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大麻素受体基因(CNR1)在德国静脉注射吸毒者中未受影响。

The cannabinoid receptor gene (CNR1) is not affected in German i.v. drug users.

作者信息

Heller D., Schneider U., Seifert J., Cimander K. F., Stuhrmann M.

机构信息

Institute of Human Genetics, Medical School, D-30625 Hannover, Germany.

出版信息

Addict Biol. 2001 Apr;6(2):183-187. doi: 10.1080/13556210020040271.

Abstract

The aim of the study was to investigate a possible contribution of the cannabinoid receptor gene (CNR1) to the development of i.v. drug addiction. Allele and genotype frequencies of a previously associated flanking triplet repeat polymorphism were compared between patients and controls, and the whole coding region of the CNR1 gene of all patients were screened for presence of mutations. The study took place at the Addiction Treatment Unit of the Medical School Hannover, and two outpatients' departments in Hannover, Germany. Forty German unrelated opioid addicts (27 males and 13 females; mean age 37.9 years; range 16-53 years), took part, all of them satisfying ICD-10 and DSM-IV diagnostic criteria for opioid dependence and 81 age- and sex-matched controls (German blood donors). Measurements used were lengths of alleles, genotyping and single strand conformation polymorphism (SSCP) analysis. Neither the >/= 5 alleles of the extragenic triplet repeat (AAT) marker nor the alleles of an intragenic biallelic CNR1 polymorphism (1359G/A) were associated with i.v. drug use in our study group. In addition, we did not detect any sequence variation within the CNR1 gene which could confer susceptibility to i.v. drug abuse. In contrast to previous investigations, we found no evidence for an involvement of the CNR1 gene in i.v. drug addiction.

摘要

该研究的目的是调查大麻素受体基因(CNR1)对静脉注射药物成瘾发展的可能作用。比较了患者和对照组之间先前相关的侧翼三联体重复多态性的等位基因和基因型频率,并对所有患者的CNR1基因的整个编码区进行了突变筛查。该研究在汉诺威医学院的成瘾治疗科以及德国汉诺威的两个门诊部进行。40名德国无亲属关系的阿片类药物成瘾者(27名男性和13名女性;平均年龄37.9岁;范围16 - 53岁)参与了研究,他们均符合ICD - 10和DSM - IV关于阿片类物质依赖的诊断标准,还有81名年龄和性别匹配的对照者(德国献血者)。所采用的测量方法包括等位基因长度、基因分型和单链构象多态性(SSCP)分析。在我们的研究组中,基因外三联体重复(AAT)标记的≥5个等位基因以及基因内双等位基因CNR1多态性(1359G/A)的等位基因均与静脉注射药物使用无关。此外,我们未在CNR1基因内检测到任何可能导致静脉注射药物滥用易感性的序列变异。与先前的研究相反,我们没有发现CNR1基因参与静脉注射药物成瘾的证据。

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