Effects of low-level laser irradiation on canine fibroblasts
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...
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Veröffentlicht in: | Journal of Veterinary Medical Science 2024, pp.24-0318 |
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creator | PURBA, Melpa Susanti ANGGORO, Dito ITOH, Harumichi ITAMOTO, Kazuhito NEMOTO, Yuki NAKAICHI, Munekazu SUNAHARA, Hiroshi TANI, Kenji |
description | 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/cm2) 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. |
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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/cm2) 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.</description><identifier>ISSN: 0916-7250</identifier><identifier>ISSN: 1347-7439</identifier><identifier>EISSN: 1347-7439</identifier><identifier>DOI: 10.1292/jvms.24-0318</identifier><identifier>PMID: 39537157</identifier><language>eng</language><publisher>Japan: JAPANESE SOCIETY OF VETERINARY SCIENCE</publisher><subject>Animals ; blue light ; canine fibroblast ; Cell Movement - radiation effects ; Cell Proliferation - radiation effects ; Cell Survival - radiation effects ; Cells, Cultured ; Dogs ; Fibroblasts - radiation effects ; Low-Level Light Therapy - methods ; Low-Level Light Therapy - veterinary ; Mouth Mucosa - cytology ; Mouth Mucosa - radiation effects ; red light ; Surgery ; wound healing ; Wound Healing - radiation effects</subject><ispartof>Journal of Veterinary Medical Science, 2024, pp.24-0318</ispartof><rights>2024 by the Japanese Society of Veterinary Science</rights><rights>2025 The Japanese Society of Veterinary Science 2025</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2734-dd6c8e924c3c08059932bd9ec8bc7a5e5fed656e6b536a43d447500f0ef9bd063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11735224/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11735224/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,1877,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39537157$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PURBA, Melpa Susanti</creatorcontrib><creatorcontrib>ANGGORO, Dito</creatorcontrib><creatorcontrib>ITOH, Harumichi</creatorcontrib><creatorcontrib>ITAMOTO, Kazuhito</creatorcontrib><creatorcontrib>NEMOTO, Yuki</creatorcontrib><creatorcontrib>NAKAICHI, Munekazu</creatorcontrib><creatorcontrib>SUNAHARA, Hiroshi</creatorcontrib><creatorcontrib>TANI, Kenji</creatorcontrib><title>Effects of low-level laser irradiation on canine fibroblasts</title><title>Journal of Veterinary Medical Science</title><addtitle>J. Vet. Med. Sci.</addtitle><description>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/cm2) 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.</description><subject>Animals</subject><subject>blue light</subject><subject>canine fibroblast</subject><subject>Cell Movement - radiation effects</subject><subject>Cell Proliferation - radiation effects</subject><subject>Cell Survival - radiation effects</subject><subject>Cells, Cultured</subject><subject>Dogs</subject><subject>Fibroblasts - radiation effects</subject><subject>Low-Level Light Therapy - methods</subject><subject>Low-Level Light Therapy - veterinary</subject><subject>Mouth Mucosa - cytology</subject><subject>Mouth Mucosa - radiation effects</subject><subject>red light</subject><subject>Surgery</subject><subject>wound healing</subject><subject>Wound Healing - radiation