Okanlawon A O, Ejiwunmi A B, Dada M O, Ashiru O A
Department of Anatomy, College of Medicine, University of Lagos, Nigeria.
West Afr J Med. 1991 Apr-Jun;10(2):171-4.
The Antimalaria drug, chloroquine is an amphiphilic cationic compound and might therefore be suspected to interfere with foetal lung maturity as previously observed with other amphilphilic cationic drugs. Single doses of chloroquine phosphate (40mg/kg b. wt) was administered to pregnant rats on days 20 and 21 of gestation (term = 22 days). Morphometric analysis revealed a decrease in volume density (Vv) of parenchyma, saccular space and average saccular volume. Concurrent administration of single doses hydrocortisone on day 21 increased the Vv of the Parenchyma saccules and average saccular volume. This result suggests that the retardation of foetal lung maturity induced by chloroquine could be reversed by a concurrent administration of hydrocortisone. Questions concerning the mechanism by which these effects are produced must remain open.
抗疟药物氯喹是一种两亲性阳离子化合物,因此可能会像之前观察到的其他两亲性阳离子药物那样,干扰胎儿肺成熟。在妊娠第20天和第21天(足月为22天)给怀孕大鼠单次注射磷酸氯喹(40mg/kg体重)。形态计量学分析显示,实质、囊状间隙和平均囊状体积的体积密度(Vv)降低。在第21天同时单次注射氢化可的松可增加实质囊泡的Vv和平均囊状体积。这一结果表明,氯喹诱导的胎儿肺成熟延迟可通过同时给予氢化可的松来逆转。关于产生这些效应的机制问题仍未解决。