Vitamin B complex blocks the dust fall PM2.5‐induced acute lung injury through DNA methylation in rats
This study aimed to explore whether vitamin B complex (folic acid, B6, and B12) could avert DNA methylation changes associated with inflammation induced by acute PM2.5 exposure. Sprague‐Dawley rats were administered by gavage with different concentrations of vitamin B complex once a day for 28 days,...
Gespeichert in:
Veröffentlicht in: | Environmental toxicology 2023-02, Vol.38 (2), p.403-414 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | This study aimed to explore whether vitamin B complex (folic acid, B6, and B12) could avert DNA methylation changes associated with inflammation induced by acute PM2.5 exposure. Sprague‐Dawley rats were administered by gavage with different concentrations of vitamin B complex once a day for 28 days, and then by intratracheal instillation with saline or PM2.5 once every 2 days for three times. Vitamin B continued to be taken during the PM2.5 exposure. Rats were sacrificed 24 h after the last exposure. The results showed that vitamin B complex could block the pathological changes and injury in lungs induced by PM2.5. Meanwhile, vitamin B complex could prevent the abnormal DNA methylation of IL‐4 and IFN‐γ to antagonize the imbalance of IL‐4/IFN‐γ associated with inflammation. It was further found that vitamin B complex could regulate DNA methyltransferases (DNMTs) and increase the S‐adenosylmethionine (SAM)/S‐Adenosyl‐L‐homocysteine (SAH) ratio to reverse the hypomethylation of genomic DNA and the abnormal DNA methylation of IL‐4 and IFN‐γ. In conclusion, vitamin B complex has a protective effect on acute lung injury by attenuating abnormal DNA methylation induced by PM2.5 in rats. This study may provide a new insight into the physiological function of vitamin B to prevent the health effects induced by PM2.5. |
---|---|
ISSN: | 1520-4081 1522-7278 |
DOI: | 10.1002/tox.23689 |