The Lacto-Tetrapeptide Gly-Thr-Trp-Tyr, β-Lactolin, Improves Spatial Memory Functions via Dopamine Release and D1 Receptor Activation in the Hippocampus.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
15 Oct 2019
Historique:
received: 25 08 2019
revised: 11 10 2019
accepted: 11 10 2019
entrez: 18 10 2019
pubmed: 18 10 2019
medline: 26 3 2020
Statut: epublish

Résumé

Peptides containing tryptophan-tyrosine sequences, including the lacto-tetrapeptide glycine-threonine-tryptophan-tyrosine (GTWY) and β-lactolin, from β-lactoglobulin in whey enzymatic digestion, enhance hippocampus-dependent memory functions, which are blocked by the systemic administration of dopamine D1-like antagonist. In this study, we investigated the role of the hippocampal dopaminergic system in the memory-enhancing effect of β-lactolin. The results of in vivo microdialysis revealed that oral administration of β-lactolin increased the extracellular concentration of dopamine in the hippocampus and enhanced both spatial working memory, as measured in the Y-maze test, and spatial reference memory, as measured in the novel object location test. These memory-enhancing effects of β-lactolin, but not the baseline memory functions, were impaired by the knockdown of the dopamine D1 receptor subtype in the hippocampus. β-Lactolin also enhanced object memory, as measured by the novel object recognition test. However, D1 knockdown in the hippocampus spared this memory function either with or without the administration of β-lactolin. The present results indicate that oral administration of β-lactolin increases dopamine release and D1 receptor signaling in the hippocampus, thereby enhancing spatial memory, but it may improve object memory via a separate mechanism.

Identifiants

pubmed: 31618902
pii: nu11102469
doi: 10.3390/nu11102469
pmc: PMC6835598
pii:
doi:

Substances chimiques

Dopamine Agonists 0
Drd1 protein, mouse 0
Nootropic Agents 0
Oligopeptides 0
Receptors, Dopamine D1 0
Dopamine VTD58H1Z2X

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Core Research for Evolutional Science and Technology
ID : JP18gm0910012
Organisme : Japan Society for the Promotion of Science
ID : 16H05132
Organisme : Japan Society for the Promotion of Science
ID : 17K19457
Organisme : Japan Society for the Promotion of Science
ID : 17K08593
Organisme : Ministry of Education, Culture, Sports, Science and Technology in Japan
ID : 18H05429

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Auteurs

Tatsuhiro Ayabe (T)

Research Laboratories for Health Science & Food Technologies, Kirin Holdings Company Ltd., 1-13-5 Fukuura Kanazawa-ku, Yokohama-shi, Kanagawa 236-0004, Japan. Tatsuhiro_Ayabe@kirin.co.jp.

Yasuhisa Ano (Y)

Research Laboratories for Health Science & Food Technologies, Kirin Holdings Company Ltd., 1-13-5 Fukuura Kanazawa-ku, Yokohama-shi, Kanagawa 236-0004, Japan. Yasuhisa_Ano@kirin.co.jp.

Rena Ohya (R)

Research Laboratories for Health Science & Food Technologies, Kirin Holdings Company Ltd., 1-13-5 Fukuura Kanazawa-ku, Yokohama-shi, Kanagawa 236-0004, Japan. Rena_Ohya@kirin.co.jp.

Shiho Kitaoka (S)

Division of Pharmacology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan. skitaoka@med.kobe-u.ac.jp.
AMED-CREST, Chiyoda-ku, Tokyo 100-0004, Japan. skitaoka@med.kobe-u.ac.jp.

Tomoyuki Furuyashiki (T)

Division of Pharmacology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan. tfuruya@med.kobe-u.ac.jp.
AMED-CREST, Chiyoda-ku, Tokyo 100-0004, Japan. tfuruya@med.kobe-u.ac.jp.

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Classifications MeSH