Reyes-Vázquez C, Dafny N
Appl Neurophysiol. 1983;46(5-6):254-60. doi: 10.1159/000101271.
Sprague-Dawley rats anesthetized with urethane were used to study the single cell responses of medial thalamic neurons following noxious input and their interactions with gamma-aminobutyric acid (GABA) agonist THIP (4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3-ol) and morphine sulfate applied microintophoretically . The majority of the medial thalamic neurons responded to noxious stimulation by an increase in their firing rate. Local application of both THIP and morphine attenuated the spontaneous and the noxious evoked responses of these neurons. The possibility of a role for GABA in mediating nonopiate pain suppression is discussed.
用氨基甲酸乙酯麻醉的Sprague-Dawley大鼠,研究丘脑内侧神经元在伤害性输入后的单细胞反应,以及它们与通过微量电泳施加的γ-氨基丁酸(GABA)激动剂THIP(4,5,6,7-四氢异恶唑并[5,4-c]吡啶-3-醇)和硫酸吗啡的相互作用。大多数丘脑内侧神经元通过增加放电频率对伤害性刺激做出反应。局部应用THIP和吗啡均减弱了这些神经元的自发反应和伤害性诱发反应。本文讨论了GABA在介导非阿片类疼痛抑制中发挥作用的可能性。