Kilpatrick D L, Slepetis R, Kirshner N
J Neurochem. 1981 Jul;37(1):125-31. doi: 10.1111/j.1471-4159.1981.tb05299.x.
The effects of several neurotoxins and cholinergic antagonists on the nicotine-induced secretion of catecholamines by adrenal medulla cells in culture were investigated. Aconitine, veratridine, and batrachotoxin, in the presence of 1 micrometer-tetrodotoxin inhibited the nicotine-stimulated secretion of catecholamines in a dose-dependent manner in Locke's solution. In Na+-free sucrose medium, tetrodotoxin was not required to inhibit the stimulatory effects of aconitine, veratridine, and batrachotoxin, and these agents by themselves inhibited the nicotine-stimulated secretion of catecholamines. Scorpion venom, which also increases the flux of Na+ through tetrodotoxin-sensitive channels, was not an effective inhibitor of nicotine-stimulated secretion. Histrionicotoxin, atropine, hexamethonium, and decamethonium--as well as the Na+-channel activators--noncompetitively inhibit nicotine-stimulated secretion. The effects of these agents on nicotine-stimulated secretion appears similar to their effects on the inhibition of depolarization at the neuromuscular junction. Reversibility studies suggest that the stimulatory and inhibitor sites of the neurotoxins are different, while studies in Na+-free media suggest that tetrodotoxin-insensitive sodium channels are not involved in the inhibitory effect of the neurotoxins. A possible site of action for the inhibitory effects of the neurotoxins. A possible site of action for the inhibitory effects of the neurotoxins is the nicotinic-receptor-associated ion channel.
研究了几种神经毒素和胆碱能拮抗剂对培养的肾上腺髓质细胞尼古丁诱导的儿茶酚胺分泌的影响。在含有1微摩尔河豚毒素的情况下,乌头碱、藜芦碱和箭毒蛙毒素在洛克溶液中以剂量依赖的方式抑制尼古丁刺激的儿茶酚胺分泌。在无钠蔗糖培养基中,不需要河豚毒素来抑制乌头碱、藜芦碱和箭毒蛙毒素的刺激作用,这些药物自身就能抑制尼古丁刺激的儿茶酚胺分泌。蝎毒也能增加通过河豚毒素敏感通道的钠离子通量,但它不是尼古丁刺激分泌的有效抑制剂。组氨毒素、阿托品、六甲铵和十甲铵以及钠离子通道激活剂非竞争性地抑制尼古丁刺激的分泌。这些药物对尼古丁刺激分泌的作用似乎与其对神经肌肉接头处去极化抑制的作用相似。可逆性研究表明,神经毒素的刺激和抑制位点不同,而在无钠培养基中的研究表明,河豚毒素不敏感的钠通道不参与神经毒素的抑制作用。神经毒素抑制作用的一个可能作用位点。神经毒素抑制作用的一个可能作用位点是烟碱受体相关离子通道。