首页> 美国卫生研究院文献>The Journal of Physiology >Inhibition of α7-containing nicotinic ACh receptors by muscarinic M1 ACh receptors in rat hippocampal CA1 interneurones in slices
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Inhibition of α7-containing nicotinic ACh receptors by muscarinic M1 ACh receptors in rat hippocampal CA1 interneurones in slices

机译:毒蕈碱型M1 ACh受体对大鼠海马CA1中间神经元切片中烟碱型ACh受体的抑制作用

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摘要

Cys-loop ligand-gated nicotinic ACh receptors (nAChRs) and G protein-coupled muscarinic ACh receptors (mAChRs) are expressed on rat hippocampal interneurones where they can regulate excitability, synaptic communication and cognitive function. Even though both nAChRs and mAChRs appear to co-localize to the same interneurones, it is not clear whether there is crosstalk between them. We utilized patch-clamp techniques to investigate this issue in rat hippocampal CA1 interneurones in slices under conditions where synaptic transmission was blocked. The α7 nAChR-mediated currents were activated by choline, and when the activation of this receptor was preceded by the activation of the M1 mAChR subtype, the amplitude of α7 responses was significantly reduced in a rapidly reversible and voltage-independent manner, without any change in the kinetics of responses. This M1 mAChR-mediated inhibition of α7 nAChRs was through a PLC-, calcium- and PKC-dependent signal transduction cascade. These data show that M1 mAChRs and α7 nAChRs are functionally co-localized on individual rat hippocampal interneurones where the activation of these particular mAChRs inhibits α7 nAChR function. This information will help to understand how these cholinergic receptor systems might be regulating neuronal excitability in the hippocampus in a manner that has relevance for synaptic plasticity and cognition.
机译:半胱氨酸环配体门控烟碱型ACh受体(nAChRs)和G蛋白偶联毒蕈碱型ACh受体(mAChRs)在大鼠海马中间神经元上表达,它们可以调节兴奋性,突触通讯和认知功能。即使nAChR和mAChR似乎都共同定位于相同的中间神经元,但尚不清楚它们之间是否存在串扰。我们利用膜片钳技术来研究在突触传递受阻的条件下大鼠海马CA1中间神经元的切片中的这一问题。 α7nAChR介导的电流被胆碱激活,当该受体的激活先于M1 mAChR亚型的激活时,α7反应的幅度以快速可逆且与电压无关的方式显着降低,而没有任何改变在反应动力学中。 M1 mAChR介导的对α7nAChRs的抑制作用是通过依赖PLC,钙和PKC的信号转导级联来实现的。这些数据表明,M1 mAChR和α7nAChR在功能上共定位于单个大鼠海马中间神经元,其中这些特定mAChR的激活抑制α7nAChR的功能。这些信息将有助于了解这些胆碱能受体系统可能如何以与突触可塑性和认知相关的方式调节海马神经元兴奋性。

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