Chen Rong-Fu, Chang Chih-Hau, Wang Chun-Ting, Kuo Yur-Ren
Ann Plast Surg. 2019 Jan;82(1S Suppl 1):S18-S22. doi: 10.1097/SAP.0000000000001723.
Oxygen free radicals play a central role in diabetic angiopathy. This study investigated whether suppression of oxygen radicals could decrease endothelial damage and increase peripheral tissue circulation in a diabetic rodent model.
Sprague-Dawley rats were treated using streptozotocin to induce diabetes. The experiments were performed 4 weeks after diabetes induction: group 1: control, consisted of normal rats; group 2: diabetes, did not receive treatment; groups III (SOD10) and IV (SOD50): diabetes, received polyethylene glycol-conjugated superoxide dismutase (SOD), an antioxidant, 10 and 50 U/kg per day intraperitoneally for 4 weeks. Each subgroup consisted of 10 rats. Oxygen radicals in blood mononuclear cells were detected by flow cytometry. The blood lipid peroxidation byproduct malondialdehyde was measured. Tissue perfusion of hind limb was examined by laser Doppler. The expressions of oxygen radicals, as demonstrated by 8-hydroxyguanosine (8-OG), and constitutive endothelial nitric oxide synthase in distal femoral vessels were examined by immunohistochemical staining.
Oxygen radicals, as demonstrated by H2O2 with 2',7'-dichlorofluorescin diacetate-conjugated expression, were significantly increased in diabetic rats. However, the SOD treatment groups significantly suppressed the H2O2 reaction. Diabetic-induced high malondialdehyde levels were significantly suppressed in the SOD50 group. The topical tissue blood perfusion was significantly increased as detected by laser Doppler in SOD10 and SOD50 groups, as compared with that in diabetes without treatment group (P < 0.05). The expression of 8-OG was markedly increased in the diabetic endothelium and subintima compared with that in normal vessels. Polyethylene glycol-conjugated SOD significantly suppressed 8-OG expression and protected endothelial nitric oxide synthase expression.
Suppression of oxygen radicals, particularly with the higher dosage of polyethylene glycol-conjugated SOD at 50 U/kg per day, could have a positive effect to protect against endothelial damage and enhance peripheral perfusion in diabetes.
氧自由基在糖尿病血管病变中起核心作用。本研究调查了在糖尿病啮齿动物模型中抑制氧自由基是否能减少内皮损伤并增加外周组织循环。
用链脲佐菌素处理斯普拉格-道利大鼠以诱导糖尿病。在糖尿病诱导4周后进行实验:第1组:对照组,由正常大鼠组成;第2组:糖尿病组,未接受治疗;第III组(SOD10)和第IV组(SOD50):糖尿病组,接受抗氧化剂聚乙二醇共轭超氧化物歧化酶(SOD),每天腹腔注射10和50 U/kg,持续4周。每个亚组由10只大鼠组成。通过流式细胞术检测血液单核细胞中的氧自由基。测量脂质过氧化副产物丙二醛。用激光多普勒检查后肢的组织灌注。通过免疫组织化学染色检查股动脉远端血管中由8-羟基鸟苷(8-OG)所示的氧自由基表达和组成型内皮一氧化氮合酶表达。
用二氯荧光素二乙酸酯共轭表达的H2O2所示,糖尿病大鼠中的氧自由基显著增加。然而,SOD治疗组显著抑制了H2O2反应。SOD50组中糖尿病诱导的高丙二醛水平被显著抑制。与未治疗的糖尿病组相比,激光多普勒检测显示SOD10和SOD50组的局部组织血液灌注显著增加(P < 0.05)。与正常血管相比,糖尿病内皮和内膜中8-OG的表达明显增加。聚乙二醇共轭SOD显著抑制8-OG表达并保护内皮一氧化氮合酶表达。
抑制氧自由基,特别是每天50 U/kg的较高剂量聚乙二醇共轭SOD,可能对预防糖尿病中的内皮损伤和增强外周灌注有积极作用。