Literature DB >> 35334854

The Effects of Matcha and Decaffeinated Matcha on Learning, Memory and Proteomics of Hippocampus in Senescence-Accelerated (SAMP8) Mice.

Kiharu Igarashi1, Makiko Takagi2, Yoichi Fukushima3.   

Abstract

Although the benefits of the consumption of green tea and its components, including catechins and theanine, regarding aging, memory impairment and age-related cognitive decline have been investigated in senescence-accelerated prone mice (SAMP8), studies that simultaneously measured the kinds of proteins that vary in their expression due to the administration of green tea and its extracts were not found. In this study, the effect of dietary and decaffeinated matcha on protein expression in the hippocampus of SAMP 8 was examined comprehensively, mainly using proteomics. Although improvements in memory and the hair appearance of the back coat were limited upon administering the samples, the following regulations were observed in some of the proteins involved in neuron degeneration, Parkinson's and Alzheimer's diseases, synapse transmission and nerve cell plasticity, antioxidation, glutamate transport and metabolism, GABA (γ-amino butyric acid) formation and transport and excitatory amino acid transporters: proteins downregulated upon sample intake (p < 0.05): brain acid-soluble protein 1, microtubule-associated protein tau, synapsin-2, sodium- and chloride-dependent GABA transporter; proteins that tended to decrease upon sample intake (0.05 < p < 0.10): Parkinson's disease (autosomal recessive and early-onset) 7 and synapsin-1; proteins upregulated upon sample intake (p > 0.95): glutathione S-transferase Mu 1, tubulin alpha-1A chain, dynamin-2, calcium/calmodulin-dependent protein kinase type II subunit gamma and tyrosine 3-monooxygenase/tyrosine 5-monooxygenase activation protein epsilon polypeptide; proteins that tended to increase upon sample intake (0.95 > p > 0.90): glutathione S-transferase Mu7 and soluble carrier family 1 (glial high-affinity glutamate transporter); proteins that tended to decrease: sodium- and chloride-dependent GABA transporter 3. These results indicate that matcha and decaffeinated matcha could reduce aging and cognitive impairment by regulating the expression of these proteins. Furthermore, these proteins could be used as markers for the evaluation of food and its available components for reducing aging and cognitive impairment.

Entities:  

Keywords:  SAMP8; cognitive impairment; decaffeinated matcha; hippocampus protein; matcha green tea; proteomics

Mesh:

Substances:

Year:  2022        PMID: 35334854      PMCID: PMC8952568          DOI: 10.3390/nu14061197

Source DB:  PubMed          Journal:  Nutrients        ISSN: 2072-6643            Impact factor:   5.717


  29 in total

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Journal:  Methods Enzymol       Date:  1999       Impact factor: 1.600

2.  Theanine attenuates memory impairments induced by klotho gene depletion in mice.

Authors:  Bao Trong Nguyen; Naveen Sharma; Eun-Joo Shin; Ji Hoon Jeong; Sung Hoon Lee; Choon-Gon Jang; Seung-Yeol Nah; Toshitaka Nabeshima; Yukio Yoneda; Hyoung-Chun Kim
Journal:  Food Funct       Date:  2019-01-22       Impact factor: 5.396

Review 3.  SAMP8 Mice as a Model of Age-Related Cognition Decline with Underlying Mechanisms in Alzheimer's Disease.

Authors:  Bo Liu; Jie Liu; Jing-Shan Shi
Journal:  J Alzheimers Dis       Date:  2020       Impact factor: 4.472

4.  Japanese carotenoid database with α- and β-carotene, β-cryptoxanthin, lutein, zeaxanthin, lycopene, and fucoxanthin and intake in adult women.

Authors:  Yoichi Fukushima; Chie Taguchi; Yoshimi Kishimoto; Kazuo Kondo
Journal:  Int J Vitam Nutr Res       Date:  2021-05-07       Impact factor: 1.784

5.  Matcha and Its Components Control Angiogenic Potential.

Authors:  Ryota Iwai; Takeshi Ishii; Yoichi Fukushima; Tadashi Okamoto; Masamitsu Ichihashi; Yasuto Sasaki; Ken-Ichi Mizuatni
Journal:  J Nutr Sci Vitaminol (Tokyo)       Date:  2021       Impact factor: 2.000

6.  Long-term green tea catechin administration prevents spatial learning and memory impairment in senescence-accelerated mouse prone-8 mice by decreasing Abeta1-42 oligomers and upregulating synaptic plasticity-related proteins in the hippocampus.

Authors:  Q Li; H F Zhao; Z F Zhang; Z G Liu; X R Pei; J B Wang; Y Li
Journal:  Neuroscience       Date:  2009-07-25       Impact factor: 3.590

7.  Age-related deterioration of ability of acquisition in memory and learning in senescence accelerated mouse: SAM-P/8 as an animal model of disturbances in recent memory.

Authors:  H Yagi; S Katoh; I Akiguchi; T Takeda
Journal:  Brain Res       Date:  1988-11-22       Impact factor: 3.252

8.  Tau protein is required for amyloid {beta}-induced impairment of hippocampal long-term potentiation.

Authors:  Olivia A Shipton; Julie R Leitz; Jenny Dworzak; Christine E J Acton; Elizabeth M Tunbridge; Franziska Denk; Hana N Dawson; Michael P Vitek; Richard Wade-Martins; Ole Paulsen; Mariana Vargas-Caballero
Journal:  J Neurosci       Date:  2011-02-02       Impact factor: 6.167

9.  Green Tea Extracts Attenuate Brain Dysfunction in High-Fat-Diet-Fed SAMP8 Mice.

Authors:  Shintaro Onishi; Shinichi Meguro; Monira Pervin; Hidefumi Kitazawa; Ai Yoto; Mayu Ishino; Yuki Shimba; Yusuke Mochizuki; Shinji Miura; Ichiro Tokimitsu; Keiko Unno
Journal:  Nutrients       Date:  2019-04-11       Impact factor: 5.717

Review 10.  Beneficial Effects of Citrus-Derived Polymethoxylated Flavones for Central Nervous System Disorders.

Authors:  Kentaro Matsuzaki; Yasushi Ohizumi
Journal:  Nutrients       Date:  2021-01-04       Impact factor: 5.717

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