Effects of low-level laser irradiation on canine fibroblasts.

Autor: Purba MS; Joint Graduate School of Veterinary Medicine, Yamaguchi University.; Laboratory of Veterinary Surgery, Joint Faculty of Veterinary Medicine, Yamaguchi University., Anggoro D; Joint Graduate School of Veterinary Medicine, Yamaguchi University.; Laboratory of Veterinary Surgery, Joint Faculty of Veterinary Medicine, Yamaguchi University., Itoh H; Laboratory of Small Animal Clinical Science, Joint Faculty of Veterinary Medicine, Yamaguchi University., Itamoto K; Laboratory of Small Animal Clinical Science, Joint Faculty of Veterinary Medicine, Yamaguchi University., Nemoto Y; Laboratory of Veterinary Radiology, Joint Faculty of Veterinary Medicine, Yamaguchi University., Nakaichi M; Laboratory of Veterinary Radiology, Joint Faculty of Veterinary Medicine, Yamaguchi University., Sunahara H; Laboratory of Veterinary Surgery, Joint Faculty of Veterinary Medicine, Yamaguchi University., Tani K; Laboratory of Veterinary Surgery, Joint Faculty of Veterinary Medicine, Yamaguchi University.
Jazyk: angličtina
Zdroj: The Journal of veterinary medical science [J Vet Med Sci] 2024 Nov 13. Date of Electronic Publication: 2024 Nov 13.
DOI: 10.1292/jvms.24-0318
Abstrakt: Low-level laser (LLL) therapy is a well-known noninvasive treatment that stimulates fibroblasts to improve wound healing. LLL can improve fibroblast proliferation and migration without causing toxicity. The present study aimed to evaluate the effects of two laser wavelengths at different irradiation times on canine fibroblasts. Fibroblasts were isolated from canine oral mucosa. After seeding for 24 hr, the fibroblasts were irradiated using the Erchonia ®️ EVL dual-diode laser at wavelengths of 405 nm (5 mW) and 640 nm (7.5 mW) with irradiation times of 120, 360, and 1,800 sec. The proliferating and viability cells were evaluated 24 hr after laser irradiation. Wound closure rates were calculated at 0, 24, and 48 hr after laser irradiation. Parameters, including proliferation cell, cell viability, and cell migration, tended to be higher in the 360-sec group (405 nm) and 120-sec group (640 nm) than in other groups. Our findings suggest that LLL therapy at wavelengths of 405 and 640 nm with an irradiation time of 120-360 sec (0.26-0.51 J/cm 2 ) can stimulate the proliferation and migration of canine fibroblasts. This finding may contribute to a better understanding of the beneficial role of LLL stimulation in canine wound healing.
Databáze: MEDLINE