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Therapeutic potential of pravastatin for random skin flaps necrosis: involvement of promoting angiogenesis and inhibiting apoptosis and oxidative stress

机译:普伐他汀治疗随机性皮瓣坏死的治疗潜力:参与促进血管生成,抑制细胞凋亡和氧化应激

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Background: Random skin flap is frequently used in plastic and reconstructive surgery, but its distal part often occurs ischemia and necrosis. Pravastatin (Prava) with bioactivities of pro-angiogenesis, anti-apoptosis and anti-oxidative stress, may be beneficial for flap survival. Materials and methods: A modified McFarlane flap model was performed in Sprague-Dawley rats. The animals were divided into the Control and Prava groups and treated as follows: the Prava group was injected intraperitoneally with 2 mg/kg Prava for consecutive 7 days, and the Control group received an equal volume of vehicle daily. On day 7, the necrosis skin flaps were observed, while visualization of blood flow below the tissue surface was performed by Laser Doppler blood flow imaging (LDBFI). Then animals were euthanized, and levels of angiogenesis, apoptosis and oxidative stress were analyzed. Results: Prava decreased necrosis and edema of skin flaps compared with the Control group, with more blood flow in the flap under LDBFI. Prava treatment increased the mean vessels density, elevated the expression levels of angiogenic proteins (matrix metallopeptidase 9, vascular endothelial growth factor, Cadherin5) and antioxidant proteins (superoxide dismutase 1 (SOD1), endothelial nitric oxide synthase, heme oxygenase), and decreased the expression of apoptotic factors (BAX, CYC, Caspase3). In addition, malondialdehyde content was reduced, and glutathione level and SOD activity were increased in the skin flaps after treatment with Prava. Conclusion: Prava promotes survival of random skin flap through induction of angiogenesis, and inhibition of apoptosis and oxidative stress.
机译:背景:随机皮瓣常用于整形和重建手术,但其远端经常发生局部缺血和坏死。普伐他汀(Prava)具有促血管生成,抗凋亡和抗氧化应激的生物活性,可能对皮瓣存活有利。材料和方法:在Sprague-Dawley大鼠中进行改良的McFarlane皮瓣模型。将动物分为对照组和Prava组,并按以下方法进行处理:Prava组连续7天腹膜内注射2 mg / kg Prava,对照组每天接受等量的媒介物。在第7天,观察到坏死的皮瓣,同时通过激光多普勒血流成像(LDBFI)观察组织表面以下的血流。然后将动物安乐死,并分析血管生成,凋亡和氧化应激的水平。结果:与对照组相比,Prava减少了皮瓣的坏死和水肿,LDBFI下皮瓣的血流量增加。 Prava处理可增加平均血管密度,提高血管生成蛋白(基质金属肽酶9,血管内皮生长因子,Cadherin5)和抗氧化剂蛋白(超氧化物歧化酶1(SOD1),内皮型一氧化氮合酶,血红素加氧酶)的表达水平,并降低凋亡因子(BAX,CYC,Caspase3)的表达。此外,用Prava治疗后,皮瓣中丙二醛含量降低,谷胱甘肽水平和SOD活性增加。结论:Prava通过诱导血管生成,抑制细胞凋亡和氧化应激,促进皮肤随机皮瓣的存活。

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