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首页> 外文期刊>Psychiatric genetics >Relationship between serotonin transporter gene polymorphisms and platelet serotonin transporter sites among African-American cocaine-dependent individuals and healthy volunteers.
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Relationship between serotonin transporter gene polymorphisms and platelet serotonin transporter sites among African-American cocaine-dependent individuals and healthy volunteers.

机译:非裔可卡因依赖者和健康志愿者中5-羟色胺转运蛋白基因多态性与血小板5-羟色胺转运蛋白位点之间的关系。

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摘要

Alterations in the serotonin transporter (5-HTT) have been implicated in a variety of psychiatric disorders including cocaine dependence. A polymorphism in the promoter region of the serotonin transporter gene (5-HTTLPR) appears to influence the expression of 5-HTT in human cell lines. We investigated whether 5-HTTLPR variants were related to differences in measures of platelet 5-HTT sites in cocaine-dependent patients and healthy volunteers (controls). Polymerase chain reaction-based genotyping of a 44 base pair insertion/deletion polymorphism in 5-HTTLPR was performed in 138 cocaine-dependent African-American subjects and 60 African-American controls. This yielded a short (S) and a long (L) allele. Platelet 5-HTT sites were measured using the tritiated paroxetine binding assay. Relationships of 5-HTTLPR genotypes with Bmax (density of serotonin transporter) and Kd (affinity constant) were examined. Bmax values were significantly lower in cocaine-dependent patients (640 +/- 233) than controls (906 +/-225) (P < 0.001); however, 5-HTTLPR genotype distributions or allele frequencies did not differ between the two groups. There were no significant differences in Bmax between the three genotypes among cocaine-dependent patients (LL = 690 +/- 246, LS = 620 +/- 235, SS = 587 +/- 183; P = 0.14) or controls (LL = 909 +/- 233, LS = 938 +/- 279, SS = 866 +/- 143; P = 0.65). All three genotypes in cocaine-dependent patients showed comparable reductions in Bmax from the corresponding genotypes in controls. Demographic variables, severity of substance use or depression were unrelated to Bmax or 5-HTTLPR genotypes. Although platelet 5-HTT densities are reduced in patients with cocaine dependence compared with healthy volunteers, these genotypic variations in the serotonin transporter do not seem to influence levels of platelet 5-HTT in cocaine-dependent patients or healthy volunteers.
机译:血清素转运蛋白(5-HTT)的改变与多种精神病有关,包括可卡因依赖性。血清素转运蛋白基因(5-HTTLPR)启动子区域的多态性似乎影响5-HTT在人细胞系中的表达。我们调查了5-HTTLPR变异体是否与可卡因依赖患者和健康志愿者(对照组)血小板5-HTT部位的测量值差异有关。在138名可卡因依赖的非裔美国人受试者和60名非裔美国人对照中,对5-HTTLPR中44个碱基对的插入/缺失多态性进行了基于聚合酶链反应的基因分型。这产生了短(S)和长(L)等位基因。使用the化的帕罗西汀结合测定法测量血小板5-HTT位点。检查了5-HTTLPR基因型与Bmax(血清素转运蛋白的密度)和Kd(亲和常数)的关系。可卡因依赖患者(640 +/- 233)的Bmax值显着低于对照组(906 +/- 225)(P <0.001);然而,两组之间的5-HTTLPR基因型分布或等位基因频率没有差异。在可卡因依赖患者(LL = 690 +/- 246,LS = 620 +/- 235,SS = 587 +/- 183; P = 0.14)或对照(LL = 909 +/- 233,LS = 938 +/- 279,SS = 866 +/- 143; P = 0.65)。可卡因依赖患者的所有三种基因型均显示出与对照中相应基因型相比,Bmax的降低程度相当。人口统计学变量,物质使用或抑郁的严重程度与Bmax或5-HTTLPR基因型无关。尽管与健康志愿者相比,可卡因依赖患者的血小板5-HTT密度降低,但血清素转运蛋白的这些基因型变异似乎并不影响可卡因依赖患者或健康志愿者的血小板5-HTT水平。

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