Bosch F, Morales M, Badia A, Baños J E
Departament de Farmacologia i Psiquiatria, Facultat Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain.
Eur J Pharmacol. 1992 Nov 3;222(1):163-6. doi: 10.1016/0014-2999(92)90832-o.
The effects of velnacrine (1-hydroxytacrine), tacrine and physostigmine on indirectly elicited twitch at low and high stimulation frequencies were analyzed in the rat phrenic hemidiaphragm preparation. At 0.2 Hz, velnacrine and physostigmine behaved in a similar manner, the latter showing a higher potentiating effect. This potentiation was observed at 3-100 microM velnacrine, whereas a slight depression appeared at higher concentrations. When tetanic responses were studied, the drug concentrations needed to depress tetanic tension and tetanic fade were quite different in the case of velnacrine (depression of tetanic tension from 1 microM and tetanic fade from 170 microM), whereas physostigmine and tacrine were able to affect these parameters at very similar concentrations. The results suggest that some effects of velnacrine could differ from those of tacrine in spite of the chemical similarity.
在大鼠膈半横膈肌标本中,分析了维那克林(1-羟基他克林)、他克林和毒扁豆碱在低刺激频率和高刺激频率下对间接诱发抽搐的影响。在0.2Hz时,维那克林和毒扁豆碱表现相似,后者的增强作用更强。在3-100μM维那克林浓度下观察到这种增强作用,而在更高浓度时则出现轻微抑制。当研究强直反应时,维那克林降低强直张力和强直衰减所需的药物浓度差异很大(从1μM开始降低强直张力,从170μM开始出现强直衰减),而毒扁豆碱和他克林能够在非常相似的浓度下影响这些参数。结果表明,尽管维那克林与他克林化学结构相似,但某些作用可能不同。