Sanfaçon R, Possmayer F, Harding P G
Am J Obstet Gynecol. 1977 Apr 1;127(7):745-52. doi: 10.1016/0002-9378(77)90250-2.
Pregnant guinea pigs of 50 to 53 days' gestation (term 63 days) were anesthetized with ether, and their fetuses were injected intramuscularly with 30 mg of dexamethasone or sterile saline. One week later, the fetuses were injected with 3H-thymidine intramuscularly under direct vision at laparotomy; after one hour, the incorporation of thymidine into deoxyribonucleic acid (DNA was analyzed in various fetal tissues. The relative labeling of DNA was significantly depressed in the cerebral hemispheres, cerebellum, medulla oblongata, and midbrain of the treated fetuses compared to their littermate controls. The relative labeling of the DNA of lungs, kidneys, heart, and adrenals was also significantly reduced. Increasing the dose of dexamethasone produced a progressive inhibition of the incorporation of 3H-thymidine into DNA. A variable recovery from the inhibition became apparent by 14 days following exposure to dexamethasone. The evidence suggests that exposure of the fetus to dexamethasone may exert a potentially deleterious effect on fetal tissues.
对妊娠50至53天(孕期63天)的豚鼠用乙醚进行麻醉,然后给其胎儿肌肉注射30毫克地塞米松或无菌生理盐水。一周后,在剖腹直视下给胎儿肌肉注射3H-胸腺嘧啶核苷;一小时后,分析各种胎儿组织中胸腺嘧啶核苷掺入脱氧核糖核酸(DNA)的情况。与同窝对照胎儿相比,经处理胎儿的大脑半球、小脑、延髓和中脑的DNA相对标记率显著降低。肺、肾、心脏和肾上腺的DNA相对标记率也显著降低。增加地塞米松剂量会逐渐抑制3H-胸腺嘧啶核苷掺入DNA。在接触地塞米松14天后,抑制作用出现了不同程度的恢复。有证据表明,胎儿接触地塞米松可能会对胎儿组织产生潜在的有害影响。