Komai Hirochika, McDowell Thomas S
Department of Anesthesiology, School of Medicine and Public Health, University of Wisconsin-Madison, WI 53762-3272, United States.
Neurosci Lett. 2007 May 18;418(3):298-303. doi: 10.1016/j.neulet.2007.03.041. Epub 2007 Mar 23.
Neuraxial analgesia is often provided using a mixture of local anesthetics and opioids. This combination of agents provides better pain relief and is generally associated with fewer side effects than when either drug is given alone. Local anesthetics have been shown to alter signaling of other G protein-coupled receptors, but little is known about their effect on opioid receptor signaling. Because opioids produce analgesia at least in part by inhibiting presynaptic Ca channels, we have evaluated the effects of tetracaine and bupivacaine on opioid-mediated inhibition of Ca channels in dorsal root ganglion neurons. The mu-opioid specific agonist DAMGO (1microM) inhibited Ca channels in both the absence and presence of tetracaine (50 or 100muM). However, the extent of DAMGO inhibition in the presence of both concentrations of tetracaine was less than that observed in the absence of tetracaine. DAMGO inhibition decreased from 39.2+/-24.4% in control to 34.2+/-24.4% with 50microM tetracaine (n=16; p<0.05), and from 40.5+/-19.6% in control to 34.6+/-20.5% with 100microM tetracaine (n=10; p<0.05). Similar results were seen with bupivacaine. Tetracaine also decreased the voltage-dependent facilitation of Ca channel currents when G proteins were activated by either DAMGO or the non-hydrolyzable GTP analogue (GTPgammaS), suggesting that tetracaine weakens the interaction between G protein betagamma subunits and the Ca channel. Overall, these results suggest that local anesthetics decrease opioid inhibition of Ca channel activity by interfering with the GTP-mediated signal transduction between opioid receptors and Ca channels.
神经轴索镇痛通常使用局部麻醉药和阿片类药物的混合物。与单独使用任何一种药物相比,这种药物组合能提供更好的疼痛缓解,且通常副作用更少。已表明局部麻醉药会改变其他G蛋白偶联受体的信号传导,但对其对阿片受体信号传导的影响知之甚少。由于阿片类药物至少部分通过抑制突触前钙通道产生镇痛作用,我们评估了丁卡因和布比卡因对背根神经节神经元中阿片类药物介导的钙通道抑制作用的影响。μ-阿片特异性激动剂DAMGO(1μM)在不存在和存在丁卡因(50或100μM)的情况下均抑制钙通道。然而,在两种浓度丁卡因存在下DAMGO的抑制程度均低于不存在丁卡因时观察到的程度。DAMGO的抑制作用从对照中的39.2±24.4%降至50μM丁卡因时的34.2±24.4%(n =16;p<),从对照中的40.5±19.6%降至100μM丁卡因时的34.6±20.5%(n =10;p<)。布比卡因也得到了类似的结果。当G蛋白被DAMGO或不可水解的GTP类似物(GTPγS)激活时,丁卡因还降低了钙通道电流的电压依赖性易化作用,这表明丁卡因削弱了G蛋白βγ亚基与钙通道之间的相互作用。总体而言,这些结果表明局部麻醉药通过干扰阿片受体与钙通道之间的GTP介导的信号转导来降低阿片类药物对钙通道活性的抑制作用。