Eickhoff Sofia, Franzen Leon, Korda Alexandra, Rogg Helena, Trulley Valerie-Noelle, Borgwardt Stefan, Avram Mihai
Translational Psychiatry, Department of Psychiatry and Psychotherapy, University of Lübeck, Lübeck, Germany.
Front Psychiatry. 2022 Jul 6;13:909961. doi: 10.3389/fpsyt.2022.909961. eCollection 2022.
The basal forebrain cholinergic nuclei (BFCN) provide the main cholinergic input to prefrontal cortices, the hippocampi, and amygdala. These structures are highly relevant for the regulation and maintenance of many cognitive functions, such as attention and memory. neuroimaging studies reported alterations of the cholinergic system in psychotic disorders. Particularly, a downregulation of nicotinic and muscarinic acetylcholine receptors has been found. Crucially, such alterations in neurotransmission have been associated with cognitive impairments and positive and negative symptoms. Recent pharmacological studies support these findings, as they demonstrated an association between the manipulation of cholinergic transmission and an attenuation in symptom severity. Targeting acetylcholine receptors has therefore become a focus for the development of novel psychopharmacological drugs. However, many open questions remain. For instance, it remains elusive what causes such alterations in neurotransmission. While evidence supports the idea that BFCN structural integrity is altered in schizophrenia, it remains to be determined whether this is also present in other psychotic disorders. Furthermore, it is unclear when throughout the course of the disorder these alterations make their appearance and whether they reflect changes in the BFCN alone or rather aberrant interactions between the BFCN and other brain areas. In this review, the specific role of the BFCN and their projections are discussed from a neuroimaging perspective and with a focus on psychotic disorders alongside future directions. These directions set the stage for the development of new treatment targets for psychotic disorders.
基底前脑胆碱能核团(BFCN)为前额叶皮质、海马体和杏仁核提供主要的胆碱能输入。这些结构与许多认知功能的调节和维持高度相关,如注意力和记忆。神经影像学研究报告了精神障碍中胆碱能系统的改变。特别是,已发现烟碱型和毒蕈碱型乙酰胆碱受体下调。至关重要的是,这种神经传递的改变与认知障碍以及阳性和阴性症状有关。最近的药理学研究支持了这些发现,因为它们证明了胆碱能传递的操纵与症状严重程度的减轻之间存在关联。因此,靶向乙酰胆碱受体已成为新型精神药物开发的重点。然而,许多问题仍然悬而未决。例如,神经传递发生这种改变的原因仍然难以捉摸。虽然有证据支持精神分裂症中BFCN结构完整性发生改变的观点,但在其他精神障碍中是否也存在这种情况仍有待确定。此外,尚不清楚在疾病过程中的何时会出现这些改变,以及它们是仅反映BFCN的变化还是反映BFCN与其他脑区之间的异常相互作用。在这篇综述中,从神经影像学角度并聚焦于精神障碍以及未来方向,讨论了BFCN及其投射的具体作用。这些方向为精神障碍新治疗靶点的开发奠定了基础。