effects</subject><issn>0916-7250</issn><issn>1347-7439</issn><issn>1347-7439</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE1rGzEQhkVpaJy0t57LHnPoJvrWCgohBCdtMOSSnIVWGjky8iqV1i7991ljx7QgGME888zwIvSV4EtCNb1abdf1kvIWM9J9QDPCuGoVZ_ojmmFNZKuowKforNYVxpRwqT-hU6YFU0SoGfoxDwHcWJscmpT_tAm2kJpkK5QmlmJ9tGPMQzM9Z4c4QBNiX3I_EWP9jE6CTRW-HOo5er6bP93-bBeP979ubxato4rx1nvpOtCUO-Zwh4XWjPZeg-t6p6wAEcBLIUH2gknLmedcCYwDhqB7jyU7R9d77-umX4N3MIzFJvNa4tqWvybbaP7vDPHFLPPWEKKYoJRPhouDoeTfG6ijWcfqICU7QN5UwwjtOtJx2U3o9z3qSq61QDjuIdjsEje7xA3lZpf4hH_797Yj_B7xBDzsgVUd7RKOgC1jdAn2Nuu307zB75-D_Qi5F1sMDOwND-yZ3A</recordid><startdate>20250110</startdate><enddate>20250110</enddate><creator>PURBA, Melpa Susanti</creator><creator>ANGGORO, Dito</creator><creator>ITOH, Harumichi</creator><creator>ITAMOTO, Kazuhito</creator><creator>NEMOTO, Yuki</creator><creator>NAKAICHI, Munekazu</creator><creator>SUNAHARA, Hiroshi</creator><creator>TANI, Kenji</creator><general>JAPANESE SOCIETY OF VETERINARY SCIENCE</general><general>The Japanese Society of Veterinary Science</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20250110</creationdate><title>Effects of low-level laser irradiation on canine fibroblasts</title><author>PURBA, Melpa Susanti ; ANGGORO, Dito ; ITOH, Harumichi ; ITAMOTO, Kazuhito ; NEMOTO, Yuki ; NAKAICHI, Munekazu ; SUNAHARA, Hiroshi ; TANI, Kenji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2734-dd6c8e924c3c08059932bd9ec8bc7a5e5fed656e6b536a43d447500f0ef9bd063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Animals</topic><topic>blue light</topic><topic>canine fibroblast</topic><topic>Cell Movement - radiation effects</topic><topic>Cell Proliferation - radiation effects</topic><topic>Cell Survival - radiation effects</topic><topic>Cells, Cultured</topic><topic>Dogs</topic><topic>Fibroblasts - radiation effects</topic><topic>Low-Level Light Therapy - methods</topic><topic>Low-Level Light Therapy - veterinary</topic><topic>Mouth Mucosa - cytology</topic><topic>Mouth Mucosa - radiation effects</topic><topic>red light</topic><topic>Surgery</topic><topic>wound healing</topic><topic>Wound Healing - radiation effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PURBA, Melpa Susanti</creatorcontrib><creatorcontrib>ANGGORO, Dito</creatorcontrib><creatorcontrib>ITOH, Harumichi</creatorcontrib><creatorcontrib>ITAMOTO, Kazuhito</creatorcontrib><creatorcontrib>NEMOTO, Yuki</creatorcontrib><creatorcontrib>NAKAICHI, Munekazu</creatorcontrib><creatorcontrib>SUNAHARA, Hiroshi</creatorcontrib><creatorcontrib>TANI, Kenji</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Veterinary Medical Science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PURBA, Melpa Susanti</au><au>ANGGORO, Dito</au><au>ITOH, Harumichi</au><au>ITAMOTO, Kazuhito</au><au>NEMOTO, Yuki</au><au>NAKAICHI, Munekazu</au><au>SUNAHARA, Hiroshi</au><au>TANI, Kenji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of low-level laser irradiation on canine fibroblasts</atitle><jtitle>Journal of Veterinary Medical Science</jtitle><addtitle>J. Vet. Med. Sci.</addtitle><date>2025-01-10</date><risdate>2025</risdate><volume>87</volume><issue>1</issue><spage>24-0318</spage><epage>96</epage><pages>24-0318-96</pages><artnum>24-0318</artnum><issn>0916-7250</issn><issn>1347-7439</issn><eissn>1347-7439</eissn><abstract>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/cm2) 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.</abstract><cop>Japan</cop><pub>JAPANESE SOCIETY OF VETERINARY SCIENCE</pub><pmid>39537157</pmid><doi>10.1292/jvms.24-0318</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals blue light canine fibroblast Cell Movement - radiation effects Cell Proliferation - radiation effects Cell Survival - radiation effects Cells, Cultured Dogs Fibroblasts - radiation effects Low-Level Light Therapy - methods Low-Level Light Therapy - veterinary Mouth Mucosa - cytology Mouth Mucosa - radiation effects red light Surgery wound healing Wound Healing - radiation effects |
title | Effects of low-level laser irradiation on canine fibroblasts |
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