Jahr C E, Jessell T M
J Neurosci. 1985 Aug;5(8):2281-9. doi: 10.1523/JNEUROSCI.05-08-02281.1985.
Intracellular recording techniques have been used to provide information on the identity of excitatory sensory transmitters released at synapses formed between dorsal root ganglion (DRG) and dorsal horn neurons maintained in cell culture. Explants of embryonic rat DRG were added to dissociated cultures of embryonic dorsal horn neurons and synaptic potentials were recorded intracellularly from dorsal horn neurons after DRG explant stimulation. More than 80% of dorsal horn neurons within 1 mm of DRG explants received at least one fast, DRG-evoked, monosynaptic input. In the presence of high divalent cation concentrations, the acidic amino acid receptor agonists, L-glutamate, kainate, and quisqualate excited all dorsal horn neurons which received a monosynaptic DRG neuron input, whereas aspartate and N-methyl-D-aspartate (NMDA) had little or no action. Several compounds reported to antagonize the actions of acidic amino acids were tested for their ability to block DRG-evoked synaptic potentials and glutamate-evoked responses in dorsal horn neurons. 2-Amino-5-phosphonovalerate, a selective NMDA receptor antagonist, was relatively ineffective at antagonizing DRG-evoked synaptic potentials and glutamate-evoked responses. In contrast, kynurenate was found to be a potent antagonist of amino acid-evoked responses and of synaptic transmission at all DRG-dorsal horn synapses examined. The blockade of synaptic transmission by kynurenate appeared to result from a postsynaptic action on dorsal horn neurons. These findings indicate that glutamate, or a glutamate-like compound, but not aspartate, is the excitatory transmitter that mediates fast excitatory postsynaptic potentials at the DRG-dorsal horn synapses examined in this study.
细胞内记录技术已被用于提供有关在细胞培养中维持的背根神经节(DRG)和背角神经元之间形成的突触处释放的兴奋性感觉递质身份的信息。将胚胎大鼠DRG的外植体添加到胚胎背角神经元的解离培养物中,并在刺激DRG外植体后从背角神经元细胞内记录突触电位。在距离DRG外植体1毫米范围内的背角神经元中,超过80%至少接受了一个快速的、由DRG诱发的单突触输入。在高浓度二价阳离子存在的情况下,酸性氨基酸受体激动剂L-谷氨酸、海人酸和quisqualate兴奋了所有接受单突触DRG神经元输入的背角神经元,而天冬氨酸和N-甲基-D-天冬氨酸(NMDA)几乎没有作用。测试了几种据报道可拮抗酸性氨基酸作用的化合物阻断DRG诱发的突触电位和背角神经元中谷氨酸诱发反应的能力。2-氨基-5-磷酸戊酸,一种选择性NMDA受体拮抗剂,在拮抗DRG诱发的突触电位和谷氨酸诱发反应方面相对无效。相比之下,犬尿酸被发现是在所检查的所有DRG-背角突触处氨基酸诱发反应和突触传递的有效拮抗剂。犬尿酸对突触传递的阻断似乎是由于对背角神经元的突触后作用。这些发现表明,谷氨酸或类似谷氨酸的化合物,而不是天冬氨酸,是在本研究中所检查的DRG-背角突触处介导快速兴奋性突触后电位的兴奋性递质。