Grisel J E, Belknap J K, O'Toole L A, Helms M L, Wenger C D, Crabbe J C
Research Service, Veterans Affairs Medical Center, Portland, OR 97201, USA.
J Neurosci. 1997 Jan 15;17(2):745-54. doi: 10.1523/JNEUROSCI.17-02-00745.1997.
Individual differences in most behavioral and pharmacological responses to abused drugs are dependent on both genetic and environmental factors. The genetic influences on the complex phenotypes related to drug abuse have been difficult to study using classical genetic analyses. Quantitative trait locus (QTL) mapping is a method that has been used successfully to examine genetic contributions to some of these traits by correlating allelic variation in polymorphic genetic markers of known chromosomal location with variation in drug-response phenotypes. We evaluated several behavioral responses to multiple doses of methamphetamine (METH) in C57BL/6J (B6), DBA/2J (D2), and 25 of their recombinant inbred (BXD RI) strains. Stereotyped chewing, horizontal home cage activity, and changes in body temperature after 0, 4, 8, or 16 mg/kg METH, as well as stereotyped climbing behavior after 16 mg/kg METH, were examined. Associations (p < 0.01) between METH sensitivity and allelic status at multiple microsatellite genetic markers were subsequently determined for each response. QTLs were provisionally identified for each phenotype, some unique to a particular behavior and others that appeared to influence multiple phenotypes. Candidate genes suggested by these analyses included several that mapped near genes relevant for the neurotransmitters acetylcholine and glutamate. The locations of QTLs provisionally identified by this analysis were compared with QTLs hypothesized in other studies to influence methamphetamine- and cocaine-related phenotypes. In several instances, QTLs appeared to overlap, which is consistent with idea that common neural substrates underlie some responses to psychostimulants.
大多数对滥用药物的行为和药理学反应的个体差异取决于遗传和环境因素。使用经典遗传分析方法很难研究遗传因素对与药物滥用相关的复杂表型的影响。数量性状基因座(QTL)定位是一种已成功用于通过将已知染色体位置的多态性遗传标记中的等位基因变异与药物反应表型的变异相关联,来研究这些性状中某些性状的遗传贡献的方法。我们评估了C57BL/6J(B6)、DBA/2J(D2)及其25个重组近交(BXD RI)品系对多剂量甲基苯丙胺(METH)的几种行为反应。检测了0、4、8或16mg/kg METH给药后刻板咀嚼、水平笼内活动和体温变化,以及16mg/kg METH给药后的刻板攀爬行为。随后确定了每种反应在多个微卫星遗传标记处METH敏感性与等位基因状态之间的关联(p<0.01)。初步确定了每种表型的QTL,有些QTL是特定行为所特有的,而另一些则似乎影响多种表型。这些分析提示的候选基因包括几个位于与神经递质乙酰胆碱和谷氨酸相关基因附近的基因。将该分析初步确定的QTL位置与其他研究中假设的影响甲基苯丙胺和可卡因相关表型的QTL进行了比较。在几个实例中,QTL似乎重叠,这与某些对精神兴奋剂的反应具有共同神经底物的观点一致。