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首页> 外文期刊>Journal of Neural Transmission >Nicotinic acetylcholine receptor expression on B-lymphoblasts of healthy versus schizophrenic subjects stratified for smoking: [3H]-nicotine binding is decreased in schizophrenia and correlates with negative symptoms
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Nicotinic acetylcholine receptor expression on B-lymphoblasts of healthy versus schizophrenic subjects stratified for smoking: [3H]-nicotine binding is decreased in schizophrenia and correlates with negative symptoms

机译:分层吸烟的健康人群与精神分裂症患者B淋巴细胞中烟碱乙酰胆碱受体的表达:[3 H]-尼古丁在精神分裂症中的结合减少,并与阴性症状相关

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摘要

Heavy smoking and schizophrenia are diversely associated with nicotinic acetylcholine receptor expression, as was shown for brain and lymphocytes. Most studies so far have not systematically differentiated between schizophrenia smokers and non-smokers and were confined either to in vivo or post-mortem study approaches. In order to avoid variable in vivo influences or post-mortem bias, we used stably transformed B-lymphoblast cultures derived from healthy and schizophrenia subjects stratified for smoking versus non-smoking in order to differentiate these clinical conditions with regard to nicotinic acetylcholine receptor expression and regulation. Receptor quantities were measured using [3H]-nicotine and [3H]-epibatidine binding. At baseline, [3H]-nicotine binding was not statistically different between healthy smokers and never-smokers (1.59 ± 0.73 vs. 1.26 ± 0.91 fmol/106 cells), while it was reduced in schizophrenia smokers compared to healthy smokers (1.05 ± 0.69 fmol vs. 1.44 ± 0.84/106 cells, P = 0.01). In schizophrenia, baseline [3H]-nicotine correlated inversely with higher PANSS negative subscale scores. After long-term nicotine incubation (1 μM), [3H]-nicotine binding increased in the group of schizophrenia smokers only (from 1.05 ± 0.69 to 1.54 ± 0.77 fmol/106 cells, P = 0.013), while [3H]-epibatidine binding decreased in this group (4.52 ± 1.52 to 3.82 ± 1.38 fmol/106 cells, P = 0.038). Our data are in further support of a decrease of nicotinic acetylcholine receptor expression in schizophrenia linked to negative psychotic symptoms, which may be counter-regulated by nicotine exposure.
机译:如脑部和淋巴细胞所示,大量吸烟和精神分裂症与烟碱型乙酰胆碱受体的表达不同。迄今为止,大多数研究还没有系统地区分精神分裂症吸烟者和非吸烟者,并且仅限于体内或验尸研究方法。为了避免可变的体内影响或验尸偏倚,我们使用了来自健康和精神分裂症受试者的稳定转化的B淋巴母细胞培养物,将其分层划分为吸烟与不吸烟,以针对烟碱型乙酰胆碱受体表达和规。使用[3 H]-烟碱和[3 ]-依巴替丁结合测量受体的量。在基线时,[3 H]-烟碱结合在健康吸烟者和从不吸烟者之间无统计学差异(1.59±0.73 vs. 1.26±0.91 fmol / 106 细胞),而在精神分裂症中降低吸烟者与健康吸烟者相比(1.05±0.69 fmol对1.44±0.84 / 106 细胞,P = 0.01)。在精神分裂症中,基线[3 H]-烟碱与PANSS负子量表得分较高成反比。长期尼古丁孵育(1μM)后,仅精神分裂症吸烟者组[3H]-烟碱结合增加(从1.05±0.69增至1.54±0.77 fmol / 106细胞,P = 0.013),而[3 H]-依巴替丁的结合减少(4.52±1.52至3.82±1.38 fmol / 106 细胞,P = 0.038)。我们的数据进一步支持精神分裂症中与阴性精神病症状有关的烟碱型乙酰胆碱受体表达的减少,这可能是由于尼古丁暴露所引起的。

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