Onimaru Hiroshi, Ballanyi Klaus, Homma Ikuo
Department of Physiology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142, Japan.
J Physiol. 2003 Nov 1;552(Pt 3):727-41. doi: 10.1113/jphysiol.2003.049312. Epub 2003 Aug 22.
Ca2+-dependent conductances were studied in respiratory interneurons in the brainstem-spinal cord preparation of newborn rats. omega-Conotoxin-GVIA attenuated evoked postsynaptic potentials, spontaneous or evoked inspiratory spinal nerve activity and blocked spike afterhyperpolarization. Furthermore, omega-conotoxin-GVIA augmented rhythmic drive potentials of pre-inspiratory and inspiratory neurons and increased respiratory-related spike frequency of pre-inspiratory cells with no effect on inspiratory hyperpolarization. In contrast, omega-agatoxin-IVA depressed drive potentials of pre-inspiratory and inspiratory neurons and attenuated inspiratory hyperpolarization and spike frequency of pre-inspiratory cells. It did not affect spike shape and exerted only minor, non-significant, attenuating effects on spontaneous or evoked nerve bursts or evoked postsynaptic potentials. Nifedipine diminished drive potentials and spike frequency of pre-inspiratory neurons and shortened drive potentials in some cells. omega-Conotoxin-MVIIC attenuated drive potentials and intraburst firing rate of pre-inspiratory neurons and decreased substantially respiratory frequency. Respiratory rhythm disappeared following combined application of omega-conotoxin-GVIA, omega-conotoxin-MVIIC, omega-agatoxin-IVA and nifedipine. Apamin potentiated drive potentials and abolished spike afterhyperpolarization, whereas charybdotoxin and tetraethylammonium prolonged spike duration without effect on shape of drive potentials. The results show that specific sets of voltage-activated L-, N- and P/Q-type Ca2+ channels determine the activity of particular subclasses of neonatal respiratory neurons, whereas SK- and BK-type K+ channels attenuate drive potentials and shorten spikes, respectively, independent of cell type. We hypothesize that modulation of spontaneous activity of pre-inspiratory neurons via N-, L- and P/Q-type Ca2+ channels is important for respiratory rhythm or pattern generation.
在新生大鼠脑干-脊髓标本中的呼吸中间神经元中研究了钙依赖性电导。ω-芋螺毒素-GVIA减弱了诱发的突触后电位、自发或诱发的吸气性脊髓神经活动,并阻断了动作电位后的超极化。此外,ω-芋螺毒素-GVIA增强了吸气前和吸气神经元的节律性驱动电位,并增加了吸气前细胞与呼吸相关的动作电位频率,而对吸气超极化无影响。相比之下,ω-阿加毒素-IVA降低了吸气前和吸气神经元的驱动电位,减弱了吸气超极化和吸气前细胞的动作电位频率。它不影响动作电位的形状,对自发或诱发的神经爆发或诱发的突触后电位仅产生轻微的、无统计学意义的减弱作用。硝苯地平降低了吸气前神经元的驱动电位和动作电位频率,并缩短了一些细胞的驱动电位。ω-芋螺毒素-MVIIC减弱了吸气前神经元的驱动电位和爆发内放电率,并显著降低了呼吸频率。联合应用ω-芋螺毒素-GVIA、ω-芋螺毒素-MVIIC、ω-阿加毒素-IVA和硝苯地平后呼吸节律消失。蜂毒明肽增强了驱动电位并消除了动作电位后的超极化,而大蝎毒素和四乙铵延长了动作电位持续时间,但对驱动电位的形状无影响。结果表明,特定的电压激活L型、N型和P/Q型钙通道决定了新生呼吸神经元特定亚类的活动,而SK型和BK型钾通道分别减弱驱动电位和缩短动作电位,与细胞类型无关。我们假设通过N型、L型和P/Q型钙通道对吸气前神经元自发活动的调节对于呼吸节律或模式的产生很重要。