Ohnishi S T, Sadanaga K K, Katsuoka M, Weidanz W P
Membrane Research Institute, Philadelphia, PA 19104.
Mol Cell Biochem. 1989;91(1-2):159-65. doi: 10.1007/BF00228091.
The effects of several membrane-acting drugs on malaria and sickle cell anemia was studied. In the initial experiments, propranolol and W-7 were shown to increase red cell density. In vitro, these drugs inhibited the growth of P. falciparum. However, in vivo experiments using the murine malarial parasite, P. vinckei, demonstrated little, if any, anti-parasite activity with the doses of drugs employed. Subsequently, prostaglandin oligomeric derivatives were found to inhibit the growth of P. falciparum in vitro and P. vinckei in vivo. Since prostaglandin oligomers inhibited the formation of dense, dehydrated cells (irreversible sickle cells), they may also have therapeutic efficacy in sickle cell anemia.
研究了几种作用于细胞膜的药物对疟疾和镰状细胞贫血的影响。在最初的实验中,普萘洛尔和W-7可增加红细胞密度。在体外,这些药物可抑制恶性疟原虫的生长。然而,在使用鼠疟原虫文氏疟原虫进行的体内实验中,所用剂量的药物几乎没有(如果有也极少)抗寄生虫活性。随后,发现前列腺素低聚物衍生物在体外可抑制恶性疟原虫的生长,在体内可抑制文氏疟原虫的生长。由于前列腺素低聚物可抑制致密、脱水细胞(不可逆镰状细胞)的形成,它们在镰状细胞贫血中可能也具有治疗效果。