du Pont J S
Department of Experimental Zoology, University of Amsterdam, The Netherlands.
Acta Endocrinol (Copenh). 1990 Jul;123(1):51-60. doi: 10.1530/acta.0.1230051.
Electrophysiological experiments show that T3 has a direct effect on the cell membrane of GH3 cells, a transformed line from the rat pituitary. Slope conductance versus membrane potential, resting membrane resistance, potential, capacity and action potentials were measured in this study. Using a current clamp technique, the effects of tetrodotoxin, tetraethylammonium, apamin, and nifedipine were measured and compared with those directly evoked by T3. T3 increased the slope conductance: 1. at around -60 mV, as did tetrodotoxin (Na+ channel blocker); 2. at about -40 mV, as did nifedipine (Ca2+ channel blocker), but decreased this conductance strongly between -20 and -30 mV, as did both nifedipine and apamin (Ca2(+)-sensitive K+ channel blocker). Action potentials were inhibited by T3 and by nifedipine. Action potentials in these cells are primarily related to Ca2+ ions. It seems that T3 inhibits the Ca2+ current and, as a consequence, the Ca2(+)-sensitive K+ current.
电生理实验表明,T3对GH3细胞(一种源自大鼠垂体的转化细胞系)的细胞膜有直接作用。本研究测量了斜率电导与膜电位、静息膜电阻、电位、电容和动作电位。采用电流钳技术,测量了河豚毒素、四乙铵、蜂毒明肽和硝苯地平的作用,并与T3直接诱发的作用进行了比较。T3增加了斜率电导:1. 在约-60 mV时,与河豚毒素(钠通道阻滞剂)的作用相同;2. 在约-40 mV时,与硝苯地平(钙通道阻滞剂)的作用相同,但在-20至-30 mV之间强烈降低了这种电导,与硝苯地平和蜂毒明肽(钙敏感钾通道阻滞剂)的作用相同。动作电位受到T3和硝苯地平的抑制。这些细胞中的动作电位主要与钙离子有关。似乎T3抑制了钙电流,因此也抑制了钙敏感钾电流。