Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Apr 14;14(8):2667.
doi: 10.3390/jcm14082667.

Healing with Love: Oxytocin Accelerates Oral Ulcer Recovery by Reducing Inflammation

Affiliations

Healing with Love: Oxytocin Accelerates Oral Ulcer Recovery by Reducing Inflammation

Mert Zeytinoğlu et al. J Clin Med. .

Abstract

Background: Oral ulcerative mucositis (OUM) is a painful, inflammatory mucosa lesion that impairs quality of life. Despite available treatments, effective agents that promote faster healing and modulate inflammation are still needed. Oxytocin (OT), a neuropeptide with anti-inflammatory and antioxidant properties, may aid wound healing by regulating the remodeling of the extracellular matrix (ECM). This study investigates the effects of OT on oral ulcer healing in rats, focusing on its modulation of the MMP-2/TIMP-2 pathway. Methods: Acetic acid 70% was used as the oral mucosal ulcer inducer. Thirty-six Wistar albino rats were divided into control, oral ulcer + saline, and oral ulcer + OT (intraperitoneally for 15 days) groups. Histopathological, biochemical, and molecular analyses were performed. Buccal mucosa tissue was examined for TNF-α, TIMP-2, and MMP-2 levels via ELISA, while oxidative stress markers and pentraxin-3 (PTX3) were also assessed. Results: OT significantly preserved epithelial integrity and reduced fibrosis compared to the saline group (p < 0.001). TNF-α, MMP-2, PTX3, and malondialdehyde levels were significantly lower, while TIMP-2 levels were elevated in the OT-treated group (p < 0.01). Histopathological analysis confirmed reduced inflammation and enhanced tissue organization. Conclusions: OT accelerates oral ulcer healing by modulating inflammation, oxidative stress, and ECM remodeling via the MMP-2/TIMP-2 pathway. These findings highlight its potential as a therapeutic agent for managing mucosal injuries. Further clinical studies are warranted.

Keywords: MMP-2/TIMP-2 pathway; inflammation; oral ulcerative mucositis; oxidative stress; oxytocin.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Histopathological findings × 20 and 40 magnification, hematoxylin, and eosine stain. (A,B) Normal control group buccal mucosa, normal epithelium (line); (C,D) oral ulcer and % 0.9 NaCl given group buccal mucosa, disrupted epithelium (arrow), and fibrosis (f); (E,F) oral ulcer and OT given group buccal mucosa, healed epithelium (line), and connective tissue (ct).

Similar articles

Cited by

  • Oxytocin, Vasopressin and Stress: A Hormetic Perspective.
    Nazarloo HP, Kingsbury MA, Lamont H, Dale CV, Nazarloo P, Davis JM, Porges EC, Cuffe SP, Carter CS. Nazarloo HP, et al. Curr Issues Mol Biol. 2025 Aug 7;47(8):632. doi: 10.3390/cimb47080632. Curr Issues Mol Biol. 2025. PMID: 40864786 Free PMC article. Review.

References

    1. Sonis S.T., Villa A. Phase II investigational oral drugs for the treatment of radio/chemotherapy induced oral mucositis. Expert. Opin. Investig. Drugs. 2018;27:147–154. doi: 10.1080/13543784.2018.1427732. - DOI - PubMed
    1. Cinausero M., Aprile G., Ermacora P., Basile D., Vitale M.G., Fanotto V., Parisi G., Calvetti L., Sonis S.T. New frontiers in the pathobiology and treatment of cancer regimen-related mucosal injury. Front. Pharmacol. 2017;8:354. doi: 10.3389/fphar.2017.00354. - DOI - PMC - PubMed
    1. Arafat E., El-Khair S., Elsamanoudy A., Shabaan D. Study of the Possible Alleviated Role of Atorvastatin on Irinotecan-Induced Lingual Mucosal Damage: Histological and Molecular Study. Oxidative Med. Cell. Longev. 2021;2021:1–13. doi: 10.1155/2021/9690047. - DOI - PMC - PubMed
    1. Da Costa Cunha Mafra C., Vasconcelos R., De Medeiros C., Leitão R., Brito G., Costa D., Guerra G., De Araújo R., Medeiros A., De Araújo A. Gliclazide Prevents 5-FU-Induced Oral Mucositis by Reducing Oxidative Stress, Inflammation, and P-Selectin Adhesion Molecules. Front. Physiol. 2019;10:327. doi: 10.3389/fphys.2019.00327. - DOI - PMC - PubMed
    1. Haagen J., Krohn H., Röllig S., Schmidt M., Wolfram K., Dörr W. Effect of selective inhibitors of inflammation on oral mucositis: Preclinical studies. Radiother. Oncol. J. Eur. Soc. Ther. Radiol. Oncol. 2009;92:472–476. doi: 10.1016/j.radonc.2009.06.006. - DOI - PubMed

LinkOut - more resources