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两种新型免疫抑制剂FK506和苔藓抑素B对小鼠妊娠的影响。

The effect of two new immunosuppressive agents, FK506 and didemnin B, in murine pregnancy.

作者信息

Farley D E, Shelby J, Alexander D, Scott J R

机构信息

Department of Obstetrics and Gynecology, University of Utah Medical Center, Salt Lake City 84132.

出版信息

Transplantation. 1991 Jul;52(1):106-10. doi: 10.1097/00007890-199107000-00022.

Abstract

The purpose of this study was to investigate two promising immunosuppressive agents, didemnin B (DB) and FK506 (FK), during pregnancy to assess potential adverse maternal or fetal effects. Pregnant C3H mice were randomized into control and high- and low-dose treatment groups for each drug. Animals received daily injections from day 1 to day 16, and on day 17 of gestation the maternal condition, litter size, fetal resorption rates, and fetal/placental unit weights were determined. Immunoglobulin (IgG) levels were obtained for DB treatment groups. Delayed type hypersensitivity was assessed in virgin females. Both DB and FK had dose-dependent immunosuppressive activity in the DTH assay, and DB caused elevated IgG concentrations. High doses of DB caused diarrhea and maternal wasting with no fetal survival; with low-dose DB, maternal weight gain was depressed, but pregnancy outcome was not different from control animals. High-dose FK had no obvious detrimental effects on maternal health but caused resorption of all fetuses; administration of low-dose FK resulted in a higher number of resorptions, but fetuses that survived did not appear different from controls. We conclude that these immunosuppressive drugs can have adverse effects on pregnancy, but the maternal and fetal toxicity are dose-dependent.

摘要

本研究的目的是在孕期研究两种有前景的免疫抑制剂,苔藓抑素B(DB)和他克莫司(FK506,FK),以评估对母体或胎儿可能产生的不良影响。将怀孕的C3H小鼠随机分为对照组以及每种药物的高剂量和低剂量治疗组。动物从第1天到第16天每天接受注射,在妊娠第17天测定母体状况、产仔数、胎儿吸收发生率以及胎儿/胎盘单位重量。获取DB治疗组的免疫球蛋白(IgG)水平。对未孕雌性小鼠进行迟发型超敏反应评估。在迟发型超敏反应试验中,DB和FK均具有剂量依赖性免疫抑制活性,且DB导致IgG浓度升高。高剂量的DB导致腹泻和母体消瘦,无胎儿存活;低剂量的DB使母体体重增加受到抑制,但妊娠结局与对照动物无异。高剂量的FK对母体健康无明显有害影响,但导致所有胎儿吸收;低剂量FK给药导致更多胎儿吸收,但存活的胎儿与对照无差异。我们得出结论,这些免疫抑制药物可对妊娠产生不良影响,但其母体和胎儿毒性具有剂量依赖性。

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