摘要
按硫代巴比妥酸法测定了葡萄糖-6-磷酸脱氢酶(G6PD)缺乏和正常红细胞的丙二醛(MDA)含量,按改良Nisselbaum法测定还原型辅酶II(NADPH)的含量。G6PD缺乏红细胞的MDA和NADPH分别为38.74nmol/gHb和1803.6μmol/gHb;正常红细胞中含量则分别为25.60nmol/gHb和2242.8tLmol/gHb。在受到过氧化刺激后,G6PD缺乏红细胞的MDA生成明显大于正常红细胞,NADPH明显减少,而正常红细胞的NADPH则增加。维生素E能保护G6PD缺乏红细胞,使其在过氧化刺激下MDA生成不增加。研究提示,G6PD缺乏红细胞的脂质过氧化损伤比正常严重,其机制是NADPH生成不足。
he malonyldialdehyde(MDA)and NADPH levels were detected in G6PD deficient and normal erythro-cytes.The MDA and NADPH levels were 38.74 nmol/gHb and 1803.6μmol/gHb in G6PD deficient erythrocytes and 25.6nmol/gHb and 2242.8μmol/gHb in normal erythrocytes,respectively. Under oxidative stress,the G6PD deficient erythrocytes generated more MDA than normal.and the NADPH level was increased in normal erythrocytes but decreased inG6PD deficient erythrocytes,Vitamin E could protectG6PD deficient erythrocytes from oxidative damage,the production of MDA did not increase under oxida-tive stress if tbe G6PD deficient ervthrocvtes weretreated with vitamin E .The results indicated that the degree of lipoperoxidation was more severe in G6PDdeficient erythrocytes than in normal ones.The mech-anism of the overlipoperoxidation in G6PD deficienterythrocytes is the insufficient production of NADPH.
出处
《中华血液学杂志》
CAS
CSCD
北大核心
1995年第8期406-408,共3页
Chinese Journal of Hematology
基金
广东省自然科学基金
广东省卫生厅重点科研基金
关键词
红细胞
G6PD缺乏
脂质过氧化
NADPH
Erythrocyte G 6PD deficient Lipoperoxidation Malonvl-dealdehyde NADPH