Wu M, Shanabrough M, Leranth C, Alreja M
Departments of Psychiatry, Obstetrics and Gynecology, and Neurobiology, Yale University School of Medicine and the Ribicoff Research Facilities, Connecticut Mental Health Center, New Haven, Connecticut 06508, USA.
J Neurosci. 2000 May 15;20(10):3900-8. doi: 10.1523/JNEUROSCI.20-10-03900.2000.
The medial septum/diagonal band (MSDB), which gives rise to the septohippocampal pathway, is a critical locus for the mnemonic effects of muscarinic drugs. Infusion of muscarinic cholinergic agonists into the MSDB enhance learning and memory processes both in young and aged rats and produce a continuous theta rhythm in the hippocampus. Intraseptal muscarinic agonists also alleviate the amnesic syndrome produced by systemic administration of muscarinic receptor antagonists. It has been presumed, but not proven, that the cellular mechanisms underlying the effects of muscarinic agonists in the MSDB involve an excitation of septohippocampal cholinergic neurons and a subsequent increase in acetylcholine (ACh) release in the hippocampus. Using a novel fluorescent labeling technique to selectively visualize live septohippocampal cholinergic neurons in rat brain slices, we have found that muscarinic agonists do not excite septohippocampal cholinergic neurons, instead they inhibit a subpopulation of cholinergic neurons. In contrast, unlabeled neurons, confirmed to be noncholinergic, septohippocampal GABA-type neurons using retrograde marking and double-labeling techniques, are profoundly excited by muscarine. Thus, the cognition-enhancing effects of muscarinic drugs in the MSDB cannot be attributed to an increase in hippocampal ACh release. Instead, disinhibitory mechanisms, caused by increased impulse flow in the septohippocampal GABAergic pathway, may underlie the cognition-enhancing effects of muscarinic agonists.
内侧隔区/斜角带(MSDB)发出隔海马通路,是毒蕈碱类药物产生记忆效应的关键部位。向MSDB内注入毒蕈碱胆碱能激动剂可增强年轻和老年大鼠的学习和记忆过程,并在海马体中产生持续的θ节律。隔区内注入毒蕈碱激动剂还可减轻全身给予毒蕈碱受体拮抗剂所产生的失忆综合征。据推测,但未经证实,毒蕈碱激动剂在MSDB中发挥作用的细胞机制涉及隔海马胆碱能神经元的兴奋以及随后海马体中乙酰胆碱(ACh)释放的增加。使用一种新型荧光标记技术来选择性地可视化大鼠脑片中活的隔海马胆碱能神经元,我们发现毒蕈碱激动剂并不会兴奋隔海马胆碱能神经元,相反,它们会抑制一部分胆碱能神经元。相比之下,通过逆行标记和双标记技术证实为非胆碱能的未标记神经元,即隔海马GABA型神经元,会被毒蕈碱强烈兴奋。因此,毒蕈碱类药物在MSDB中增强认知的作用不能归因于海马体中ACh释放的增加。相反,由隔海马GABA能通路中冲动流增加引起的去抑制机制可能是毒蕈碱激动剂增强认知作用的基础。
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