Curso de Fisioterapia, Universidade do Extremo Sul Catarinense (UNESC), Criciúma, SC, Brasil.
Ultrasound Med Biol. 2012 Aug;38(8):1470-5. doi: 10.1016/j.ultrasmedbio.2012.03.020. Epub 2012 Jun 12.
Studies have shown an exacerbated increase in proinflammatory markers during and after muscle injury. In this way, interventions that reduce inflammatory activation appear to be of great interest in muscle injury therapy. Thus, the preset study evaluated the effect of low-intensity pulsed ultrasound (LIPUS) and dimethylsulfoxide (DMSO) on the proinflammatory molecules in an animal model of traumatic muscle injury. Forty-eight 3-month old male Wistar rats were divided into six groups (n = 8/group): sham; muscle injury without treatment; muscle injury and gel-saline (0.9%); muscle injury and gel-DMSO (15 mg/kg); muscle injury and LIPUS plus gel-saline; and muscle injury and LIPUS plus gel-DMSO. Two, 12, 24 and 48 h after trauma, four groups received one of the treatments described. One hour after, Western blot was performed to quantify proinflammatory protein levels. We observed greater protein levels of TNFα (3.9 times), IL-1β (3.6 times), JNK phosphorylation (4.2 times) and NFκB (3.8 times) in muscle injury group. However, the combined LIPUS with DMSO resulted in significantly lower levels of TNFα (2.2 times), IL-1β (2.1 times), JNK phosphorylation (2.4 times), and NFκB (2.1 times). The results demonstrate that LIPUS associated with DMSO gel can attenuate TNFα, IL-1β, NFκB protein levels and JNK phosphorylation in traumatic muscle injury.
研究表明,在肌肉损伤期间和之后,促炎标志物的增加加剧。因此,干预炎症激活似乎对肌肉损伤治疗非常有意义。因此,本研究评估了低强度脉冲超声(LIPUS)和二甲基亚砜(DMSO)对创伤性肌肉损伤动物模型中促炎分子的影响。将 48 只 3 月龄雄性 Wistar 大鼠分为六组(n = 8/组):假手术组;未治疗的肌肉损伤组;肌肉损伤和凝胶生理盐水组(0.9%);肌肉损伤和凝胶 DMSO 组(15mg/kg);LIPUS 加凝胶生理盐水组;和 LIPUS 加凝胶 DMSO 组。创伤后 2、12、24 和 48 小时,四组接受了上述治疗之一。治疗后 1 小时,进行 Western blot 以定量促炎蛋白水平。我们观察到肌肉损伤组 TNFα(3.9 倍)、IL-1β(3.6 倍)、JNK 磷酸化(4.2 倍)和 NFκB(3.8 倍)的蛋白水平更高。然而,LIPUS 联合 DMSO 导致 TNFα(2.2 倍)、IL-1β(2.1 倍)、JNK 磷酸化(2.4 倍)和 NFκB(2.1 倍)的水平显著降低。结果表明,LIPUS 联合 DMSO 凝胶可减轻创伤性肌肉损伤中 TNFα、IL-1β、NFκB 蛋白水平和 JNK 磷酸化。