and fear memory learning, possibly through amplification of reelin signaling by hilar interneurons. These results suggest that neuroinflammation is a key factor in the development of LPS-induced impairment of fear memory learning, and supplementation with NAF in the present study helped to prevent hippocampal neurogenesis and disruptive neurobehaviors caused by neuroinflammation.
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页数:17
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