Svoboda Jan, Popelikova Anna, Stuchlik Ales
Institute of Physiology of the Czech Academy of Sciences, Prague, Czechia.
Front Psychiatry. 2017 Nov 9;8:215. doi: 10.3389/fpsyt.2017.00215. eCollection 2017.
Muscarinic acetylcholine receptors (mAChRs) have been found to regulate many diverse functions, ranging from motivation and feeding to spatial navigation, an important and widely studied type of cognitive behavior. Systemic administration of non-selective antagonists of mAChRs, such as scopolamine or atropine, have been found to have adverse effects on a vast majority of place navigation tasks. However, many of these results may be potentially confounded by disruptions of functions other than spatial learning and memory. Although studies with selective antimuscarinics point to mutually opposite effects of M1 and M2 receptors, their particular contribution to spatial cognition is still poorly understood, partly due to a lack of truly selective agents. Furthermore, constitutive knock-outs do not always support results from selective antagonists. For modeling impaired spatial cognition, the scopolamine-induced amnesia model still maintains some limited validity, but there is an apparent need for more targeted approaches such as local intracerebral administration of antagonists, as well as novel techniques such as optogenetics focused on cholinergic neurons and chemogenetics aimed at cells expressing metabotropic mAChRs.
已发现毒蕈碱型乙酰胆碱受体(mAChRs)可调节多种不同功能,从动机和摄食到空间导航,空间导航是一种重要且被广泛研究的认知行为类型。已发现全身给予mAChRs的非选择性拮抗剂,如东莨菪碱或阿托品,会对绝大多数位置导航任务产生不利影响。然而,许多这些结果可能会因空间学习和记忆以外的功能破坏而受到潜在混淆。尽管使用选择性抗毒蕈碱药物的研究表明M1和M2受体具有相互相反的作用,但它们对空间认知的具体贡献仍知之甚少,部分原因是缺乏真正的选择性药物。此外,组成型基因敲除并不总是支持选择性拮抗剂的结果。对于模拟受损的空间认知,东莨菪碱诱导的失忆模型仍具有一定的有限有效性,但显然需要更具针对性的方法,如局部脑内给予拮抗剂,以及诸如针对胆碱能神经元的光遗传学和针对表达代谢型mAChRs的细胞的化学遗传学等新技术。