N-acetyl-cysteine suppresses amniotic fluid and placenta inflammatory cytokine responses to lipopolysaccharide in rats

被引:73
作者
Beloosesky, R
Gayle, DA
Amidi, F
Nunez, SE
Babu, J
Desai, M
Ross, MG
机构
[1] Harbor UCLA Med Ctr, Dept Obstet & Gynecol, Torrance, CA USA
[2] Harbor UCLA Med Ctr, Los Angeles Biomed Res Inst, Torrance, CA USA
关键词
N-acetyl-cysteine; maternal infection; inflammation; fetus; rat;
D O I
10.1016/j.ajog.2005.06.082
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Maternal infections may induce placental, amniotic and, potentially, fetal inflammatory responses. As cytokine responses may be mediated by oxidative stress, we determined whether the antioxidant N-acetyl-cysteine (NAC), can attenuate maternally induced amniotic and placental cytokine responses to maternal infection (modeled by lipopolysaccharide [LPS]). Study design: Gestation day 18 pregnant rats were (1) treated with LPS (100 mu g/kg, body weight; intraperitoneally) alone; (2) pretreated with NAC (300 mg/kg body weight; intraperitoneally) 30 minutes before LPS; (3) posttreated with NAC 120 minutes after LPS; or (4) treated with NAC 30 minutes before and 120 minutes after LPS. Six hours after LPS administration, maternal serum and amniotic fluid interleukin-6 (IL-6) and IL-10 levels, and placental IL-6 messenger RNA levels were determined. Results: LPS increased maternal serum IL-6 (50 +/- 25 to 3444 +/- 584 pg/mL) and IL-10 (40 +/- 20 to 958 +/- 339 pg/mL) and amniotic fluid IL-6 (59 +/- 25 to 891 +/- 128 pg/mL). Pretreatment and/ or posttreatnient with NAC attenuated IL-6 in the maternal serum and amniotic fluid and IL-10 in the amniotic fluid. LPS also induced placental IL-6 messenger RNA that was inhibited by treatment with NAC before and after LPS. Conclusion: NAC inhibition of inflammatory responses may protect the fetus from potential long-term sequelae. (c) 2006 Mosby, Inc. All rights reserved.
引用
收藏
页码:268 / 273
页数:6
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