Zhong Shi-long, Zhou Shu-Feng, Chen Xiao, Chan Sui Yung, Chan Eli, Ng Ka-Yun, Duan Wei, Huang Min
Department of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, 74 Zhongshan Er Road, Guangzhou 510080, PR China.
Eur J Pharm Sci. 2006 May;28(1-2):77-85. doi: 10.1016/j.ejps.2006.01.002. Epub 2006 Feb 20.
Glutathione S-transferases (GSTs) are the major detoxifying Phase II enzyme for eliminating electrophilic compounds. Mutations in GSTM1, GSTP1 and GSTT1 in Caucasian and GSTA1 in Chinese have been found to reduce enzyme activity. However, data on the impact of common genetic polymorphisms of GSTM1 and GSTP1 on enzyme activity in Chinese is lacking. This study aimed to investigate the effect of common GSTP1 and GSTM1 polymorphisms on erythrocyte GST activity in healthy Chinese (n = 196). GSTM1 null mutation (GSTM10) was analyzed by a PCR-Multiplex procedure, whereas GSTP1 313A-->G polymorphism (resulting in Ile105Val at codon 105) was analyzed by PCR-restriction fragment length polymorphism (RFLP) analysis. Erythrocyte GST activity was measured using 1-chloro-2,4-dinitro-bezene (CDNB) as the model substrate. The frequency of GSTM1 null genotype was 54.3% and the frequency of GSTP1-Ile/Ile, -Ile/Val, and -Val/Val genotype was 60.7%, 35.2% and 4.1%, respectively, with a frequency of 21.7% for the 105 valine allele. Age, gender and smoking did not significantly affect the erythrocyte GST activities. The mean erythrocyte GST enzyme activity for GSTP1-Ile/Val genotype group (3.53 +/- 0.63U/gHb) was significantly lower than that for subjects with GSTP1-Ile/Ile genotype (4.25 +/- 1.07U/gHb, P = 0.004), while subjects with the GSTP1-Val/Val genotype had the lowest enzyme activity (2.44 +/- 0.67U/gHb). In addition, the GST activity in carriers of GSTM10/GSTP1-Ile/Ile was significantly higher than that of subjects inherited GSTM10/GSTP1-Ile/Val or GSTM1*0/GSTP1-Val/Val. However, there is no association between GSTM1 null mutation and reduced enzyme activity. GSTP1 codon 105 mutation led to reduced erythrocyte GST activity in Chinese. A combined GSTP1 and GSTM1 null mutations also resulted in significantly reduced GST activity. Further studies are needed to explore the clinical implications of GSTM1 and GSTP1 polymorphisms.
谷胱甘肽S-转移酶(GSTs)是用于清除亲电化合物的主要解毒II相酶。已发现白种人中GSTM1、GSTP1和GSTT1以及中国人中GSTA1的突变会降低酶活性。然而,关于GSTM1和GSTP1常见基因多态性对中国人酶活性影响的数据尚缺乏。本研究旨在调查常见的GSTP1和GSTM1多态性对健康中国人(n = 196)红细胞GST活性的影响。通过PCR-多重程序分析GSTM1无效突变(GSTM10),而通过PCR-限制性片段长度多态性(RFLP)分析GSTP1 313A→G多态性(导致密码子105处的Ile105Val)。以1-氯-2,4-二硝基苯(CDNB)作为模型底物测量红细胞GST活性。GSTM1无效基因型的频率为54.3%,GSTP1-Ile/Ile、-Ile/Val和-Val/Val基因型的频率分别为60.7%、35.2%和4.1%,105缬氨酸等位基因的频率为21.7%。年龄、性别和吸烟对红细胞GST活性无显著影响。GSTP1-Ile/Val基因型组的平均红细胞GST酶活性(3.53±0.63U/gHb)显著低于GSTP1-Ile/Ile基因型的受试者(4.25±1.07U/gHb,P = 0.004),而GSTP1-Val/Val基因型的受试者酶活性最低(2.44±0.67U/gHb)。此外,GSTM10/GSTP1-Ile/Ile携带者的GST活性显著高于遗传GSTM10/GSTP1-Ile/Val或GSTM1*0/GSTP1-Val/Val的受试者。然而,GSTM1无效突变与酶活性降低之间无关联。GSTP1密码子105突变导致中国人红细胞GST活性降低。GSTP1和GSTM1联合无效突变也导致GST活性显著降低。需要进一步研究以探索GSTM1和GSTP1多态性的临床意义。