Engelman H S, Anderson R L, Daniele C, Macdermott A B
Department of Physiology and Cellular Biophysics and the Center for Neurobiology and Behavior, Columbia University, 630 West 168th Street, New York, NY 10032, USA.
Neuroscience. 2006 May 12;139(2):539-53. doi: 10.1016/j.neuroscience.2005.12.038. Epub 2006 Feb 10.
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.
脊髓背角内的局部抑制由神经递质γ-氨基丁酸(GABA)和甘氨酸介导,并强烈影响伤害性和温度信号传导。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,并已被证明可调节中枢神经系统其他区域的GABA释放。在脊髓中,有形态学证据表明GABA能背角神经元存在突触前AMPA受体亚基,但缺乏功能数据。为了确定AMPA受体在抑制性神经元的突触前终末是否确实具有功能,我们在大鼠脊髓背角浅层记录了诱发的和微小抑制性突触后电流(mIPSPs)。我们发现,在存在河豚毒素的情况下,AMPA受体激活可增强抑制性氨基酸向II层神经元和表达神经激肽-1受体(NK1R+)的I层神经元的自发释放。这种效应对细胞外Ca2+浓度敏感,但在大多数神经元中,在存在Cd2+的情况下并未完全被阻断,这表明可能有Ca2+通过AMPA受体进入。这些变化不需要突触后Ca2+升高。在更成熟的背角神经元中也观察到AMPA诱导的mIPSP频率增加,这表明这些受体可能在成人的伤害性处理中发挥作用。此外,我们还观察到AMPA诱导的GABA和甘氨酸向I层NK1R+神经元的诱发释放受到抑制。综上所述,这些数据支持突触前AMPA受体在调节背角浅层GABA和甘氨酸释放中发挥作用。由于背角内的抑制对于控制疼痛信号很重要,因此作用于调节背角神经元抑制性输入的突触前AMPA受体预计会影响脊髓背角的疼痛信号。