Kato M, Hashimoto Y, Horinouchi T, Ando T, Ito J, Yamanaka H
Department of Anesthesiology, Tohoku University Postgraduate Medical School, 1-1 Seiryo-machi, Aoba-ku, Sendai 980-8574, Japan.
J Anesth. 2000 Jan 20;14(1):30-4. doi: 10.1007/s005400050006.
The kinetics of the inhibition of human plasma cholinesterase (ChE) and erythrocyte acetylcholinesterase (AChE) by alcuronium, atracurium, d-tubocurarine, pancuronium, pipecuronium, and vecuronium were studied in blood drawn from 35 surgical patients.
The activities of plasma ChE and erythrocyte AChE were determined by the calorimetric method of Ellman et al., using acetylthiocholine as the substrate. Lineweaver-Burk plots and Dixon plots were used for the analysis of the kinetics of both enzymes.
The dissociation constants (K(m)) of plasma ChE and erythrocyte AChE were 5.00 x 10(-5) M and 5.28 x 10(-5) M, respectively, indicating that both enzymes have similar affinity to acetylthiocholine. Both Lineweaver-Burk plots and Dixon plots indicated that the six nondepolarizing neuromuscular blocking agents (NMBAs) at different concentrations induce linear mixed-type inhibition. The apparent inhibition constants (K(i)) of pancuronium (8.72 x 10(-8) M) and vecuronium (3.53 x 10(-7) M) for plasma ChE inhibition were lower than that of neostigmine (7.36 x 10(-7) M), whereas those of the six nondepolarizing NMBAs for erythrocyte AChE were markedly higher than that of neostigmine.
Both plasma ChE and erythrocyte AChE were inhibited by six nondepolarizing NMBAs, and the pattern of inhibition of both enzymes was of mixed type. The inhibitory potencies of pancuronium and vecuronium for plasma ChE were larger than that of neostigmine, whereas those of the six nondepolarizing NMBAs for erythrocyte AChE were markedly lower than that of neostigmine. The rank order of relative potency for plasma ChE was pancuronium > vecuronium > pipecuronium > alcuronium > d-tubocurarine > atracurium.
研究阿库氯铵、阿曲库铵、d-筒箭毒碱、泮库溴铵、哌库溴铵和维库溴铵对35例外科手术患者血液中人体血浆胆碱酯酶(ChE)和红细胞乙酰胆碱酯酶(AChE)的抑制动力学。
采用Ellman等人的比色法,以乙酰硫代胆碱为底物,测定血浆ChE和红细胞AChE的活性。用Lineweaver-Burk图和Dixon图分析两种酶的动力学。
血浆ChE和红细胞AChE的解离常数(K(m))分别为5.00×10(-5) M和5.28×10(-5) M,表明两种酶对乙酰硫代胆碱具有相似的亲和力。Lineweaver-Burk图和Dixon图均表明,不同浓度的六种非去极化神经肌肉阻滞剂(NMBA)均诱导线性混合型抑制。泮库溴铵(8.72×10(-8) M)和维库溴铵(3.53×10(-7) M)对血浆ChE抑制的表观抑制常数(K(i))低于新斯的明(7.36×10(-7) M),而六种非去极化NMBA对红细胞AChE的表观抑制常数明显高于新斯的明。
六种非去极化NMBA均抑制血浆ChE和红细胞AChE,且两种酶的抑制模式均为混合型。泮库溴铵和维库溴铵对血浆ChE的抑制效力大于新斯的明,而六种非去极化NMBA对红细胞AChE的抑制效力明显低于新斯的明。血浆ChE相对效力的排序为泮库溴铵>维库溴铵>哌库溴铵>阿库氯铵>d-筒箭毒碱>阿曲库铵。