Publicover S J
Brain Res. 1985 Apr 29;333(1):185-7. doi: 10.1016/0006-8993(85)90144-1.
Treatment of frog neuromuscular preparations with the protein kinase C activator 12-O-tetradecanoylphorbol-13-acetate (TPA) (100 nM) resulted in a 40% rise in the frequency of miniature endplate potentials (MEPPs) (P less than 0.05). When these experiments were repeated on preparations bathed in saline containing 10 mM K+ (a procedure that raises MEPP frequency by approximately 10-fold due to the elevated level of [Ca2+]i), TPA caused a 70-75% increase in MEPP frequency (P less than 0.02), although the data did not differ significantly from those recorded in standard frog saline due to the variability between preparations. It is concluded that transmitter release mechanisms may be modulated by protein kinase C and that such modulation probably acts synergistically with [Ca2+]i.
用蛋白激酶C激活剂12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)(100 nM)处理青蛙神经肌肉标本,导致微小终板电位(MEPPs)频率升高40%(P < 0.05)。当在含有10 mM K⁺的盐溶液中浸泡的标本上重复这些实验时(由于细胞内Ca²⁺水平升高,该操作使MEPP频率提高约10倍),TPA使MEPP频率增加70 - 75%(P < 0.02),尽管由于标本间的变异性,数据与在标准青蛙盐溶液中记录的数据无显著差异。结论是,递质释放机制可能受蛋白激酶C调节,且这种调节可能与细胞内Ca²⁺协同作用。