Budai D, Harasawa I, Fields H L
Departments of Neurology and Physiology and the W. M. Keck Center for Integrative Neuroscience, University of California, San Francisco, California 94143-0114, USA.
J Neurophysiol. 1998 Nov;80(5):2244-54. doi: 10.1152/jn.1998.80.5.2244.
Modulation of sacral spinal dorsal horn neurons by the ventrolateral PAG was studied by extracellular recording combined with microiontophoretic applications of alpha-adrenergic agonists or antagonists. Bicuculline (BIC, 15 ng) microinjected into the ventrolateral PAG produced a consistent inhibition of the responses of nociceptive dorsal horn neurons. After PAG-BIC applications, the total number of spikes per heat stimulation period was significantly decreased to a mean of 37 +/- 19% (n = 8) of the pre-BIC control. Local iontophoresis of the selective alpha2-adrenoceptor antagonists idazoxan or yohimbine but not the selective alpha1 antagonist benoxathian significantly reversed PAG-BIC-evoked inhibition. At low ejection currents, clonidine, an alpha2-adrenoceptor agonist, markedly reduced noxious heat-evoked responses but had no consistent action on the responses to iontophoresed excitatory amino acids [EAA; N-methyl--aspartate (NMDA) or kainic acid]. At ejection currents higher than required to block descending inhibition, idazoxan potentiated responses to both heat and EAA iontophoresis. At higher ejection currents, EAA responses were inhibited by clonidine. This indicates that both presynaptic and postsynaptic alpha2 receptors are capable of inhibiting the recorded neurons. Activation of the alpha1 adrenoceptors by iontophoresis of methoxamine often led to a marked increase in the responses to kainic acid and, to a lesser extent, to NMDA iontophoresis or noxious heat. Together with previously reported work, the current experiments demonstrate that PAG neurons inhibit nociceptive dorsal horn neurons primarily through an indirect alpha2 adrenoceptor mechanism. In this same population of dorsal horn neurons, norepinephrine has a direct alpha1-mediated excitatory effect.
通过细胞外记录结合α-肾上腺素能激动剂或拮抗剂的微量离子导入应用,研究了腹外侧导水管周围灰质(ventrolateral PAG)对骶髓背角神经元的调制作用。向腹外侧导水管周围灰质微量注射荷包牡丹碱(BIC,15纳克)可对伤害性背角神经元的反应产生持续抑制。在应用PAG-BIC后,每个热刺激期的总尖峰数显著减少至BIC应用前对照值的平均37±19%(n = 8)。选择性α2-肾上腺素能拮抗剂咪唑克生或育亨宾的局部离子导入可显著逆转PAG-BIC诱发的抑制,而选择性α1拮抗剂贝诺沙嗪则无此作用。在低喷射电流下,α2-肾上腺素能激动剂可乐定可显著降低伤害性热诱发的反应,但对离子导入兴奋性氨基酸[EAA;N-甲基-D-天冬氨酸(NMDA)或 kainic 酸]的反应无一致作用。在高于阻断下行抑制所需的喷射电流时,咪唑克生增强了对热和EAA离子导入的反应。在较高喷射电流下,可乐定抑制EAA反应。这表明突触前和突触后α2受体均能够抑制所记录的神经元。通过甲氧明的离子导入激活α1肾上腺素能受体通常会导致对 kainic 酸的反应显著增加,对NMDA离子导入或伤害性热的反应增加程度较小。与先前报道的工作一起,当前实验表明PAG神经元主要通过间接的α2肾上腺素能受体机制抑制伤害性背角神经元。在同一群背角神经元中,去甲肾上腺素具有直接的α1介导的兴奋作用。