4.7 Article

Theanine, a Tea-Leaf-Specific Amino Acid, Alleviates Stress through Modulation of Npas4 Expression in Group-Housed Older Mice

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MDPI
DOI: 10.3390/ijms24043983

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DNA methyltransferase; glucocorticoid receptor; group housing; IL-1 beta; Npas4; REST; stress; theanine

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Group-housed older mice show increased adrenal hypertrophy, a marker of stress, but theanine can suppress stress. In group-reared older mice, the expression of REST, a gene repressor, was increased while the expression of Npas4, involved in brain regulation, was lower. Theanine reduced stress response and tended to increase Npas4 expression, suggesting that theanine avoids the decrease in Npas4 expression by suppressing its transcriptional repressors.
Group rearing is a common housing condition, but group-housed older mice show increased adrenal hypertrophy, a marker of stress. However, the ingestion of theanine, an amino acid unique to tea leaves, suppressed stress. We aimed to elucidate the mechanism of theanine's stress-reducing effects using group-reared older mice. The expression of repressor element 1 silencing transcription factor (REST), which represses excitability-related genes, was increased in the hippocampus of group-reared older mice, whereas the expression of neuronal PAS domain protein 4 (Npas4), which is involved in the regulation of excitation and inhibition in the brain, was lower in the hippocampus of older group-reared mice than in same-aged two-to-a-house mice. That is, the expression patterns of REST and Npas4 were found to be just inversely correlated. On the other hand, the expression levels of the glucocorticoid receptor and DNA methyltransferase, which suppress Npas4 transcription, were higher in the older group-housed mice. In mice fed theanine, the stress response was reduced and Npas4 expression tended to be increased. These results suggest that Npas4 expression was suppressed by the increased expression of REST and Npas4 downregulators in the group-fed older mice, but that theanine avoids the decrease in Npas4 expression by suppressing the expression of Npas4 transcriptional repressors.

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