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印度尼西亚爪哇族人群中的丁酰胆碱酯酶和C5+变体

Butyrylcholinesterase and C5+ variant in a Javanese ethnic group in Indonesia.

作者信息

Suyatna F D, Setiabudy R, Herwana E

机构信息

Department of Pharmacology, Medical Faculty, University of Indonesia, Jakarta, Indonesia.

出版信息

Int J Clin Pharmacol Ther. 2000 Jul;38(7):339-44. doi: 10.5414/cpp38339.

Abstract

OBJECTIVE

This study was designed to investigate the butyrylcholinesterase (BChE) and C5 variant phenotypes in a Javanese ethnic group in Indonesia. BLOOD-DONORS, MATERIALS AND METHODS: Random blood samples from a Javanese ethnic group were obtained from the Indonesian Red Cross Service. The donors were 40.09 +/- 9.53 years old, consisting of 358 (89.45%) males and 42 females (10.55%). The plasma content of BChE was determined spectrophotometrically using benzoylcholine as substrate, and phenotyping of BChE was performed using the inhibitors 10 microM dibucaine and 50 microM sodium fluoride. Phenotyping of the C5+ variant was carried out by means of polyacrylamide gel electrophoresis using a 7.5% (w/v) acrylamide slab gel and a 3% (w/v) acrylamide stacking gel, and stained with fast red azo dye.

RESULTS

The results show that of 398 samples studied, the average activities of BChE are 1.00 +/- 0.22 U/ml. 377 individuals (94.72%) show normal activities, whereas 21 individuals (5.78%) are below normal (< 0.690 U/ml). The mean +/- SD of dibucaine number (DN) is 83 +/- 5 and the fluoride number (FN) is 66 +/- 6. From this population we identified one individual with UA phenotype (total activity: 0.310 U/ml, DN: 62, and FN: 50). The frequency of C5+ variant in the population as detected by acrylamide electrophoresis is 21%.

CONCLUSION

Our data indicate that the atypical allele of BChE is rare and that the C5+ variant is detected in high frequency in the ethnic Javanese of Indonesia.

摘要

目的

本研究旨在调查印度尼西亚爪哇族人群中的丁酰胆碱酯酶(BChE)和C5变异表型。

献血者、材料与方法:从印度尼西亚红十字会服务处获取爪哇族人群的随机血样。献血者年龄为40.09±9.53岁,其中男性358名(89.45%),女性42名(10.55%)。以苯甲酰胆碱为底物,采用分光光度法测定血浆中BChE的含量,并使用10微摩尔/升的地布卡因和50微摩尔/升的氟化钠抑制剂对BChE进行表型分析。采用7.5%(w/v)丙烯酰胺平板凝胶和3%(w/v)丙烯酰胺堆积凝胶进行聚丙烯酰胺凝胶电泳对C5+变异体进行表型分析,并用固红偶氮染料染色。

结果

结果显示,在所研究的398个样本中,BChE的平均活性为1.00±0.22单位/毫升。377名个体(94.72%)活性正常,而21名个体(5.78%)活性低于正常水平(<0.690单位/毫升)。地布卡因值(DN)的平均值±标准差为83±5,氟化物值(FN)为66±6。从该人群中我们鉴定出1名具有UA表型的个体(总活性:0.310单位/毫升,DN:62,FN:50)。通过丙烯酰胺电泳检测到该人群中C5+变异体的频率为21%。

结论

我们的数据表明,BChE的非典型等位基因罕见,而在印度尼西亚爪哇族人群中C5+变异体的检测频率较高。

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