2017
DOI: 10.1136/acupmed-2016-011107
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Electroacupuncture Alleviates the Inflammatory Response via Effects on M1 and M2 Macrophages after Spinal Cord Injury

Abstract: EA had a positive impact on SCI model rats. This may be related to the neuroprotective effect of NT-3, which may increase the polarisation of M2 microglia/macrophages.

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Cited by 39 publications
(34 citation statements)
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“…CP is a group of permanent disorders of the development of movement and posture that appear in early childhood, 3 which causes activity limitation that is attributed to non-progressive disturbances that occurred in the developing fetal or infant brain. 1 Moreover, MLEC significantly decreased IL-1b, a major secreted cytokine of M1 macrophage, 24 and significantly increased the expression of Mrc1 and Mgl2, makers of M2 macrophage, 25 and enhanced the arginase activity, indicator of M2 polarization, 26 in RAW264.7 cells. These results indicated that MLEC promotes the M1 to M2 macrophage polarization.…”
Section: Discussionmentioning
confidence: 96%
“…CP is a group of permanent disorders of the development of movement and posture that appear in early childhood, 3 which causes activity limitation that is attributed to non-progressive disturbances that occurred in the developing fetal or infant brain. 1 Moreover, MLEC significantly decreased IL-1b, a major secreted cytokine of M1 macrophage, 24 and significantly increased the expression of Mrc1 and Mgl2, makers of M2 macrophage, 25 and enhanced the arginase activity, indicator of M2 polarization, 26 in RAW264.7 cells. These results indicated that MLEC promotes the M1 to M2 macrophage polarization.…”
Section: Discussionmentioning
confidence: 96%
“…The histological outcomes were consistent with the functional improvement, which indicates that EA is important in neurologic recovery after SCI. Although several mechanisms mediate the effect of EA on SCI [13][14][15][16][17], the inhibition of inflammatory response and oxidative stress by EA is primary and important factors [20][21][22] It is well known that ApoE contributes to modulating neuronal repair and remodeling in CNS trauma and diseases [75,76], which owes to its anti-inflammatory, anti-oxidative stress and anti-apoptotic…”
Section: Discussionmentioning
confidence: 99%
“…Several reports show that EA could effectively facilitate the cell survival and reduce the neurons apoptosis [13][14][15], prompt neural stem cell or precursor cells to proliferate and differentiate into neurons [16,17], accelerate axonal regeneration and remyelination [18,19] after SCI. In particular, recent reports have shown that EA could alleviate inflammatory response via inhibiting the activation of NF-kB signaling pathway or microglia cells [20,21], or downregulating the M1 macrophages markers as well as upregulating the M2 macrophages markers [22]. EA can also control oxidative stress by reducing the amount of reactive species and increase the activity of the antioxidant enzymes superoxide dismutase and glutathione peroxidase in experimental rat models [23].…”
Section: Introductionmentioning
confidence: 99%
“…In rats with spinal cord injuries, EA treatment altered the ratio of M1/M2 macrophages. EA treatment suppressed the M1 subtypeby downregulating the marker protein CD68 and reducing TNF-α, IL-1β, and IL-6 levels, while simultaneously enhancing the proportion of M2, upregulating the marker proteins CD206 and NT-3 and increasing expression levels of IL-10 [42]. Similar findings were revealed in a study conducted by da Silva and colleagues [43], where they demonstrated that MA resulted in analgesic and anti-inflammatory effects in a rat model of muscle pain, accompanied by an M1 to M2 shift in the macrophage population and increased IL-10 expression levels.…”
Section: Attenuation Of Systemic Inflammation Andmentioning
confidence: 99%