Nakajima T, Hazama H, Hamada E, Omata M, Kurachi Y
Second Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.
Pflugers Arch. 1995 Aug;430(4):552-62. doi: 10.1007/BF00373892.
Neurokinin A (NKA) caused single tracheal smooth muscle cells (TSMCs) to contract. The effects of NKA on the electrical activity of guinea-pig TSMCs were examined using the tight-seal whole-cell patch-clamp technique. Under current-clamp conditions at rest, the membrane potential of TSMCs spontaneously oscillated at about -40 mV and NKA rapidly depolarized the membrane potential to nearly 0 mV, which then gradually repolarized to about -20 mV in the presence of NKA. The oscillations in potential disappeared transiently during the rapid phase of depolarization in response to NKA and reappeared during the sustained phase of depolarization. Under voltage-clamp conditions, NKA evoked an inward current which faded quickly. Subsequently, the cell conductance in the presence of NKA at potentials greater than -40 mV decreased gradually. The reversal potential of the NKA-induced inward current was about 0 mV, and shifted with changes in the Cl- equilibrium potential. The Cl- current was not elicited by NKA when using a pipette solution containing 10 mM ethylenebis(oxonitrilo)tetraacetic acid (EGTA). During the sustained phase, K+ currents evoked by depolarizing voltage steps were inhibited by NKA. The present results indicate that NKA causes rapid and sustained depolarization of TSMCs by two distinct mechanisms: (1) initial transient activation of the Ca(2+)-dependent Cl- current, and (2) sustained inhibition of K+ currents.
神经激肽A(NKA)可引起单个气管平滑肌细胞(TSMCs)收缩。采用紧密密封全细胞膜片钳技术研究了NKA对豚鼠TSMCs电活动的影响。在静息状态下的电流钳条件下,TSMCs的膜电位自发振荡于约-40 mV,NKA可迅速使膜电位去极化至接近0 mV,随后在NKA存在的情况下逐渐复极化至约-20 mV。在对NKA去极化的快速阶段,电位振荡短暂消失,并在去极化的持续阶段重新出现。在电压钳条件下,NKA诱发一个迅速衰减的内向电流。随后,在电位大于-40 mV时,NKA存在下的细胞电导逐渐降低。NKA诱导的内向电流的反转电位约为0 mV,并随Cl-平衡电位的变化而移动。当使用含有10 mM乙二胺四乙酸(EGTA)的移液管溶液时,NKA不会引发Cl-电流。在持续阶段,去极化电压阶跃诱发的K+电流受到NKA的抑制。目前的结果表明,NKA通过两种不同机制导致TSMCs快速且持续的去极化:(1)Ca(2+)依赖性Cl-电流的初始短暂激活,以及(2)K+电流的持续抑制。