Effects of low-level laser therapy on expression of TNF-[alpha] and TGF-[beta] in skeletal muscle during the repair process
The aim of the present study was to determine the effect of low-level laser therapy (LLLT) on the expression of TNF-α and TGF-β in the tibialis anterior muscle of rats following cryoinjury. Muscle regeneration involves cell proliferation, migration and differentiation and is regulated by growth fact...
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Veröffentlicht in: | Lasers in medical science 2011-05, Vol.26 (3), p.335 |
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Sprache: | eng |
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Zusammenfassung: | The aim of the present study was to determine the effect of low-level laser therapy (LLLT) on the expression of TNF-α and TGF-β in the tibialis anterior muscle of rats following cryoinjury. Muscle regeneration involves cell proliferation, migration and differentiation and is regulated by growth factors and cytokines. A growing body of evidence suggests that LLLT promotes skeletal muscle regeneration by reducing the duration of acute inflammation and accelerating tissue repair. Adult male Wistar rats (n=35) were randomly divided into three groups: control group (no lesion, untreated, n=5), cryoinjury without LLLT group (n=15), and cryoinjury with LLLT group (n=15). The injured region was irradiated three times a week using an AlGaInP laser (660 nm; beam spot 0.04 cm^sup 2^, output power 20 mW, power density 500 mW/cm^sup 2^, energy density 5 J/cm^sup 2^, exposure time 10 s). Muscle remodeling was evaluated at 1, 7 and 14 days (long-term) following injury. The muscles were removed and total RNA was isolated using TRIzol reagent and cDNA synthesis. Real-time polymerase chain reactions were performed using TNF-α and TGF-β primers; GAPDH was used to normalize the data. LLLT caused a decrease in TNF-α mRNA expression at 1 and 7 days following injury and in TGF-β mRNA expression at 7 days following cryoinjury in comparison to the control group. LLLT modulated cytokine expression during short-term muscle remodeling, inducing a decrease in TNF-α and TGF-β.[PUBLICATION ABSTRACT] |
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ISSN: | 0268-8921 1435-604X |
DOI: | 10.1007/s10103-010-0850-5 |