The role and mechanisms of N,N-dimethylglycine sodium in promoting wound healing in mice.
10.7507/1001-5515.202411042
- Author:
Shuchang GUO
1
;
Zhenyang ZHANG
1
;
Baoying QI
1
;
Yuxiao ZHOU
1
;
Meng LI
1
;
Tianzhu LIANG
1
;
Huan YAN
1
;
Qiuyu WANG
1
;
Lili JIN
1
Author Information
1. School of Life Sciences, Liaoning University, Shenyang 110036, P. R. China.
- Publication Type:Journal Article
- Keywords:
Immune-inflammatory microenvironment;
Keratinocytes;
N,N-dimethylglycine sodium;
Wound healing
- MeSH:
Animals;
Wound Healing/drug effects*;
Mice;
Cell Proliferation/drug effects*;
Keratinocytes/drug effects*;
Cell Movement/drug effects*;
Cell Differentiation/drug effects*;
Glycine/pharmacology*;
Skin/injuries*;
Male
- From:
Journal of Biomedical Engineering
2025;42(4):824-831
- CountryChina
- Language:Chinese
-
Abstract:
N,N-Dimethylglycine (DMG) is a glycine derivative, and its sodium salt (DMG-Na) has been demonstrated to possess various biological activities, including immunomodulation, free radical scavenging, and antioxidation, collectively contributing to the stability of tissue and cellular functions. However, its direct effects and underlying mechanisms in wound healing remain unclear. In this study, a full-thickness excisional wound model was established on the dorsal skin of mice, and wounds were treated locally with DMG-Na. Wound healing progression was assessed by calculating wound closure rates. Histopathological analysis was conducted using hematoxylin-eosin (HE) staining, and keratinocyte proliferation, migration, and differentiation were evaluated using CCK-8 assays, scratch wound assays, and quantitative reverse transcription PCR (qRT-PCR). Inflammation-related cytokine expression in keratinocytes was analyzed via ELISA and qRT-PCR. Results revealed that DMG-Na treatment significantly accelerated wound healing in mice and improved overall wound closure quality. The wound healing rates on days 3, 6, and 9 were 49.18%, 68.87%, and 90.55%, respectively, with statistically significant differences compared to the control group ( P<0.05). DMG-Na treatment downregulated the mRNA levels of keratinocyte differentiation markers while enhancing cell proliferation and migration ( P<0.05). Furthermore, DMG-Na decreased the secretion of LPS-induced keratinocyte inflammatory cytokines, including IL-1β, IL-6, IL-8, TNF-α, and CXCL10 ( P<0.05). These findings indicate that DMG-Na regulates inflammatory responses and promotes keratinocyte proliferation and migration, thereby facilitating the healing of skin wounds.
