Kimura I, Okazaki M, Nojima H
Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Sugitani, Japan.
Eur J Pharmacol. 1997 Jul 9;330(2-3):123-8. doi: 10.1016/s0014-2999(97)01003-0.
To investigate the mutual dependence of calcitonin gene-related peptide (CGRP) and acetylcholine release, we examined the effect of a cholinesterase inhibitor neostigmine on the release of CGRP-like immunoreactivity in rat phrenic nerve-hemidiaphragm muscle preparation, and conversely, the effect of CGRP on [3H]acetylcholine release from motor nerve terminals loaded with [3H]choline in the same preparations of mice. Release of CGRP-like immunoreactivity was increased by electrical nerve stimulation (train of 40 pulses of 200 micros pulse duration and frequency of 50 Hz applied every 10 s) in the whole preparation but not in the segmental preparation containing the endplate region. Neostigmine (0.1-0.3 microM) enhanced the resting release of CGRP-like immunoreactivity in a concentration-dependent manner, whereas it depressed the nerve-evoked release of CGRP-like immunoreactivity. CGRP (1 microM) added to perfusate decreased nerve-evoked [3H]acetylcholine release. These results suggest that CGRP, which is released by electrical nerve stimulation or a cholinesterase inhibitor in intact skeletal muscles, negatively modulates nerve-evoked acetylcholine release.
为研究降钙素基因相关肽(CGRP)与乙酰胆碱释放之间的相互依赖性,我们检测了胆碱酯酶抑制剂新斯的明对大鼠膈神经 - 半膈肌标本中CGRP样免疫反应性释放的影响,反之,检测了CGRP对相同小鼠标本中负载[³H]胆碱的运动神经末梢释放[³H]乙酰胆碱的影响。在整个标本中,通过电神经刺激(每10秒施加一次持续时间为200微秒、频率为50赫兹的40个脉冲串)可增加CGRP样免疫反应性的释放,但在含有终板区的节段性标本中则不然。新斯的明(0.1 - 0.3微摩尔)以浓度依赖性方式增强CGRP样免疫反应性的静息释放,而抑制神经诱发的CGRP样免疫反应性释放。灌注液中添加CGRP(1微摩尔)可减少神经诱发的[³H]乙酰胆碱释放。这些结果表明,在完整骨骼肌中由电神经刺激或胆碱酯酶抑制剂释放的CGRP对神经诱发的乙酰胆碱释放具有负性调节作用。