Gibbons Andrew, Dean Brian
The Florey Institute of Neuroscience and Mental Health, 30 Royal Parade, Parkville, Victoria 3052, Australia.
Curr Pharm Des. 2016;22(14):2124-33. doi: 10.2174/1381612822666160127114010.
Cognitive deficits are amongst the most socially debilitating and least effectively treated symptoms of schizophrenia. The cholinergic system is a promising target for the design of novel drugs that can more effectively treat these symptoms.
We review the literature supporting the dysfunction of the cholinergic system in schizophrenia, discuss the preclinical and clinical data showing that modulating the cholinergic system could improve the symptoms of schizophrenia and review the main pharmacological strategies being investigated to treat cholinergic dysfunction in schizophrenia.
Post-mortem and neuroimaging studies suggest there are widespread reductions in cholinergic receptor signalling in the cortex as well as subcortical regions, such as the hippocampus and striatum, in individuals with schizophrenia. Potential cholinergic drug targets are being pursued to increase receptor function. These include inhibiting the activity of the enzyme acetylcholinesterase to increase synaptic acetylcholine levels, and increasing the nicotinic receptor and muscarinic receptor activity with agonists or positive allosteric modulators.
Amongst the most promising drug targets for treating schizophrenia are the α7 nicotinic receptor and the CHRM1 and CHRM4 muscarinic receptors. The recent development of allosteric modulators that selectively target these receptors offers the potential to more effectively treat the symptoms of schizophrenia.
认知缺陷是精神分裂症中最具社会危害性且治疗效果最差的症状之一。胆碱能系统是设计能够更有效治疗这些症状的新型药物的一个有前景的靶点。
我们回顾了支持精神分裂症中胆碱能系统功能障碍的文献,讨论了临床前和临床数据,这些数据表明调节胆碱能系统可改善精神分裂症症状,并回顾了正在研究的治疗精神分裂症胆碱能功能障碍的主要药理学策略。
尸检和神经影像学研究表明,精神分裂症患者的皮质以及海马体和纹状体等皮质下区域的胆碱能受体信号广泛减少。正在寻找潜在的胆碱能药物靶点以增强受体功能。这些包括抑制乙酰胆碱酯酶的活性以增加突触乙酰胆碱水平,以及用激动剂或正变构调节剂增加烟碱受体和毒蕈碱受体的活性。
治疗精神分裂症最有前景的药物靶点包括α7烟碱受体以及毒蕈碱受体CHRM1和CHRM4。最近开发的选择性靶向这些受体的变构调节剂为更有效治疗精神分裂症症状提供了潜力。