Loiseau P M, Trabelsi M, Madaule Y, Bories C, Wolf J G
Université de Paris-Sud, Chatenay-Malabry, France.
Arzneimittelforschung. 1996 Nov;46(11):1095-8.
Catecholamide spiroarsoranes were synthesized and evaluated for anthelmintic properties on two in vitro models, infective larvae of the filaria Molinema dessetae and infective larvae of an intestinal nematode. Nippostrongylus brasiliensis. On the N dessetae model, the most active compound after 24 h incubation time had an EC50 of 0.1 mumol/l. Eleven compounds had EC50 's in a range from 2 to 200 mumol/l. After 7 days incubation time, the two most active compounds had EC50 's of 0.03 and 0.07 mumol/l, respectively. On the N brasiliensis model, only three compounds were slightly active after 4 days incubation time. The ligands used for the spiroarsoranes synthesis were also evaluated for anthelmintic activity in order to know the contribution of these structures in the spiroarsoranes activity. Spiroarsoranes as prodrugs of arsonic acids were very active on the filaria, nematode having predominantly transcuticular uptake of nutrients while the activity on the intestinal nematode having both the types, transcuticular and intestinal uptake was low. The high sensitivity of filarial infective larvae is probably in relation to their location in the mosquito whereas N. brasiliensis infective larvae are telluric and should be more unsensitive to survive in a variable environment.
合成了儿茶酚胺螺砷烷,并在两种体外模型上评估了其驱虫特性,这两种模型分别是丝虫莫氏丝虫的感染性幼虫和肠道线虫巴西日圆线虫的感染性幼虫。在莫氏丝虫模型上,孵育24小时后最具活性的化合物的半数有效浓度(EC50)为0.1微摩尔/升。11种化合物的EC50在2至200微摩尔/升范围内。孵育7天后,两种最具活性的化合物的EC50分别为0.03和0.07微摩尔/升。在巴西日圆线虫模型上,孵育4天后只有三种化合物有轻微活性。还评估了用于合成螺砷烷的配体的驱虫活性,以便了解这些结构对螺砷烷活性的贡献。作为砷酸前药的螺砷烷对丝虫非常有效,丝虫主要通过经皮吸收营养物质,而对同时具有经皮和肠道吸收两种方式的肠道线虫的活性较低。丝虫感染性幼虫的高敏感性可能与其在蚊子体内的位置有关,而巴西日圆线虫感染性幼虫生活在陆地上,在多变的环境中生存时应该更不敏感。