Dar D E, Zinder O
Department of Clinical Biochemistry, Rambam Medical Center, Haifa, Israel.
Naunyn Schmiedebergs Arch Pharmacol. 1995 Jul;352(1):11-6. doi: 10.1007/BF00169184.
The effect of strychnine on evoked release of catecholamines from a primary culture of bovine adrenal medullary cells was investigated. Strychnine at > 1 microM inhibited catecholamine release stimulated by 10 microM acetylcholine, or 10 microM nicotine, but not by excess K+ (59 mM), the sodium ionophore veratridine (100 microM) or the calcium ionophore A-23187 (10 microM). The inhibitory response elicited by exposure of the cells to strychnine was rapid (< 3 min) and competitive with acetylcholine. High concentrations of acetylcholine (1 mM) completely overcame this inhibition. Strychnine might be acting on a regulatory site of the nicotinic-cholinergic receptor, which is genetically similar to the strychnine-binding 48 KD subunit of the glycine receptor.
研究了士的宁对牛肾上腺髓质细胞原代培养物中儿茶酚胺诱发释放的影响。浓度大于1微摩尔的士的宁可抑制由10微摩尔乙酰胆碱或10微摩尔尼古丁刺激引起的儿茶酚胺释放,但对过量钾离子(59毫摩尔)、钠离子载体藜芦碱(100微摩尔)或钙离子载体A - 23187(10微摩尔)刺激引起的儿茶酚胺释放无抑制作用。细胞暴露于士的宁引起的抑制反应迅速(<3分钟),且与乙酰胆碱存在竞争性。高浓度的乙酰胆碱(1毫摩尔)可完全克服这种抑制作用。士的宁可能作用于烟碱型胆碱能受体的一个调节位点,该位点在基因上与甘氨酸受体的48千道尔顿士的宁结合亚基相似。