Criado-Fornelio A, de Armas-Serra C, Jimenez-Gonzalez A, Casado-Escribano N, Rodriguez-Caabeiro F
Parasitology and Microbiology Department, Faculty of Pharmacy, University of Alcalá de Henares, Madrid, Spain.
Parasitol Res. 1990;76(6):518-20. doi: 10.1007/BF00931057.
Biochemical changes produced by luxabendazole in muscle-stage Trichinella spiralis larvae consisted of a decrease in free glucose and glycogen levels (46.71% and 35.66%, respectively) after in vivo treatment, slight in vitro inhibition of fumarate reductase activity (24.15%) and, finally, inhibition of [3H]-colchicine-tubulin binding, which was found to be of a competitive nature, with an inhibition constant (Ki) of 0.9 x 10(-7) M. In a parallel study, luxabendazole did not appear to be inhibitory to [3H]-colchicine binding to pig-brain tubulin.
体内处理后游离葡萄糖和糖原水平降低(分别降低46.71%和35.66%),体外对延胡索酸还原酶活性有轻微抑制(24.15%),最后抑制[3H]-秋水仙碱与微管蛋白的结合,发现这种抑制具有竞争性,抑制常数(Ki)为0.9×10⁻⁷M。在一项平行研究中,鲁苯达唑似乎对[3H]-秋水仙碱与猪脑微管蛋白的结合没有抑制作用。