机构地区:[1]上海交通大学医学院附属瑞金医院上海市烧伤研究所,200025
出 处:《中华烧伤杂志》2011年第1期21-25,共5页Chinese Journal of Burns
基 金:基金项目:国家自然科学基金(30700871、30600645);国家重点基础研究发展规划(2005CB522603)
摘 要:目的观察外敷氨基胍霜剂对糖尿病大鼠皮肤组织晚期糖基化终末产物(AGE)形成、Kc细胞增殖及氧化应激的影响。方法将硬脂酸、液状石蜡、凡士林、羊毛脂、肉豆蔻酸异丙酯、甘油、50g/L尼泊金醇、盐酸氨基胍等试剂按一定比例混合制成氨基胍霜剂,以不含有氨基胍的霜剂为基质。取健康大鼠背部皮肤,分别用5、10g/L氨基胍霜剂和5g/L氨基胍+10g/L氮酮霜剂处理,于用药后2、4、7、10、12、24h测定药物透皮效果。将30只SD大鼠按随机数字表法分为正常对照组6只、糖尿病组8只、氨基胍治疗组8只、基质治疗组8只。后3组大鼠腹腔注射链脲佐菌素65mg/kg,诱导糖尿病模型;对照组大鼠注射0.05mmol/L柠檬酸缓冲液。注射1周后,正常对照组与糖尿病组大鼠不行任何治疗,氨基胍治疗组与基质治疗组大鼠背部分别连续外用10g/L氨基胍霜剂与基质治疗4周。取各组皮肤组织,胶原提取液荧光强度检测法测定AGE含量,流式细胞仪分析表皮KC周期,检测氧化应激相关指标超氧化物歧化酶(SOD)、丙二醛、总抗氧化能力、髓过氧化物酶(MPO)含量。对实验数据行t检验。结果10g/L氨基胍霜剂透皮效果优于5g/L氨基胍和5g/L氨基胍+10g/L氮酮的霜剂。1只基质治疗组大鼠未诱导成功。建模后4周,糖尿病组与氨基胍治疗组大鼠分别死亡4只和1只。糖尿病组大鼠皮肤组织AGE含量为每毫克羟脯氨酸(OHP)中(36.8±2.6)U,明显高于正常对照组的每毫克OHP中(24.6±2.7)u(t=7.2,P〈0.01);氨基胍治疗组AGE含量为每毫克OHP中(28.6±3.7)u,明显低于糖尿病组(t=-3.9,P〈0.05);基质治疗组AGE含量[每毫克OHP中(32.2±5.2)U]与糖尿病组相近(t=1.6,P〉0.05)。糖尿病组大鼠S期KC比例为(5.3±0.6)%,低于正常对照组的(7.6±0.9)%(t=4.50,PObjective To investigate the effects of aminoguanidine cream on the proliferation of keratinoeytes (KC) , content of advanced glycosylation end products (AGE) and oxidative stress in skin tissue of rats with diabetes. Methods Stearie acid, liquid paraffin, vaseline, lanolin, isopropyl myristate fat, glycerol, 50 g/L alcohol paraben, aminoguanidine hydrochloride etc. were mixed in certain proportion to make aminoguanidine eream, and cream without aminoguanidine was used as matrix. The dorsal skin of norreal rats were harvested and treated by aminoguanidine cream with dose of 5, 10 g/L, or 5 g/L together with 10 g/L azone. The transdermal effect was respectively measured at post treatment hour :2, 4, 7, 10, 12, 24. Thirty SD rats were divided into normal control ( NC, n = 6) , diabetes ( D, n = 8 ) , aminoguanidine cream-interfered (AI, n = 8) , matrix cream-interfered groups (MI, n = 8) according to the random number table. Diabetes was reproduced by intraperitoneal injection of STZ (65 mg/kg) in rats of D, AI, and MI groups, and rats in NC group were injected with 0.05 mmol/L citrate buffer as control. One week later, dorsal skin of rats in AI and MI groups were respectively treated with 10 g/L aminoguanidine cream and matrix cream by external use for 4 weeks. AGE content was determined with fluorescence detection from skin colla- gen extract. KC cell cycle was detected by flow cytometry. Skin tissue specimens were obtained for determination of levels of superoxide dismutase (SOD), malondialdehyde (MDA), myeloperoxidase (MPO), and total antioxidant capacity. Data were processed with t test. Results Transdermal effect of aminoguanidine cream with dose of 10 g/L was better than that with 5 g/L or 5 g/L + 10 g/L azone cream. One rat was not induced successfully in MI group. Four weeks after model reproduction, 4 rats died in D group and 1 rat died in AI group. The AGE content in D group was obviously higher than that in NC group [ (36.8 ± 2.6) , (24.6 ±2.7) U per
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