Caffeic acid reduces oxidative stress and microglial activation in the mouse hippocampus.


Journal

Tissue & cell
ISSN: 1532-3072
Titre abrégé: Tissue Cell
Pays: Scotland
ID NLM: 0214745

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 28 02 2019
revised: 19 07 2019
accepted: 21 07 2019
entrez: 5 10 2019
pubmed: 5 10 2019
medline: 12 2 2020
Statut: ppublish

Résumé

A number of studies have indicated the benefits of coffee consumption on physical and mental health; however, scientific evidence on these effects, in particular of the benefits to brain function, has not been determined. In the present study, we aimed to determine the benefits of caffeic acid in the nervous system. For this purpose, we administered doses of 0 or 300 mg/kg for 30 days to mice that were not otherwise affected. We analyzed survival of newly born cells, oxidative stress, inflammatory marker expression, and microglial activation in the hippocampus. We found that caffeic acid had no effect on the expression levels of neurotrophic factors and inflammatory or anti-inflammatory cytokines. However, caffeic acid-treated mice exhibited significantly lower levels of 4-hydroxynonenal, an oxidative stress marker, in the hippocampus, as well as significantly fewer activated microglia. Abnormally high oxidative stress, as well as activated microglia accumulation are both considered to relate to the pathophysiology of neurological and psychiatric disorders. The present study demonstrates the physiological effects of caffeic acid and may explain the suggested benefits of coffee consumption on brain health.

Identifiants

pubmed: 31582013
pii: S0040-8166(19)30084-9
doi: 10.1016/j.tice.2019.07.006
pii:
doi:

Substances chimiques

Antioxidants 0
Caffeic Acids 0
caffeic acid U2S3A33KVM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

14-20

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Minori Koga (M)

Department of Psychiatry, Graduate School of Medicine, Hokkaido University, Kita 15, Nishi 7, Sapporo Hokkaido, 060-8638, Japan. Electronic address: mkoga3@ndmc.ac.jp.

Shin Nakagawa (S)

Department of Psychiatry, Graduate School of Medicine, Hokkaido University, Kita 15, Nishi 7, Sapporo Hokkaido, 060-8638, Japan.

Akiko Kato (A)

Department of Psychiatry, Graduate School of Medicine, Hokkaido University, Kita 15, Nishi 7, Sapporo Hokkaido, 060-8638, Japan.

Ichiro Kusumi (I)

Department of Psychiatry, Graduate School of Medicine, Hokkaido University, Kita 15, Nishi 7, Sapporo Hokkaido, 060-8638, Japan.

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Classifications MeSH