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()-CE-123 对中皮层边缘多巴胺系统的神经生理和神经化学作用。

Neurophysiological and Neurochemical Effects of the Putative Cognitive Enhancer ()-CE-123 on Mesocorticolimbic Dopamine System.

机构信息

Department of Biomedical Sciences, Division of Neuroscience and Clinical Pharmacology, University of Cagliari, 09042 Monserrato, Italy.

Department of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, 1010 Vienna, Austria.

出版信息

Biomolecules. 2020 May 18;10(5):779. doi: 10.3390/biom10050779.

DOI:10.3390/biom10050779
PMID:32443397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7277835/
Abstract

Treatments for cognitive impairments associated with neuropsychiatric disorders, such as attention deficit hyperactivity disorder or narcolepsy, aim at modulating extracellular dopamine levels in the brain. CE-123 (5-((benzhydrylsulfinyl)methyl) thiazole) is a novel modafinil analog with improved specificity and efficacy for dopamine transporter inhibition that improves cognitive and motivational processes in experimental animals. We studied the neuropharmacological and behavioral effects of the -enantiomer of CE-123 (()-CE-123) and -modafinil in cognitive- and reward-related brain areas of adult male rats. In vivo single unit recordings in anesthetized animals showed that ()-CE-123, but not -modafinil, dose-dependently (1.25 to 10 mg/kg i.v.) reduced firing of pyramidal neurons in the infralimbic/prelimbic (IL/PrL) cortex. Neither compound the affected firing activity of ventral tegmental area dopamine cells. In freely moving animals, ()-CE-123 (10 mg/kg i.p.) increased extracellular dopamine levels in the IL/PrL, with different patterns when compared to -modafinil (10 mg/kg i.p.); in the nucleus accumbens shell, a low and transitory increase of dopamine was observed only after ()-CE-123. Neither ()-CE-123 nor -modafinil initiated the emission of 50-kHz ultrasonic vocalizations, a behavioral marker of positive affect and drug-mediated reward. Our data support previous reports of the procognitive effects of ()-CE-123, and show a minor impact on reward-related dopaminergic areas.

摘要

治疗与神经精神障碍相关的认知障碍的方法,例如注意缺陷多动障碍或发作性睡病,旨在调节大脑中的细胞外多巴胺水平。CE-123(5-((苯并[d]硫基)甲基)噻唑)是一种新型莫达非尼类似物,对多巴胺转运体的抑制具有更高的特异性和功效,可改善实验动物的认知和动机过程。我们研究了 CE-123 的 -对映异构体(()-CE-123)和 -莫达非尼在成年雄性大鼠认知和奖励相关脑区的神经药理学和行为效应。在麻醉动物的体内单细胞记录中,结果表明()-CE-123 而非 -莫达非尼(1.25 至 10 mg/kg 静脉注射)剂量依赖性地降低了边缘前皮质(IL/PrL)中锥体神经元的放电。两种化合物均未影响腹侧被盖区多巴胺细胞的放电活动。在自由活动的动物中,()-CE-123(10 mg/kg 腹腔注射)增加了 IL/PrL 中的细胞外多巴胺水平,与 -莫达非尼(10 mg/kg 腹腔注射)相比表现出不同的模式;在伏隔核壳中,仅在()-CE-123 后观察到多巴胺的低且短暂增加。()-CE-123 和 -莫达非尼均未引发 50-kHz 超声发声,这是积极影响和药物介导的奖励的行为标志物。我们的数据支持了()-CE-123 的促认知作用的先前报道,并表明对奖励相关多巴胺能区域的影响较小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/18a7e2dc104f/biomolecules-10-00779-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/1b36aa154cb6/biomolecules-10-00779-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/ca505fcabdfc/biomolecules-10-00779-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/896e8a6fd5ce/biomolecules-10-00779-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/673773f70984/biomolecules-10-00779-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/18a7e2dc104f/biomolecules-10-00779-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/1b36aa154cb6/biomolecules-10-00779-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/ca505fcabdfc/biomolecules-10-00779-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/896e8a6fd5ce/biomolecules-10-00779-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/673773f70984/biomolecules-10-00779-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c063/7277835/18a7e2dc104f/biomolecules-10-00779-g005.jpg

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