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作 者:崔毓桂[1] 何戎华[1] 朱安[1] 朱学素[1] 黄风云 李燕[1] 汪承亚[1] 陈家伟[1]
出 处:《标记免疫分析与临床》1996年第4期185-188,共4页Labeled Immunoassays and Clinical Medicine
基 金:南京医科大学科研基金
摘 要:胰岛素受体(IR)异常导致胰岛素作用障碍,是Ⅱ型糖尿病(NIDDM)发病中的一个主要因素。本文改良国内外人红细胞IR分析方法,并应用于NIDDM临床实践,取得满意结果。方法学的平均批内变异系数为5.66%,批间变异系数为12.67%。健康人23名(年龄29~70岁),高亲和力IR位点数为224.4±89.8位点/细胞,平衡解离常数Kd=(5.71±0.65)×10-11mol/L;低亲和力IR位点数为2044.9±188.9位点/细胞,Kd=(2.96±0.29)×10-9mol/L。79例NIDDM患者(年龄24~72岁),高亲和力IR位点数为180.6±103.6位点/细胞(P>0.05),但Kd=(8.97±2.14)×10-11mol/L(P<0.05);低亲和力IR位点数为1237.0±495.1位点/细胞,Kd=(6.44±0.98)×10-9mol/L,均与正常组差异显著(P<0.01).表明NIDDM患者IR结合量下降,受体对胰岛素亲和力下降。We developed a radioreceptor assay method for measurement of insulin binding activity of erythrocyte insulin receptor. Altogether 23 normal subjects aged 29 ̄70 ys and 79 patients with noninsulin dependent diabetes mellitus (NIDDM) aged 24 ̄72 ys were included in this study. The maximum of specific binding ratio of erythrocyte insulin receptor was 25. 7±5. 0%, while nonspecific binding ratio was only 4. 3±0. 3%. The within batch coefficient of variation was 5. 66%,and the between assay variation was 12. 67%. So the method was stable,reliable,practicable and easy to perform. Compared with the normal subjects,the insulin binding capacity of insulin receptor of patients with NIDDM and the affinity decreased. The capacity of high-affinity insulin receptor of normal group and NIDDM group were 224. 4±89. 8 and 180. 6±103. 6sites/cell(P>0. 05) ,Kd were (5. 71±0. 65) 10-11mol/ L and (8. 97±2. 14)X10-11 mol/L (P<0. 05) ,respectively. The capacity of low-affinity insulin receptor of two groups were 2044. 9±188. 9 sites/cell and 1237. 0±495. 1sites/cell (P <0. 01),Kd were (2. 96±0. 29)X10-9mol/L and (6. 44±0. 98)X10-9mol/L (P>0.01),respectively. It is suggested that the abnormality of insulin receptor leading to insulin resistance might be one of important factors in the pathogesis of NIDDM.
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