Horn A S, Lambert J J, Marshall I G
Br J Pharmacol. 1979 Jan;65(1):53-62. doi: 10.1111/j.1476-5381.1979.tb17333.x.
1 4-Aminopyridine methiodide (4-APMI), a quaternary analogue of aminopyridine (4-AP), was tested for neuromuscular facilitatory actions on the chick biventer cervicis and frog sartorius nerve-muscle preparations. 2 In the chick, 4-APMI (10(-4) to 10(-2) M) augmented indirectly elicited twitches and reversed tubocurarine-induced neuromuscular block. Reversal of tubocurarine block was observed after treatment of the muscle with an anticholinesterase. 4-APMI did not itself produce contracture but augmented responses to added acetylcholine. 3 4-APMI (10(-4) M) prolonged the time courses of endplate potentials (e.p.ps) and miniature endplate potentials (m.e.p.ps) in the frog. 4 4-APMI (10(-4) M) increased e.p.p. quantal content. 4-AP was about 100 times more active than 4-APMI in increasing quantal content. Both compounds prolonged muscle action potentials at similar concentrations. 5 4-APMI (10(-3) to 3 X 10(-3) M) possessed anticholinesterase activity in homogenates of chick biventer cervicis muscle. 6 It is concluded that 4-APMI increases evoked acetylcholine release and also possesses a weak anticholinesterase action. The greater action of 4-AP on quantal content is probably due to an intracellular action, possibly involving the release of calcium ions.
4-氨基吡啶甲碘化物(4-APMI)是氨基吡啶(4-AP)的季铵类似物,对鸡颈二腹肌和蛙缝匠肌神经-肌肉标本进行了神经肌肉促进作用测试。
在鸡身上,4-APMI(10⁻⁴至10⁻²M)增强间接诱发的抽搐,并逆转筒箭毒碱诱导的神经肌肉阻滞。在用抗胆碱酯酶处理肌肉后,观察到筒箭毒碱阻滞的逆转。4-APMI本身不产生挛缩,但增强对添加乙酰胆碱的反应。
4-APMI(10⁻⁴M)延长了蛙终板电位(e.p.ps)和微小终板电位(m.e.p.ps)的时间进程。
4-APMI(10⁻⁴M)增加了e.p.p.的量子含量。在增加量子含量方面,4-AP的活性比4-APMI高约100倍。两种化合物在相似浓度下都延长了肌肉动作电位。
4-APMI(10⁻³至3×10⁻³M)在鸡颈二腹肌肌肉匀浆中具有抗胆碱酯酶活性。
得出结论,4-APMI增加诱发的乙酰胆碱释放,并且还具有微弱的抗胆碱酯酶作用。4-AP对量子含量的更大作用可能是由于细胞内作用,可能涉及钙离子的释放。