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Bifidobacteria-Fermented Red Ginseng and Its Constituents Ginsenoside Rd and Protopanaxatriol Alleviate Anxiety/Depression in Mice by the Amelioration of Gut Dysbiosis.
Han, Sang-Kap; Joo, Min-Kyung; Kim, Jeon-Kyung; Jeung, Woonhee; Kang, Heerim; Kim, Dong-Hyun.
Afiliação
  • Han SK; Neurobiota Research Center, College of Pharmacy, Kyung Hee University, Seoul 02447, Korea.
  • Joo MK; Neurobiota Research Center, College of Pharmacy, Kyung Hee University, Seoul 02447, Korea.
  • Kim JK; Neurobiota Research Center, College of Pharmacy, Kyung Hee University, Seoul 02447, Korea.
  • Jeung W; R&BD Center, Korea Yakult Co. Ltd., Yongin 17086, Korea.
  • Kang H; R&BD Center, Korea Yakult Co. Ltd., Yongin 17086, Korea.
  • Kim DH; Neurobiota Research Center, College of Pharmacy, Kyung Hee University, Seoul 02447, Korea.
Nutrients ; 12(4)2020 Mar 26.
Article em En | MEDLINE | ID: mdl-32224881
ABSTRACT
Gut dysbiosis is closely connected with the outbreak of psychiatric disorders with colitis. Bifidobacteria-fermented red ginseng (fRG) increases the absorption of ginsenoside Rd and protopanxatriol into the blood in volunteers and mice. fRG and Rd alleviates 2,4,6-trinitrobenzenesulfonic acid-induced colitis in mice. Therefore, to understand the gut microbiota-mediated mechanism of fRG against anxiety/depression, we examined the effects of red ginseng (RG), fRG, ginsenoside Rd, and protopanaxatriol on the occurrence of anxiety/depression, colitis, and gut dysbiosis in mice. Mice with anxiety/depression were prepared by being exposed to two stressors, immobilization stress (IS) or Escherichia coli (EC). Treatment with RG and fRG significantly mitigated the stress-induced anxiety/depression-like behaviors in elevated plus maze, light-dark transition, forced swimming (FST), and tail suspension tasks (TST) and reduced corticosterone levels in the blood. Their treatments also suppressed the stress-induced NF-κB activation and NF-κB+/Iba1+ cell population in the hippocampus, while the brain-derived neurotrophic factor (BDNF) expression and BDNF+/NeuN+ cell population were increased. Furthermore, treatment with RG or fRG suppressed the stress-induced colitis they suppressed myeloperoxidase activity, NF-κB activation, and NF-κB+/CD11c+ cell population in the colon. In particular, fRG suppressed the EC-induced depression-like behaviors in FST and TST and colitis more strongly than RG. fRG treatment also significantly alleviated the EC-induced NF-κB+/Iba1+ cell population and EC-suppressed BDNF+/NeuN+ cell population in the hippocampus more strongly than RG. RG and fRG alleviated EC-induced gut dysbiosis they increased Bacteroidetes population and decreased Proteobacteria population. Rd and protopanaxatriol also alleviated EC-induced anxiety/depression and colitis. In conclusion, fRG and its constituents Rd and protopanaxatriol mitigated anxiety/depression and colitis by regulating NF-κB-mediated BDNF expression and gut dysbiosis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sapogeninas / Ginsenosídeos / Depressão / Microbioma Gastrointestinal / Alimentos Fermentados Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Nutrients Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sapogeninas / Ginsenosídeos / Depressão / Microbioma Gastrointestinal / Alimentos Fermentados Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Nutrients Ano de publicação: 2020 Tipo de documento: Article