Morisset V, Urban L
Novartis, London WC1E 6BN, United Kingdom.
J Neurophysiol. 2001 Jul;86(1):40-8. doi: 10.1152/jn.2001.86.1.40.
The effect of cannabinoids on excitatory transmission in the substantia gelatinosa was investigated using intracellular recording from visually identified neurons in a transverse slice preparation of the juvenile rat spinal cord. In the presence of strychnine and bicuculline, perfusion of the cannabinoid receptor agonist WIN55,212-2 reduced the frequency and the amplitude of spontaneous excitatory postsynaptic currents (sEPSCs). Furthermore, the frequency of miniature EPSCs (mEPSCs) was also decreased by WIN55,212-2, whereas their amplitude was not affected. Similar effects were reproduced using the endogenous cannabinoid ligand anandamide. The effects of both agonists were blocked by the selective CB(1) receptor antagonist SR141716A. Electrical stimulation of high-threshold fibers in the dorsal root evoked a monosynaptic EPSC in lamina II neurons. In the presence of WIN55,212-2, the amplitude of the evoked EPSC (eEPSCs) was reduced, and the paired-pulse ratio was increased. The reduction of the eEPSC following CB(1) receptor activation was unlikely to have a postsynaptic origin because the response to AMPA, in the presence of 1 microM TTX, was unchanged. To investigate the specificity of this synaptic inhibition, we selectively activated the nociceptive C fibers with capsaicin, which induced a strong increase in the frequency of EPSCs. In the presence of WIN55,212-2, the response to capsaicin was diminished. In conclusion, these results strongly suggest a presynaptic location for CB(1) receptors whose activation results in inhibition of glutamate release in the spinal dorsal horn. The strong inhibitory effect of cannabinoids on C fibers may thereby contribute to the modulation of the spinal excitatory transmission, thus producing analgesia at the spinal level.
利用幼年大鼠脊髓横切片制备中视觉识别神经元的细胞内记录,研究了大麻素对脊髓背角胶状质兴奋性传递的影响。在存在士的宁和荷包牡丹碱的情况下,灌注大麻素受体激动剂WIN55,212-2可降低自发兴奋性突触后电流(sEPSCs)的频率和幅度。此外,WIN55,212-2也降低了微小兴奋性突触后电流(mEPSCs)的频率,而其幅度未受影响。使用内源性大麻素配体花生四烯乙醇胺也得到了类似的结果。两种激动剂的作用均被选择性CB(1)受体拮抗剂SR141716A阻断。电刺激背根中的高阈值纤维可在II层神经元中诱发单突触兴奋性突触后电流(eEPSC)。在存在WIN55,212-2的情况下,诱发的EPSC(eEPSCs)幅度降低,成对脉冲比率增加。CB(1)受体激活后eEPSC的降低不太可能源于突触后,因为在存在1 microM 河豚毒素(TTX)的情况下,对α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)的反应未改变。为了研究这种突触抑制的特异性,我们用辣椒素选择性激活伤害性C纤维,辣椒素可诱导EPSCs频率大幅增加。在存在WIN55,212-2的情况下,对辣椒素的反应减弱。总之,这些结果强烈表明CB(1)受体位于突触前,其激活导致脊髓背角谷氨酸释放受到抑制。大麻素对C纤维的强烈抑制作用可能有助于调节脊髓兴奋性传递,从而在脊髓水平产生镇痛作用。