Elliott R C
Gen Pharmacol. 1987;18(1):7-11. doi: 10.1016/0306-3623(87)90160-1.
Lidocaine (0.92 mM) potentiated tetraethylammonium (TEA, 0.6-6 mM) induced contractures of the chick biventer cervicis muscle (BVC) in vitro. The dose ratio for TEA (EC50 in lidocaine/EC50 control) was 1.16 X 10(-3). Lidocaine (0.92 mM) blocked nerve and muscle action potentials in the BVC preparation, blocked slow fibre MEPPS, and blocked indirectly elicited muscle contraction. Lidocaine (0.92 mM) non-competitively blocked acetylcholine (ACh) induced contractures of the chick BVC. Gallamine competitively blocked ACh contractures (pA2 6.53) but produced only a relatively weak non-competitive block of TEA induced contractures in lidocaine. TEA induced contractures of the chick BVC in the presence of lidocaine probably do not involve ACh.
利多卡因(0.92毫摩尔)增强了四乙铵(TEA,0.6 - 6毫摩尔)在体外诱导的鸡双颈二腹肌(BVC)挛缩。TEA的剂量比(利多卡因中的半数有效浓度/对照中的半数有效浓度)为1.16×10⁻³。利多卡因(0.92毫摩尔)阻断了BVC标本中的神经和肌肉动作电位,阻断了慢纤维微小终板电位,并阻断了间接引发的肌肉收缩。利多卡因(0.92毫摩尔)非竞争性地阻断了乙酰胆碱(ACh)诱导的鸡BVC挛缩。加拉明竞争性地阻断了ACh挛缩(亲和力常数pA2为6.53),但对利多卡因存在时TEA诱导的挛缩仅产生相对较弱的非竞争性阻断作用。利多卡因存在时TEA诱导的鸡BVC挛缩可能不涉及ACh。