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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Presynaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors modulate release of inhibitory amino acids in rat spinal cord dorsal horn.
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Presynaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors modulate release of inhibitory amino acids in rat spinal cord dorsal horn.

机译:突触前α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体调节大鼠脊髓背角中抑制性氨基酸的释放。

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摘要

Local inhibition within the spinal cord dorsal horn is mediated by the neurotransmitters GABA and glycine and strongly influences nociceptive and temperature signaling. Alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors are expressed by inhibitory interneurons and have been shown to modulate GABA release in other regions of the CNS. In the spinal cord, there is morphological evidence for presynaptic AMPA receptor subunits in GABAergic dorsal horn neurons, but functional data are lacking. To determine if AMPA receptors are indeed functional at presynaptic terminals of inhibitory neurons, we recorded evoked and miniature inhibitory postsynaptic currents (mIPSPs) in the superficial dorsal horn of the rat spinal cord. We show that AMPA receptor activation enhances spontaneous release of inhibitory amino acids in the presence of tetrodotoxin onto both lamina II neurons and NK1 receptor-expressing (NK1R+) lamina I neurons. This effect is sensitive to the concentration of extracellular Ca2+, yet is not fully blocked in most neurons in the presence of Cd2+, suggesting possible Ca2+ entry through AMPA receptors. Postsynaptic Ca2+ elevation is not required for these changes. AMPA-induced increases in mIPSP frequency are also seen in more mature dorsal horn neurons, indicating that these receptors may play a role in nociceptive processing in the adult. In addition, we have observed AMPA-induced depression of evoked release of GABA and glycine onto lamina I NK1R+ neurons. Taken together these data support a role for presynaptic AMPA receptors in modulating release of GABA and glycine in the superficial dorsal horn. Because inhibition in the dorsal horn is important for controlling pain signaling, presynaptic AMPA receptors acting to modulate the inhibitory inputs onto dorsal horn neurons would be expected to impact upon pain signaling in the spinal cord dorsal horn.
机译:脊髓背角内的局部抑制作用由神经递质GABA和甘氨酸介导,并强烈影响伤害感受和温度信号。 α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体由抑制性中间神经元表达,并已被证明可调节CNS其他区域的GABA释放。在脊髓中,存在GABA能级背角神经元中突触前AMPA受体亚基的形态学证据,但缺乏功能数据。为了确定AMPA受体在抑制神经元的突触前末端是否确实起作用,我们在大鼠脊髓的浅背角记录了诱发的和微型的抑制突触后电流(mIPSPs)。我们显示AMPA受体激活增强河豚毒素对层II神经元和NK1受体表达(NK1R +)层I神经元的河豚毒素的存在时自发释放抑制性氨基酸。这种作用对细胞外Ca2 +的浓度敏感,但是在存在Cd2 +的大多数神经元中并未被完全阻断,表明Ca2 +可能通过AMPA受体进入。这些变化不需要突触后Ca2 +升高。 AMPA诱导的mIPSP频率增加也出现在更成熟的背角神经元中,表明这些受体可能在成人的伤害感受过程中起作用。此外,我们已经观察到AMPA诱导的GABA和甘氨酸诱发释放到层状NK1R +神经元上的抑制。总之,这些数据支持突触前AMPA受体在调节浅表背角中GABA和甘氨酸释放中的作用。因为在背角的抑制对于控制疼痛信号传导很重要,所以预期突触前AMPA受体的作用是将抑制性输入调节到背角神经元上,从而影响脊髓背角的疼痛信号传导。

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