Evidence map›Paper›PMID 41566063›Full record

ArticleLasers in medical science2026

Infrared low-level laser therapy enhances proliferation and viability in murine osteoblasts in vitro.

Brenda Lizbeth Arroyo Reyes, Luis G Vázquez-de-Lara-Cisneros, Fabian Galindo Ramírez, Ruben Ramos García, P Zaca Morán

Abstract read
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Article in Lasers in medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Brenda Lizbeth Arroyo ReyesInstituto de Fisiología, Benemérita Universidad Autónoma de Puebla, 72570, Puebla City, Mexico. brenda.arroyore@alumno.buap.mx.
Luis G Vázquez-de-Lara-CisnerosFacultad de Medicina, Benemérita Universidad Autónoma de Puebla, 72410, Puebla City, Mexico.
Fabian Galindo RamírezInstituto de Fisiología, Benemérita Universidad Autónoma de Puebla, 72570, Puebla City, Mexico.
Ruben Ramos GarcíaCoordinación de Óptica, Instituto Nacional de Astrofísica, Óptica y Electrónica, 72840, Puebla City, Mexico.
P Zaca MoránInstituto de Ciencias, Benemérita Universidad Autónoma de Puebla, 72960, Puebla City, Mexico. placido.zaca@correo.buap.mx.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeInfrared low-level laser therapy (LLLT) has shown great promise in promoting cell proliferation and viability, making it a valuable tool in regenerative medicine. This study investigated how the interval between sessions shapes the response to 970 nm LLLT in murine osteoblast cultures by delivering three 10 J/cm² sessions separated by 24-48 h and measuring proliferation, reactive oxygen species (ROS), cytotoxicity, and apoptosis, with the goal of informing protocol design for bone regeneration.

methodsTwo osteoblast cultures were used, one control and the other LLL-treated group. The latter consisted of three irradiation sessions (10 J/cm

resultsThe experimental results showed a significant increase in cell proliferation after two and three sessions (p < 0.05), while ROS levels progressively accumulated, peaking after the third session (p < 0.001). Cell viability remained above 90% in both groups during the first 48 h; however, a slight but significant reduction was observed in the LLLT group at 96 h. Apoptosis levels were lower in LLLT-treated cells during early phases (24-48 h), suggesting a transient cytoprotective effect that diminished after the third session. These findings indicate that infrared LLLT promotes cell proliferation without inducing cytotoxicity or programmed cell death.

conclusionThe results demonstrate that applying three infrared LLLT sessions of 10 J/cm² applied at 24, 48, and 96 h promotes osteoblastic proliferation and viability without inducing cytotoxicity or apoptosis. The proposed protocol, defined by energy dose and irradiation timing, provides a safe and effective strategy for bone tissue engineering.

Indexed as

Cell ProliferationInfrared RaysLow-Level Light TherapyOsteoblastsAnimalsApoptosisBone RegenerationCells, CulturedCell SurvivalMiceReactive Oxygen SpeciesReactive Oxygen SpeciesBone regenerationIn vitroLLLTOsteoblasts

Identifiers

PMID41566063
PMCPMC12823643

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.