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吸烟者血液淋巴细胞中多巴胺D3受体表达降低与每日吸烟量呈负相关:吸烟者多巴胺能改变的外周关联。

Reduced dopamine D3 receptor expression in blood lymphocytes of smokers is negatively correlated with daily number of smoked cigarettes: a peripheral correlate of dopaminergic alterations in smokers.

作者信息

Czermak Christoph, Lehofer Michael, Wagner Elke M, Prietl Barbara, Gorkiewicz Gregor, Lemonis Leonidas, Rohrhofer Alfred, Legl Thomas, Schauenstein Konrad, Liebmann Peter M

机构信息

Institute of Pathophysiology, University of Graz, Austria.

出版信息

Nicotine Tob Res. 2004 Feb;6(1):49-54. doi: 10.1080/14622200310001656858.

Abstract

The mesolimbic dopaminergic system is known to mediate rewarding effects of nicotine administration, and dysfunctions of this system may underlie failure to stop cigarette smoking. Expression of dopamine receptors in peripheral blood lymphocytes (PBLs) has been indicated as a peripheral correlate of brain status. Dopamine receptor D(3) (DRD3) and D(4) (DRD4) mRNA expression in PBLs was measured by real-time polymerase chain reaction in smokers (n=26) and former smokers (n=14), compared with nonsmoking control subjects (n=35). A significant (p=.032, Bonferroni corrected) 30% reduction of DRD3 mRNA expression in PBLs was found in smokers but not former smokers in comparison with controls. DRD3 mRNA expression in PBLs in smokers but not former smokers was negatively correlated with daily number of cigarettes consumed (Pearson correlation coefficient r=-.54, p=.005). These data suggest a selective inhibiting effect of smoking on DRD3 mRNA expression and, with the known involvement of DRD3 in reward mediation, indicates a vicious-cycle explanation for the motivation for continued smoking.

摘要

中脑边缘多巴胺能系统已知可介导尼古丁给药的奖赏效应,该系统功能障碍可能是戒烟失败的原因。外周血淋巴细胞(PBLs)中多巴胺受体的表达已被表明是脑状态的外周相关指标。通过实时聚合酶链反应测量吸烟者(n = 26)和既往吸烟者(n = 14)外周血淋巴细胞中多巴胺受体D(3)(DRD3)和D(4)(DRD4)mRNA的表达,并与非吸烟对照受试者(n = 35)进行比较。与对照组相比,吸烟者外周血淋巴细胞中DRD3 mRNA表达显著降低(p = 0.032,经Bonferroni校正)30%,而既往吸烟者未出现此现象。吸烟者而非既往吸烟者外周血淋巴细胞中DRD3 mRNA表达与每日吸烟量呈负相关(Pearson相关系数r = -0.54,p = 0.005)。这些数据表明吸烟对DRD3 mRNA表达具有选择性抑制作用,并且鉴于DRD3已知参与奖赏调节,这为持续吸烟的动机提供了一种恶性循环的解释。

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