# L-methionine and the L-type Ca2+ channel agonist BAY K 8644 collaboratively contribute to the reduction of depressive-like behavior in mice

**Authors:** Ershu He, Ruixue Ma, Shanglan Qu, Xiaoye Zheng, Xin Peng, Jieyu Ji, Wenhao Ma, Xueyan Zhang, Ying Li, Hanwei Li, Yanjiao Li, Lijuan Li, Zhiting Gong

PMC · DOI: 10.3389/fncir.2024.1435507 · 2024-08-29

## TL;DR

This study shows that combining L-methionine and BAY K 8644 can reduce depression-like behaviors in mice, possibly through DNA methylation and L-type calcium channels.

## Contribution

The study reveals a novel interaction between DNA methylation and L-type Ca2+ channels in modulating depression-like behaviors.

## Key findings

- Reduced Dnmt3a expression was observed in the hippocampal DG region of LPS-induced depression in mice.
- BAY K 8644 partially improved depression-like behaviors but did not increase Dnmt3a expression.
- Combining BAY K 8644 with L-methionine improved depressive-like behaviors more effectively.

## Abstract

The L-type Ca2+ channel (LTCC, also known as Cav1,2) is involved in the regulation of key neuronal functions, such as dendritic information integration, cell survival, and neuronal gene expression. Clinical studies have shown an association between L-type calcium channels and the onset of depression, although the precise mechanisms remain unclear. The development of depression results from a combination of environmental and genetic factors. DNA methylation, a significant epigenetic modification, plays a regulatory role in the pathogenesis of psychiatric disorders such as posttraumatic stress disorder (PTSD), depression, and autism. In our study, we observed reduced Dnmt3a expression levels in the hippocampal DG region of mice with LPS-induced depression compared to control mice. The antidepressant Venlafaxine was able to increase Dnmt3a expression levels. Conversely, Bay K 8644, an agonist of the L-type Ca2+ channel, partially ameliorated depression-like behaviors but did not elevate Dnmt3a expression levels. Furthermore, when we manipulated DNA methylation levels during Bay K 8644 intervention in depression-like models, we found that enhancing the expression of Dnmt3a could improve LPS-induced depression/anxiety-like behaviors, while inhibiting DNA methylation exacerbated anxiety-like behaviors, the combined use of BAY K 8644 and L-methionine can better improve depressive-like behavior. These findings indicate that DNA methylation plays a role in the regulation of depression-like behaviors by the L-type Ca2+ channel, and further research is needed to elucidate the interactions between DNA methylation and L-type Ca2+ channels.

## Linked entities

- **Genes:** DNMT3A (DNA methyltransferase 3 alpha) [NCBI Gene 1788]
- **Chemicals:** L-methionine (PubChem CID 6137), BAY K 8644 (PubChem CID 2303), Venlafaxine (PubChem CID 5656)
- **Diseases:** depression (MONDO:0002050), posttraumatic stress disorder (MONDO:0005146), autism (MONDO:0005260)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** CACNA1C (calcium voltage-gated channel subunit alpha1 C) [NCBI Gene 775] {aka CACH2, CACN2, CACNA1C-IT2, CACNL1A1, CCHL1A1, CaV1.2}, DNMT3A (DNA methyltransferase 3 alpha) [NCBI Gene 1788] {aka DNMT3A2, HESJAS, M.HsaIIIA, TBRS}
- **Diseases:** autism (MESH:D001321), psychiatric disorders (MESH:D001523), anxiety (MESH:D001007), PTSD (MESH:D013313), depression (MESH:D003866)
- **Chemicals:** LPS (MESH:D008070), Venlafaxine (MESH:D000069470), BAY K 8644 (MESH:D001498), L-methionine (MESH:D008715)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11391425/full.md

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Source: https://tomesphere.com/paper/PMC11391425