Jiang C, Cummins T R, Haddad G G
Department of Pediatrics (Section of Respiratory Medicine) Yale University School of Medicine, New Haven, CT 06520-8064.
Exp Brain Res. 1994;100(3):407-20. doi: 10.1007/BF02738401.
It is well known that neuronal firing properties are determined by synaptic inputs and inherent membrane functions such as specific ionic currents. To characterize the ionic currents of brainstem cardio-respiratory neurons, cells from the hypoglossal (XII) nucleus and the dorsal motor nucleus of the vagus (DMX) were freshly dissociated and membrane ionic currents were studied under whole-cell voltage and current clamp. Both of these neurons showed a TTX-sensitive Na+ current with a much larger current density in XII than DMX neurons. This Na+ current had two (fast and slow) distinct inactivation decay components. The ratio of the magnitudes of the fast to slow component was roughly two-fold greater in DMX than in XII cells. Both DMX and XII neurons also showed a high voltage-activated Ca2+ current, but this current density was significantly greater (three-fold) in DMX than XII neurons. A relatively small amount of low-voltage activated Ca2+ current was also observed in DMX neurons, but not in the majority of XII cells. A transient and a sustained outward current components were observed in DMX cells, but only sustained currents were present in XII neurons. These outward currents had a reversal potential of about -70 mV with 3 mM external K+ and -30 mV with 25 mM K+, and substitution of K+ with cesium and tetraethylammonium suppressed more than 90% the outward currents, indicating that most outward currents were carried by K+. The transient outward current consisted of two components with one sensitive to 4-aminopyridine and the other to intracellular Ca2+. In XII neurons, BRL 38227 (lemakalim), an ATP-sensitive K+ (KATP) channel activator, increased the sustained K+ currents by 10% of control, and glibenclamide, a KATP channel blocker, decreased the sustained K+ currents by 20%. Evidence for the presence of an inward rectifier K+ current was also obtained from both XII and DMX neurons. These results on XII and DMX neurons indicate that (1) the methods used to dissociate neurons provide a useful means to overcome voltage clamp technical difficulties; (2) ion channel characteristics such as density and biophysical properties of DMX neurons are very different from those of XII neurons; and (3) several newly discovered membrane ionic currents are present in these cells.
众所周知,神经元的放电特性由突触输入和诸如特定离子电流等固有的膜功能所决定。为了表征脑干心肺神经元的离子电流,将来自舌下神经(XII)核和迷走神经背运动核(DMX)的细胞新鲜解离,并在全细胞电压钳和电流钳下研究膜离子电流。这两种神经元均表现出对河豚毒素(TTX)敏感的Na⁺电流,XII神经元中的电流密度比DMX神经元大得多。这种Na⁺电流具有两个(快速和慢速)不同的失活衰减成分。DMX中快速成分与慢速成分的幅度比大约是XII细胞中的两倍。DMX和XII神经元均还表现出高电压激活的Ca²⁺电流,但该电流密度在DMX中比XII神经元显著更大(三倍)。在DMX神经元中还观察到相对少量的低电压激活的Ca²⁺电流,但在大多数XII细胞中未观察到。在DMX细胞中观察到一个瞬态外向电流成分和一个持续外向电流成分,但在XII神经元中仅存在持续电流。这些外向电流在外部K⁺浓度为3 mM时的反转电位约为 -70 mV,在外部K⁺浓度为25 mM时为 -30 mV,用铯和四乙铵替代K⁺可抑制超过90%的外向电流,表明大多数外向电流由K⁺携带。瞬态外向电流由两个成分组成,一个对4-氨基吡啶敏感,另一个对细胞内Ca²⁺敏感。在XII神经元中,ATP敏感性钾(KATP)通道激活剂BRL 38227(雷马卡林)使持续K⁺电流增加了对照的10%,而KATP通道阻滞剂格列本脲使持续K⁺电流减少了20%。在XII和DMX神经元中均获得了内向整流钾电流存在的证据。这些关于XII和DMX神经元的结果表明:(1)用于解离神经元的方法为克服电压钳技术难题提供了一种有用的手段;(2)DMX神经元的离子通道特性,如密度和生物物理特性,与XII神经元非常不同;(3)这些细胞中存在几种新发现的膜离子电流。