Koshy Cherian Ajeesh, Tronson Natalie C, Parikh Vinay, Kucinski Aaron, Blakely Randy D, Sarter Martin
Department of Psychology and Neuroscience Program.
Department of Psychology.
Behav Neurosci. 2019 Aug;133(4):448-459. doi: 10.1037/bne0000310. Epub 2019 Mar 21.
Previous research emphasized the impact of traumatic brain injury on cholinergic systems and associated cognitive functions. Here we addressed the converse question: Because of the available evidence indicating cognitive and neuronal vulnerabilities in humans expressing low-capacity cholinergic systems or with declining cholinergic systems, do injuries cause more severe cognitive decline in such subjects, and what cholinergic mechanisms contribute to such vulnerability? Using mice heterozygous for the choline transporter (CHT+/- mice) as a model for a limited cholinergic capacity, we investigated the cognitive and neuronal consequences of repeated, mild concussion injuries (rmCc). After five rmCc, and compared with wild type (WT) mice, CHT+/- mice exhibited severe and lasting impairments in sustained attention performance, consistent with effects of cholinergic losses on attention. However, rmCc did not affect the integrity of neuronal cell bodies and did not alter the density of cortical synapses. As a cellular mechanism potentially responsible for the attentional impairment in CHT+/- mice, we found that rmCc nearly completely attenuated performance-associated, CHT-mediated choline transport. These results predict that subjects with an already vulnerable cholinergic system will experience severe and lasting cognitive-cholinergic effects after even relatively mild injuries. If confirmed in humans, such subjects may be excluded from, or receive special protection against, activities involving injury risk. Moreover, the treatment and long-term outcome of traumatic brain injuries may benefit from determining the status of cholinergic systems and associated cognitive functions. (PsycINFO Database Record (c) 2019 APA, all rights reserved).
先前的研究强调了创伤性脑损伤对胆碱能系统及相关认知功能的影响。在此,我们探讨相反的问题:鉴于现有证据表明,表达低容量胆碱能系统或胆碱能系统功能衰退的人类存在认知和神经元易损性,那么损伤是否会在此类个体中导致更严重的认知衰退,以及哪些胆碱能机制导致了这种易损性?我们使用胆碱转运体杂合子小鼠(CHT+/-小鼠)作为胆碱能容量有限的模型,研究了反复轻度脑震荡损伤(rmCc)的认知和神经元后果。经过五次rmCc后,与野生型(WT)小鼠相比,CHT+/-小鼠在持续注意力表现上出现了严重且持久的损伤,这与胆碱能丧失对注意力的影响一致。然而,rmCc并未影响神经元细胞体的完整性,也未改变皮质突触的密度。作为CHT+/-小鼠注意力损伤潜在的细胞机制,我们发现rmCc几乎完全减弱了与表现相关的、CHT介导的胆碱转运。这些结果预测,胆碱能系统本就脆弱的个体,即使遭受相对较轻的损伤,也会经历严重且持久的认知 - 胆碱能效应。如果在人类中得到证实,此类个体可能会被排除在有受伤风险的活动之外,或在这些活动中接受特殊保护。此外,创伤性脑损伤的治疗和长期预后可能会受益于确定胆碱能系统的状态及相关认知功能。(PsycINFO数据库记录(c)2019美国心理学会,保留所有权利)