Schofield G G, Furman B L, Marshall I G
Acta Diabetol Lat. 1978 Sep-Dec;15(5-6):287-93. doi: 10.1007/BF02590752.
Preparations from alloxan diabetic rats showed a reduced sensitivity to the neuromuscular blocking action of (+)-tubocurarine but no alteration in sensitivity to the depolarizing neuromuscular blocking drug decamethonium. Physostigmine was less effective in augmenting twitch height in preparations from alloxan diabetic rats and such preparations had a significantly lowered total cholinesterase activity compared with control preparations. An additional observation was a reduction in the effectiveness of the pre-junctionally active agent beta-bungarotoxin in producing neuromuscular blockade in physostigmine-treated preparations from alloxan diabetic rats. All the changes produced by alloxan administration were prevented by treatment with insulin.
来自四氧嘧啶糖尿病大鼠的制剂对(+)-筒箭毒碱的神经肌肉阻断作用敏感性降低,但对去极化神经肌肉阻断药十烃季铵的敏感性无改变。毒扁豆碱增强四氧嘧啶糖尿病大鼠制剂中肌肉收缩高度的效果较差,且与对照制剂相比,此类制剂的总胆碱酯酶活性显著降低。另一观察结果是,在毒扁豆碱处理的四氧嘧啶糖尿病大鼠制剂中,接头前活性药物β-银环蛇毒素产生神经肌肉阻滞的有效性降低。给予胰岛素可预防四氧嘧啶给药所产生的所有变化。