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机构地区:[1]泰安市中心医院内分泌科,山东省泰安271000
出 处:《中国医师杂志》2011年第6期769-771,775,共4页Journal of Chinese Physician
摘 要:目的检测糖尿病肾病患者血清蛋白氧化损伤指标的变化,探讨蛋白氧化损伤在糖尿病肾病发病中的可能机制。方法应用改良后的Witko—Sarsat法和2,4-二硝基苯肼法检测血清晚期氧化蛋白产物(AOPP)水平、蛋白质羰基(PCO)含量,应用ELISA及酶谱法分别检测血清基质金属蛋白酶-2(MMP-2)的表达水平和活性。结果DNl组、DN2组AOPP水平明显高于DM组(78.23±19.30VS61.25±12.13、101.59±30.22VS61.25±12.13,F=41.988,P〈0.01),DNl组、DN2组PCO含量亦明显高于DM组(0.84±0.03VS0.66±0.02、1.05±0.05VS0.66±0.02,F=205.763,P〈0.01),AOPP、PCO与血清MMP-2的表达水平(r=0.460,0.480,P〈0.05)和活性(r=0.385,0.560,P〈0.05)均呈正相关,多元逐步回归分析表明AOPP、PCO为血清MMP-2表达水平(P〈0.05,P〈0.01)和活性(P〈0.01,P〈0.05)的主要影响因素。结论推测蛋白氧化损伤通过改变MMP-2的表达和活性,影响肾脏基质代谢。Objective Serum indicators of oxidative protein damage (OPD) were analyzed to explore the effect on renal MMP/TIMP system of OPD in diabetic nephropathy. Methods AOPP levels and PCO levels were measured by modified Witko-Sarsat's method and 2, 4-dinitrophenylhydrazine spectrophoto- metric method, expression of serum MMP-2 were determined by ELISA, and MMP-2 activity were detected by zymography . Results AOPP levels of group DN1, group DN2 were higher than those of group DM ( 78. 23 ±19. 30 vs 61. 25 ±12.13 ,101. 59 ± 30. 22 vs 61. 25 ±12.13 , F =41.988,P 〈0.01). PCOlev- els of group DN1 and group DN2 were higher than those of group DM (0. 84 ±0. 03 vs 0. 66 ±0. 02,1.05 ± 0. 05 vs 0. 66 ± 0. 02, F = 205. 763, P 〈 0. 01 ). Pearson correlation analysis indicated AOPP and PCO were positively correlated with the expression ( r = 0. 460,0. 480, P 〈 0. 05 ) and activity ( r = 0. 385, 0. 560, P 〈 0. 05 ) of serum MMP-2. Multiple stepwise regression analysis showed that AOPP and PCO were major influential factors of serum MMP-2 expression ( P 〈0. 05, P 〈0. 01 ) and activity( P 〈0. 01 , P 〈 0. 05 ). Conclusions OPD might be involved in the imbalance of renal matrix metabolism, which was correlated with the development of diabetic nephropathy.
关 键 词:糖尿病肾病/代谢 DNA损伤 基质金属蛋白酶2/代谢 蛋白水解产物/代谢
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