Corcoran J J, Kirshner N
J Neurochem. 1983 Apr;40(4):1106-9. doi: 10.1111/j.1471-4159.1983.tb08099.x.
The calcium-entry antagonist D600 (methoxyverapamil) inhibited nicotine- and veratridine-induced 45Ca2+ uptake, 22Na+ uptake, and catecholamine secretion in primary cultures of bovine adrenal medulla cells. Inhibition of nicotine-induced effects occurred at D600 concentrations approximately 3-10-fold lower than those needed to produce similar inhibition of veratridine-induced effects. Inhibition of the veratridine-induced effects was competitive, but inhibition of the nicotine-induced effects was not competitive. These results suggest that D600, in addition to blocking "slow" Ca2+ channels and tetrodotoxin-sensitive Na+ channels also blocks nicotine transmission, possibly either by noncompetitively inhibiting the interaction of nicotine with the receptor binding site or by blockade of the receptor-associated ion conductance channel.
钙内流拮抗剂D600(甲氧基维拉帕米)可抑制牛肾上腺髓质细胞原代培养物中尼古丁和藜芦碱诱导的45Ca2+摄取、22Na+摄取以及儿茶酚胺分泌。D600抑制尼古丁诱导作用的浓度比产生类似藜芦碱诱导作用抑制所需浓度低约3至10倍。对藜芦碱诱导作用的抑制具有竞争性,但对尼古丁诱导作用的抑制不具有竞争性。这些结果表明,D600除了阻断“慢”Ca2+通道和河豚毒素敏感的Na+通道外,还可能通过非竞争性抑制尼古丁与受体结合位点的相互作用或阻断受体相关离子传导通道来阻断尼古丁传递。