首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >PET PET imaging of dopamine release in the frontal cortex of manganese‐exposed non‐human primates
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PET PET imaging of dopamine release in the frontal cortex of manganese‐exposed non‐human primates

机译:多巴胺释放的宠物宠物成像在锰暴露的非人类原始化物的前皮质中

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Abstract Humans and non‐human primates exposed to excess levels of manganese (Mn) exhibit deficits in working memory and attention. Frontal cortex and fronto‐striatal networks are implicated in working memory and these circuits rely on dopamine for optimal performance. Here, we aimed to determine if chronic Mn exposure alters in?vivo dopamine release ( DAR ) in the frontal cortex of non‐human primates. We used [ 11 C]‐ FLB 457 positron emission tomography with amphetamine challenge to measure DAR in Cynomolgus macaques . Animals received [ 11 C]‐ FLB 457 positron emission tomography scans with and without amphetamine challenge prior to Mn exposure (baseline), at different time points during the Mn exposure period, and after 10?months of Mn exposure cessation. Four of six Mn‐exposed animals expressed significant impairment of frontal cortex in?vivo DAR relative to baseline. One Mn animal had no change in DAR and another Mn animal expressed increased DAR relative to baseline. In the reversal studies, one Mn‐exposed animal exhibited complete recovery of DAR while the second animal had partial recovery. In both animals, frontal cortex Mn concentrations normalized after 10?months of exposure cessation based on T1‐weighted magnetic resonance imaging. D1‐dopamine receptor (D1R) autoradiography in frontal cortex tissue indicates that Mn animals that experienced cessation of Mn exposure expressed D1R levels that were approximately 50% lower than Mn animals that did not experience cessation of Mn exposure or control animals. The present study provides evidence of Mn‐induced alterations in frontal cortex DAR and D1R that may be associated with working memory and attention deficits observed in Mn‐exposed subjects.
机译:摘要暴露于过量锰(MN)的人和非人类原始化物在工作记忆和注意力中表现出缺陷。正面皮质和前纹版网络在工作存储器中涉及,这些电路依赖于多巴胺以获得最佳性能。在这里,我们旨在确定慢性Mn曝光是否在非人道上的常压性皮层中的α体内多巴胺释放(Dar)。我们使用[11 C] - FLB 457正电子发射断层扫描与amphetamine挑战,以测量达尔在Cynomolgus macaques。收到的动物[11 c] - FLB 457正电子发射断层摄影扫描在Mn暴露期(基线)之前,在Mn暴露时期的不同时间点,10?几个月的Mn曝光停止后,在不同的时间点扫描。六只突出的动物中有四种表达了额外的颅骨皮质的显着损害,相对于基线,达到了基线。一只MN动物在DAR和另一只MN动物表达达到基线时表达了另一种MN的动物。在逆转研究中,一个裸露的动物表现出达到达尔的完全恢复,而第二只动物的部分恢复。在两种动物中,基于T1加权磁共振成像的10次曝光停止后,正面皮质Mn浓度标准化。额外皮层组织中的D1-多巴胺受体(D1R)放射自显影表明,经过经历Mn曝光的灭绝的MN动物表达了比Mn暴露或对照动物停止的Mn动物低约50%的D1R水平。本研究提供了MN诱导的额落Cortex DAR和D1R中的改变的证据,该D1R可以与在MN暴露的受试者中观察到的工作记忆和注意缺陷相关联。

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