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线粒体DNA突变与氨基糖甙类抗生素致聋的关系
引用本文:张丽珊,陆明华,黄鹰,周哓雷,邱定红,王为未. 线粒体DNA突变与氨基糖甙类抗生素致聋的关系[J]. 中华医学遗传学杂志, 1999, 16(3): 138-140
作者姓名:张丽珊  陆明华  黄鹰  周哓雷  邱定红  王为未
作者单位:1. 210009,南京铁道医学院生物学教研室
2. 上海肿瘤研究所
摘    要:目的探讨线粒体DNA突变与氨基糖甙类抗生素致聋的关系。方法应用PCR-BsmAI酶切及PCR产物直接银染测序,对48例氨基糖甙类抗生素致聋散发患者外周血标本的线粒体DNA进行分析。结果发现6例患者线粒体DNA12SrRNA基因核苷酸第1555位点发生了A→G突变。结论氨基糖甙类抗生素致聋有明显的个体差异,带有1555G的个体对氨基糖甙类抗生素的耳毒作用有高度易感性。

关 键 词:线粒体DNA  突变  氨基糖甙类抗生素致聋

The relation between mitochondrial DNA mutation and aminoglycoside antibiotics-induced deafness
ZHANG Lishan,LU Minghua,HUANG Ying,ZHOU Xiaolei,QIU Dinghong,WANG Weiwei. The relation between mitochondrial DNA mutation and aminoglycoside antibiotics-induced deafness[J]. Chinese journal of medical genetics, 1999, 16(3): 138-140
Authors:ZHANG Lishan  LU Minghua  HUANG Ying  ZHOU Xiaolei  QIU Dinghong  WANG Weiwei
Affiliation:Department of Biology, Nanjing Railway Medical College, Nanjing, 210009 P. R. China. LishanZh@jlonline.com
Abstract:Objective To investigate the relation between mitochondrial DNA mutation and aminoglycoside antibioticsinduced deafness. Methods Mitochondrial DNA (mtDNA) of peripheral blood from 48 sporadic cases was analysed using PCRBsmAI digestion and PCRdirect DNA silver sequencing. Results Six of 48 sporadic patients had A to G mutation in 12S rRNA gene of mtDNA at nucleotide 1555.THZConclusion The results suggest that mtDNA 1555G mutation is related to the occurring of aminoglycoside antibioticsinduced deafness which can cause genetic susceptibility to aminoglycoside antibotics ototoxicity.
Keywords:Mitochondrial DNAMutationAminoglycoside antibioticsinduced deafness  
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