Pore R S
Drug Chem Toxicol. 1984;7(1):57-71. doi: 10.3109/01480548409014173.
Chlorella protothecoides accelerated the detoxification of chlordecone poisoned rats, decreasing the half-life of the toxin from 40 to 19 days. The ingested algae passed through the gastrointestinal tract unharmed , interrupted the enteric recirculation of the persistent insecticide, and subsequently eliminated the bound chlordecone with the feces. The detoxification was similar to that obtained with cholestyramine. Laboratory preparations were made to determine whether cell-free components retained the therapeutic properties of the whole cells. Acid and alkaline hydrolysis of the algae destroyed the cells except for the resistant cell wall components. One component was sporopollenin , a carotenoid polymer of limited natural occurrence among microorganisms and plants. Plant sporopollenin was not active, but algal cell walls and sporopollenin retained the therapeutic activity of the whole cells. The cells and cell walls have potential as detoxifying drugs for animals poisoned by chlordecone and other xenobiotic compounds with similar properties.
原球藻加速了被十氯酮毒害大鼠的解毒过程,使毒素的半衰期从40天缩短至19天。摄入的藻类安然无恙地通过胃肠道,中断了持久性杀虫剂的肠肝循环,随后随粪便排出结合态的十氯酮。这种解毒作用与使用消胆胺所获得的效果相似。制备了实验室制剂以确定无细胞成分是否保留全细胞的治疗特性。藻类的酸解和碱解破坏了细胞,仅留下抗性细胞壁成分。其中一种成分是孢粉素,它是一种在微生物和植物中天然存在有限的类胡萝卜素聚合物。植物孢粉素没有活性,但藻类细胞壁和孢粉素保留了全细胞的治疗活性。这些细胞和细胞壁有潜力作为被十氯酮和其他具有类似性质的外源性化合物毒害的动物的解毒药物。