Pica-Mattoccia L, Cioli D
J Parasitol. 1986 Aug;72(4):531-9.
Visual observation of the motor activity of Schistosoma mansoni kept in vitro showed an increase of activity in the presence of hycanthone (HC). In addition, HC caused a delay in the paralytic effects of carbachol. Similar results were observed in the presence of oxamniquine (OXA). The same pattern of motor activity, however, was shown by HC-resistant worms, by Schistosoma japonicum, and by worms exposed to drug precursors (lucanthone and UK-3883), which are not schistosomicidal in vitro. Other analogs with in vitro killing activity (IA-4 and IA-4 N-oxide) showed minimal anticholinergic effects. The anticholinergic effects of HC and OXA were quickly reversible in vitro and in vivo, whereas their antischistosomal effects are irreversible and delayed. Incubation of schistosomes with high concentrations of carbachol or with anticholinergic drugs failed to compete with the schistosomicidal effects of HC. These results are viewed as contradictory to the hypothesis that HC kills schistosomes by blocking their acetylcholine receptors.
对体外培养的曼氏血吸虫运动活性的视觉观察显示,在海恩酮(HC)存在的情况下活性增加。此外,HC导致卡巴胆碱麻痹作用延迟。在奥沙尼喹(OXA)存在的情况下也观察到类似结果。然而,对HC耐药的虫体、日本血吸虫以及暴露于体外无杀血吸虫活性的药物前体(卢坎酮和UK - 3883)的虫体表现出相同的运动活性模式。其他具有体外杀伤活性的类似物(IA - 4和IA - 4 N -氧化物)显示出最小的抗胆碱能作用。HC和OXA的抗胆碱能作用在体外和体内均可快速逆转,而它们的抗血吸虫作用是不可逆且延迟的。用高浓度卡巴胆碱或抗胆碱能药物孵育血吸虫未能与HC的杀血吸虫作用竞争。这些结果被认为与HC通过阻断其乙酰胆碱受体杀死血吸虫这一假设相矛盾。