Okubo T
Second Department of Surgery, Hokkaido University School of Medicine, Sapporo, Japan.
Hokkaido Igaku Zasshi. 1993 Sep;68(5):665-82.
We examine influences of immunosuppression on wound healing, using C57BL/6 mice by carrageenan, anti-asialo GM 1 antibody and Cyclosporin A (CSA). Mice underwent a standardized dorsal skin incision and subcutaneous implantation of sterile polyvinyl alcohol sponge under ether anesthesia. They were sacrificed on the 14th and 21st day after wounding. The pelts excised, and fresh breaking strength was measured with a constant-speed tensiometer. The sponges were removed, and hydroxyproline was measured by Woessner's method. 1) Sixteen mice were divided into 2 groups, eight mice intraperitoneally received carrageenan to suppress macrophage function twice before and after wounding, and eight mice, as a control, received saline in the same way. The breaking strength in the carrageenan-treated mice was weaker than in the control on the 14th day and 21st day. Hydroxyproline content was not different between the treated group and control. 2) Sixteen mice were divided into 2 groups, eight mice intraperitoneally received anti-asialo GM 1 antibody to suppress natural killer cell function twice before and after wounding, and eight mice, as a control, received saline in the same way. The breaking strength in the anti-asialo GM 1 antibody treated mice was not significantly different from that in the control on the 14th or 21st day. Hydroxyproline content was not different in the treated group and control. 3) Thirty two mice were divided into 4 groups, eight mice intraperitoneally received CSA at a dose of 1.0 mg/kg twice before and after wounding, eight mice received CSA at a dose of 10.0 mg/body, eight mice received CSA at a dose of 100.0 mg/body to suppress T helper lymphocyte function, and eight mice, as a control, received Intralipos at a dose of 1.0 g/kg in the same way. The breaking strength in the 10.0 mg/kg and 100.0 mg/kg CSA-treated mice were weaker than in the control on the 14th day. There was no significant difference on the 21st day. The breaking strength in the 1.0 mg/kg treated mice was not different from in the control on the 14th day or 21st day. Histologically, there was no difference between CSA-treated group and control. 4) Forty mice were divided into 4 groups, twenty mice received CSA at a dose of 40.0 mg/kg for once a day for 7 days before and 14 days after wounding respectively, twenty mice received Intralipos at a dose of 1.0 g/kg in the same way.(ABSTRACT TRUNCATED AT 400 WORDS)
我们使用C57BL/6小鼠,通过角叉菜胶、抗去唾液酸GM1抗体和环孢素A(CSA)来研究免疫抑制对伤口愈合的影响。小鼠在乙醚麻醉下接受标准化的背部皮肤切口,并皮下植入无菌聚乙烯醇海绵。在受伤后的第14天和第21天对它们实施安乐死。切除皮肤,用恒速张力计测量新鲜皮肤的断裂强度。取出海绵,采用沃斯纳法测量羟脯氨酸含量。1)16只小鼠分为2组,8只小鼠在受伤前后两次腹腔注射角叉菜胶以抑制巨噬细胞功能,另外8只小鼠作为对照,以同样方式注射生理盐水。在第14天和第21天,接受角叉菜胶处理的小鼠的断裂强度比对照组弱。处理组和对照组的羟脯氨酸含量没有差异。2)16只小鼠分为2组,8只小鼠在受伤前后两次腹腔注射抗去唾液酸GM1抗体以抑制自然杀伤细胞功能,另外8只小鼠作为对照,以同样方式注射生理盐水。在第14天或第21天,接受抗去唾液酸GM1抗体处理的小鼠的断裂强度与对照组没有显著差异。处理组和对照组的羟脯氨酸含量没有差异。3)32只小鼠分为4组,8只小鼠在受伤前后两次腹腔注射剂量为1.0mg/kg的CSA,8只小鼠接受剂量为10.0mg/只的CSA,8只小鼠接受剂量为100.0mg/只的CSA以抑制辅助性T淋巴细胞功能,另外8只小鼠作为对照,以同样方式注射剂量为1.0g/kg的静脉注射脂肪乳剂。在第14天,接受10.0mg/kg和100.0mg/kg CSA处理的小鼠的断裂强度比对照组弱。在第21天没有显著差异。在第14天或第21天,接受1.0mg/kg处理的小鼠的断裂强度与对照组没有差异。组织学上,CSA处理组和对照组之间没有差异。4)40只小鼠分为4组,20只小鼠在受伤前7天和受伤后14天分别每天一次接受剂量为40.0mg/kg的CSA,另外20只小鼠以同样方式接受剂量为1.0g/kg的静脉注射脂肪乳剂。(摘要截选至400字)