Bartfai T, Vizi E S
Arch Int Pharmacodyn Ther. 1986 Dec;284(2):212-24.
The calcium channel blocker, nimodipine (Bay e 9736), inhibited the evoked (1 Hz, 1 msec, 180 pulses) release of [14C]acetylcholine ([14C]ACh) while it enhanced the release of [3H]noradrenaline ([3H]NA) measured concomitantly from the same longitudinal muscle strip of guinea-pig ileum loaded with [14C]choline and [3H]noradrenaline. These effects of nimodipine were concentration-dependent: in 0.1 microM concentration yielding maximal inhibition of [14C]ACh release and in 0.5 microM concentration yielding half maximal stimulation of [3H]NA-release. Enhancement of [3H]NA-release by nimodipine was strongly dependent on stimulation frequency while the inhibitory effect of nimodipine on release of [14C]ACh did not depend on stimulation frequency in the 0.5-10 Hz range. In addition, in the presence of nimodipine when the release of [3H]NA was enhanced, i.e. when a significant negative feedback operation could have been expected, alpha 2-adrenoceptor blocking agents (yohimbine and idazoxane) failed to enhance [3H]NA-release. It is proposed that nimodipine somehow exerts a presynaptic alpha 2-adrenoceptor blocking property at noradrenergic axon terminals through an effect on calcium entry, which may be an essential step in events linking alpha 2-adrenoceptor activation and inhibition of noradrenaline release.
钙通道阻滞剂尼莫地平(Bay e 9736)抑制了诱发的(1赫兹,1毫秒,180个脉冲)[14C]乙酰胆碱([14C]ACh)释放,同时增强了从装载有[14C]胆碱和[3H]去甲肾上腺素的豚鼠回肠同一段纵行肌条中同时测得的[3H]去甲肾上腺素([3H]NA)释放。尼莫地平的这些作用具有浓度依赖性:在0.1微摩尔浓度时对[14C]ACh释放产生最大抑制,在0.5微摩尔浓度时对[3H]NA释放产生半数最大刺激。尼莫地平对[3H]NA释放的增强强烈依赖于刺激频率,而尼莫地平对[14C]ACh释放的抑制作用在0.5 - 10赫兹范围内不依赖于刺激频率。此外,在存在尼莫地平时,当[3H]NA释放增强时,即当可能预期有显著的负反馈作用时,α2 - 肾上腺素能受体阻断剂(育亨宾和伊达唑新)未能增强[3H]NA释放。有人提出,尼莫地平通过对钙内流的影响,以某种方式在去甲肾上腺素能轴突终末发挥突触前α2 - 肾上腺素能受体阻断特性,这可能是连接α2 - 肾上腺素能受体激活与去甲肾上腺素释放抑制的事件中的一个关键步骤。