Sumida T, Smith M A, Maehara Y, Collins J G, Kitahata L M
Department of Anesthesiology, Yale University School of Medicine, New Haven, CT 06510, USA.
Pain. 1998 Feb;74(2-3):307-13. doi: 10.1016/s0304-3959(97)00191-7.
The effects of spinally administered R(-)N6-(2-phenylisopropyl) adenosine (R-PIA) on spinal dorsal horn neurons were investigated in anesthetized rats. Extracellular, single-unit recordings were measured during noxious heating of receptive fields on the hind paw. Three series of experiments were carried out to characterize the effects of R-PIA on spinal dorsal horn neuronal activity. In the first set of experiments, R-PIA dose-dependently suppressed noxiously evoked activity of spinal dorsal horn neurons. In the second set of experiments, R-PIA suppressed noxiously evoked activity in neurons sensitized by the topical application of mustard oil to a region of skin adjacent to their receptive fields. In the third set of experiments, R-PIA prevented mustard oil induced sensitization of dorsal horn neurons. In all cases, the adenosine receptor antagonist theophylline reversed the action of R-PIA. The results of these investigations indicate the involvement of spinal adenosine receptors in spinal pathways of central sensitization and in the modulation of somatically induced noxious pain.
在麻醉大鼠中研究了脊髓给予R(-)N6-(2-苯异丙基)腺苷(R-PIA)对脊髓背角神经元的影响。在后爪感受野进行有害热刺激时,测量细胞外单单位记录。进行了三组实验以表征R-PIA对脊髓背角神经元活动的影响。在第一组实验中,R-PIA剂量依赖性地抑制脊髓背角神经元的有害刺激诱发活动。在第二组实验中,R-PIA抑制了因在其感受野相邻皮肤区域局部应用芥子油而致敏的神经元的有害刺激诱发活动。在第三组实验中,R-PIA预防了芥子油诱导的背角神经元致敏。在所有情况下,腺苷受体拮抗剂茶碱可逆转R-PIA的作用。这些研究结果表明脊髓腺苷受体参与了中枢敏化的脊髓通路以及对躯体诱导的有害疼痛的调节。