Abstract

DNA methylation is one of the essential factors in the control of gene expression. Folic acid, methionine and choline (methyl donors)–all nutrients related to one-carbon metabolism–are known as important mediators of DNA methylation. A previous study has shown that long-term administration of a diet lacking in methyl donors caused global DNA hypermethylation in the brain (Pogribny et al., 2008). However, no study has investigated the effects of a diet lacking in methyl donors during the developmental period on emotional behaviors such as fear and anxiety-like behavior in association with gene expressions in the brain. In addition, it has not been elucidated whether a diet supplemented with methyl donors later in life can reverse these changes. Therefore, we examined the effects of methyl donor deficiency during the developmental period on fear memory acquisition/extinction and anxiety-like behavior, and the relevant gene expressions in the hippocampus in juvenile (6-wk) and adult (12-wk) mice. We found that juvenile mice fed a methyl-donor-deficient diet had impaired fear memory acquisition along with decreases in the gene expressions of Dnmt3a and Dnmt3b. In addition, reduced anxiety-like behavior with decreased gene expressions of Grin2b and Gabar2 was observed in both the methyl-donor-deficient group and the body-weight-matched food-restriction group. After being fed a diet supplemented with methyl donors ad libitum, adult mice reversed the alteration of gene expression of Dnmt3a, Dnmt3b, Grin2b and Gabar2, but anxiety-like behavior became elevated. In addition, impaired fear-memory formation was observed in the adult mice fed the methyl-donor-deficient diet during the developmental period. Our study suggested that developmental alterations in the one-carbon metabolic pathway in the brain could have effects on emotional behavior and memory formation that last into adulthood.

Highlights

  • Many mental disorders including anxiety disorders such as specific phobia, panic disorder, post-traumatic disorder (PTSD) and mood disorders develop in early life stages [1,2,3]; the age of onset of anxiety disorders is earlier than those of other disorders [4]

  • Post hoc comparison indicated that the body weights of the folate-methionine-choline deficient (FMCD) group at 4–12 weeks of age were significantly reduced compared to the control group (p,0.001), and the body weights in the food restriction (FR) group at 4–8 weeks were significantly reduced compared to the control group (p,0.05)

  • Restriction of food intake from 3 to 6 weeks induced the delayed acquisition of hippocampus-dependent fear memory, but this change was reversed by feeding of the normal diet ad libitum for the subsequent 6 weeks

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Summary

Introduction

Many mental disorders including anxiety disorders such as specific phobia, panic disorder, post-traumatic disorder (PTSD) and mood disorders develop in early life stages [1,2,3]; the age of onset of anxiety disorders is earlier than those of other disorders [4]. There are notable individual differences in vulnerability, resilience and treatment response. The Tokyo subway sarin attack in 1995 by a radical cult produced severe PTSD in some bystanders, but not to others. Gray-matter volume reductions in the left anterior cingulate cortex were observed only in the victims who developed PTSD [5]. Individual factors play roles in the pathogenesis, development, and treatment response of mental disorders

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