Improved Wound Remodeling Correlates with Modulated TGF‐beta Expression in Skin Diabetic Wounds Following Combined Red and Infrared Photobiomodulation Treatments
Diabetic wounds are a major cause of morbidity among patients with poorly controlled blood glucose levels. Conventional empirical wound care strategies have shown limited efficacy, and there is an urgent need to develop novel therapeutic strategies. Photobiomodulation treatments have shown positive...
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Veröffentlicht in: | Photochemistry and photobiology 2018-07, Vol.94 (4), p.775-779 |
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Zusammenfassung: | Diabetic wounds are a major cause of morbidity among patients with poorly controlled blood glucose levels. Conventional empirical wound care strategies have shown limited efficacy, and there is an urgent need to develop novel therapeutic strategies. Photobiomodulation treatments have shown positive therapeutic effects in several cell culture and animal models. In this study, we examined wound healing in diabetic rats following treatments with two laser wavelengths, namely red (660 nm) and infrared (808 nm) individually and in combination as compared to routine wound dressings. Immunostaining for TGF‐β expression was performed at various times postwounding. We noted that the combination of red and infrared laser treatments correlated with decreased TGF‐β1 levels at late stages in healing. There was no statistical significance with any treatments at an earlier time point. This study emphasizes the role of appropriate laser treatment protocols in modulating wound healing and remodeling responses.
Combined treatment with red and infrared laser treatments promotes wound healing and correlates with modulated TGF‐beta1 expression during individual phases. The synergistic combination of dual wavelength for photobiomodulation therapy can not only provide a broader target area but can also potentially invokes discrete therapeutic mechanisms. Abbreviations used: TGF‐β – Transforming Growth Factor‐β; TRPV – Transient Receptor Potential Vanilloid, AHR‐ Aryl Hydrocarbon Receptors; ROS – Reactive Oxygen Species; ATP – Adenosine Trisphosphate. |
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ISSN: | 0031-8655 1751-1097 |
DOI: | 10.1111/php.12914 |