2020
DOI: 10.1007/s10103-019-02941-y
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Attenuation of the inflammatory response and polarization of macrophages by photobiomodulation

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Cited by 23 publications
(18 citation statements)
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“…Moreover, many studies have demonstrated the anti-inflammatory effects of PBM [41,42]. PBM is able to modulate mRNA gene expression of IL-10 in acute and chronic inflammatory phase and decreases the expression of this cytokine and consequently modulates the inflammatory process of OA [43]. Taking together, the combined treatments presented a positive effect on IL-10 expression, which could represent a modulation of the inflammatory process.…”
Section: Discussionmentioning
confidence: 98%
“…Moreover, many studies have demonstrated the anti-inflammatory effects of PBM [41,42]. PBM is able to modulate mRNA gene expression of IL-10 in acute and chronic inflammatory phase and decreases the expression of this cytokine and consequently modulates the inflammatory process of OA [43]. Taking together, the combined treatments presented a positive effect on IL-10 expression, which could represent a modulation of the inflammatory process.…”
Section: Discussionmentioning
confidence: 98%
“…The most relevant proposed theory with regard to the current study is the notion of how low‐level laser PBM treatment alters macrophage state detailed by recent independent studies conducted by de Brito et al and Li et al 46,47 PBMs have the ability to alter the phenotype of activated cells in macrophages, and these cells have very different phenotypes depending on the pathological condition. Inducible nitric oxide synthase (iNOS) is a characteristic of the M1 phenotype and nitric oxide secretion is often measured.…”
Section: Discussionmentioning
confidence: 99%
“…Our team has focused on optimizing PBM and exploring the underlying mechanism. Previous data have shown that PBM can facilitate alternatively activated macrophage/microglia polarization, relieve secondary neuroinflammation, and improve the ability of neurons to resist insults caused by trauma [ 15 , 16 , 44 , 45 ]. However, in the corresponding studies, PBM was applied transcutaneously at the lesion site, and only a small dose of energy (approximately 6%) was able to penetrate tissue and reach the spinal cord surface, according to reports [ 39 , 46 ].…”
Section: Discussionmentioning
confidence: 99%
“…Signaling associated with inflammation, such as mitogen-activated protein kinase (MAPK) signaling, nuclear factor kappa-Β (NF-κB) signaling, c-Jun N-terminal kinase (JNK) signaling, and Toll-like receptor (TLR)/myeloid differentiation primary response 88 (MYD88) pathway signaling, is suppressed by PBM; in contrast, the phosphatidylinositol 3-kinase (PI3K)/Akt pathways, extracellular signal-regulated kinase (ERK)/cyclic adenosine monophosphate-responsive element binding protein (CREB) pathways, and transforming growth factor-β (TGF-β)/Smad signaling pathways can be upregulated by PBM [ 59 63 ]. In cultured cells treated with PBM, the expression of GFAP and the secretion of cartilage sulfate proteoglycans (CSPGs) by primary astrocytes are decreased [ 16 ]; the levels of ROS and the axon retraction of dorsal root ganglion (DRG) neurons under oxidative stress conditions are improved [ 64 ]; NF-κB signaling in the activation of M1-type BMDM polarization is inhibited; and the protein kinase A (PKA)/CREB pathway participating in M2 polarization is activated [ 44 , 45 ]. Our findings will contribute to clarification of the biochemical mechanism of PBM, especially since the roles of microglia and astrocytes in neuroinflammation have received increasing attention.…”
Section: Discussionmentioning
confidence: 99%