Ferris Craig F, Kulkarni Praveen, Yee Jason R, Nedelman Mark, de Jong Inge E M
Department of Psychology, Center for Translational NeuroImaging, Northeastern UniversityBoston, MA, United States.
Ekam ImagingBoston, MA, United States.
Front Pharmacol. 2017 Jun 12;8:279. doi: 10.3389/fphar.2017.00279. eCollection 2017.
The 5-HT receptor is a promising target for cognitive disorders, in particular for Alzheimer's disease (AD) and other CNS disorders. The high-affinity and selective 5-HT receptor antagonist idalopirdine (Lu AE58054) is currently in development for mild-moderate AD as adjunct therapy to acetylcholinesterase inhibitors (AChEIs). We studied the effects of idalopirdine alone and in combination with the AChEI donepezil on brain activity using BOLD (Blood Oxygen Level Dependent) functional magnetic resonance imaging (fMRI) in the awake rat. Idalopirdine (2 mg/kg, i.v.) alone had a modest effect on brain activity, resulting in activation of eight brain regions at the peak response. Of these, the cholinergic diagonal band of Broca, the infralimbic cortex, the ventral pallidum, the nucleus accumbens shell, and the magnocellular preoptic area were shared with the effects of donepezil (0.3 mg/kg, i.v.). Donepezil alone activated 19 brain regions at the peak response, including several cortical regions, areas of the septo-hippocampal system and the serotonergic raphe nucleus. When idalopirdine and donepezil were combined, there was a robust stimulation pattern with activation of 36 brain regions spread across the extended-amygdala-, striato-pallidal, and septo-hippocampal networks as well as the cholinergic system. These findings indicate that, whilst idalopirdine and donepezil recruit a number of overlapping regions including one of the forebrain cholinergic nuclei, the synergistic effect of both compounds extends beyond the cholinergic system and the effects of donepezil alone toward recruitment of multiple neural circuits and neurotransmitter systems. These data provide new insight into the mechanisms via which idalopirdine might improve cognition in donepezil-treated AD patients.
5-羟色胺受体是认知障碍尤其是阿尔茨海默病(AD)和其他中枢神经系统疾病的一个有前景的靶点。高亲和力和选择性5-羟色胺受体拮抗剂依达拉奉(Lu AE58054)目前正在开发用于轻度至中度AD,作为乙酰胆碱酯酶抑制剂(AChEIs)的辅助治疗。我们使用清醒大鼠的血氧水平依赖(BOLD)功能磁共振成像(fMRI)研究了依达拉奉单独使用以及与AChEI多奈哌齐联合使用对大脑活动的影响。单独静脉注射依达拉奉(2 mg/kg)对大脑活动有适度影响,在峰值反应时导致八个脑区激活。其中,布罗卡胆碱能斜带、边缘下皮质、腹侧苍白球、伏隔核壳和大细胞视前区与多奈哌齐(静脉注射0.3 mg/kg)的作用有重叠。单独使用多奈哌齐在峰值反应时激活了19个脑区,包括几个皮质区域、隔-海马系统区域和5-羟色胺能中缝核。当依达拉奉和多奈哌齐联合使用时,出现了强烈的刺激模式,激活了36个脑区,分布在扩展杏仁核、纹状体-苍白球和隔-海马网络以及胆碱能系统。这些发现表明,虽然依达拉奉和多奈哌齐募集了许多重叠区域,包括一个前脑胆碱能核,但两种化合物的协同作用超出了胆碱能系统以及单独使用多奈哌齐的作用,可募集多个神经回路和神经递质系统。这些数据为依达拉奉可能改善多奈哌齐治疗的AD患者认知的机制提供了新的见解。