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成年GluR1基因敲除小鼠和野生型小鼠CA1神经元中,一氧化氮依赖的长时程增强需要突触后动作电位。

Postsynaptic action potentials are required for nitric-oxide-dependent long-term potentiation in CA1 neurons of adult GluR1 knock-out and wild-type mice.

作者信息

Phillips Keith G, Hardingham Neil R, Fox Kevin

机构信息

Cardiff School of Biosciences, Cardiff University, Cardiff CF10 3AX, UK.

出版信息

J Neurosci. 2008 Dec 24;28(52):14031-41. doi: 10.1523/JNEUROSCI.3984-08.2008.

Abstract

Neocortical long-term potentiation (LTP) consists of both presynaptic and postsynaptic components that rely on nitric oxide (NO) and the GluR1 subunit of the AMPA receptor, respectively. In this study, we found that hippocampal LTP, induced by theta-burst stimulation in mature (>8-week-old) GluR1 knock-out mice was almost entirely NO dependent and involved both the alpha splice variant of NO synthase-1 and the NO synthase-3 isoforms of NO synthase. Theta-burst induced LTP was also partly NO-dependent in wild-type mice and made up approximately 50% of the potentiation 2 h after tetanus. Theta-burst stimulation reliably produced postsynaptic spikes, including a high probability of complex spikes. Inhibition of postsynaptic somatic spikes with intracellular QX314 or local TTX application prevented LTP in the GluR1 knock-out mice and also blocked the NO component of LTP in wild types. We conclude that theta-burst stimulation is particularly well suited to producing the postsynaptic somatic spikes required for NO-dependent LTP.

摘要

新皮质长期增强(LTP)由突触前和突触后成分组成,分别依赖于一氧化氮(NO)和AMPA受体的GluR1亚基。在本研究中,我们发现,在成熟(>8周龄)的GluR1基因敲除小鼠中,由theta波爆发刺激诱导的海马LTP几乎完全依赖于NO,并涉及一氧化氮合酶-1的α剪接变体和一氧化氮合酶的一氧化氮合酶-3亚型。theta波爆发诱导的LTP在野生型小鼠中也部分依赖于NO,并且在强直刺激后2小时占增强作用的约50%。theta波爆发刺激可靠地产生突触后尖峰,包括高概率的复合尖峰。用细胞内QX314或局部应用TTX抑制突触后体细胞尖峰可阻止GluR1基因敲除小鼠中的LTP,并也阻断野生型中LTP的NO成分。我们得出结论,theta波爆发刺激特别适合于产生NO依赖性LTP所需的突触后体细胞尖峰。

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