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机构地区:[1]中南大学湘雅医院内分泌科,湖南长沙410008 [2]中南大学行政管理学院,湖南长沙410083
出 处:《西安交通大学学报(医学版)》2009年第4期426-429,共4页Journal of Xi’an Jiaotong University(Medical Sciences)
基 金:国家自然科学基金资助项目(No .30570756/C0303021)~~
摘 要:目的观察rAAV2/1-Acrp30对动脉粥样硬化GK大鼠模型血清可溶性细胞间黏附分子(sICAM-1)、可溶性血管内皮黏附分子(sVCAM-1)水平和NF-κB表达的影响,从血管炎症的角度探讨脂联素对糖尿病大血管病变的作用。方法将造模成功的30只动脉粥样硬化的GK大鼠分为三个处理组:①模型1组,后肢肌肉注射盐水;②模型2组,后肢肌肉注射空病毒rAAV2/1;③治疗组,后肢肌肉注射rAAV2/1-Acrp30。治疗8周后处死所有大鼠,比较三组之间血清sICAM-1,sVCAM-1及主动脉处NF-κBp65 mRNA的表达水平。结果治疗组和模型1组、模型2组比较,血清sVCAM-1、sICAM-1显著降低(P<0.05)。治疗组和模型1组、模型2组比较,主动脉NF-κBp65 mRNA表达显著下调(P<0.05)。结论rAAV2/1-Acrp30可通过抑制NF-κB的表达,减轻炎症反应而对糖尿病大血管病变产生保护作用。Objective To study the effects of rAAV2/1-Acrp30 on sICAM-1 and sVCAM-1 level as well as NF-kB expression in GK rats with diabetic arteriosclerosis so as to explore the effect of adiponectin on diabetic macroangiopathy. Methods A total number of 30 atherosclerotic GK rat models were randomly divided into three groups: ① Model group one (M1) hind limb intramuscular injection of normal saline; ② Model group two (M2) : hind limb intramuscular injection of vacuity virus rAAV2/1; Q Treatment group (T): hind limb intramuscular injection of rAAV2/1 -Acrp30 at a dose of 1 × 10n mg/L. After 8 weeks' treatment, the rats were killed, and serum sVCAM-1 and sICAM-1 level as well as aortic NF-kBp65mRNA expression were measured in each group. Aortic NF-kBp65mRNA expression was measured by RT-PCR.Results Compared with those in control model groups (M1 and M2), sVCAM-1 and sICAM-1 levels were decreased significantly in the treatment (T) group (P〈0.05). Aortic NF-kBp65 mRNA expression was significantly down-regulated in the treatment (T) group compared with that in control model groups (M1 and M2) (P 〈0.05). Conclusion rAAV2/1-Acrp30 may produce protective effects on diabetic atherosclerosis by decreasing inflammatory reactions.
关 键 词:脂联素 2型糖尿病大血管病变 核转录因子 可溶性细胞间黏附分子 可溶性血管内皮黏附分子
分 类 号:R764.43[医药卫生—耳鼻咽喉科]
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