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母体暴露于白细胞介素-1β后,丝裂原活化蛋白激酶途径的激活诱导豚鼠胎儿肺液吸收。

Stimulation of MAP kinase pathways after maternal IL-1beta exposure induces fetal lung fluid absorption in guinea pigs.

作者信息

Bhattacharjee Reshma, Li Tianbo, Koshy Shyny, Beard LaMonta L, Sharma Kapil, Carter Ethan P, Garat Chrystelle, Folkesson Hans G

机构信息

Department of Physiology and Pharmacology, Northeastern Ohio Universities College of Medicine, Rootstown, OH 44272-0095, USA.

出版信息

Respir Res. 2007 Mar 26;8(1):27. doi: 10.1186/1465-9921-8-27.

Abstract

BACKGROUND

We tested the hypothesis that maternal interleukin-1beta (IL-1beta) pretreatment and induction of fetal cortisol synthesis activates MAP kinases and thereby affects lung fluid absorption in preterm guinea pigs.

METHODS

IL-1beta was administered subcutaneously daily to timed-pregnant guinea pigs for three days. Fetuses were obtained by abdominal hysterotomy and instilled with isosmolar 5% albumin into the lungs and lung fluid movement was measured over 1 h by mass balance. MAP kinase expression was measured by western blot.

RESULTS

Lung fluid absorption was induced at 61 days (D) gestation and stimulated at 68D gestation by IL-1beta. Maternal IL-1beta pretreatment upregulated ERK and upstream MEK expression at both 61 and 68D gestation, albeit being much more pronounced at 61D gestation. U0126 instillation completely blocked IL-1beta-induced lung fluid absorption as well as IL-1beta-induced/stimulated ERK expression. Cortisol synthesis inhibition by metyrapone attenuated ERK expression and lung fluid absorption in IL-1beta-pretreated fetal lungs. JNK expression after maternal IL-1beta pretreatment remained unaffected at either gestation age.

CONCLUSION

These data implicate the ERK MAP kinase pathway as being important for IL-1beta induction/stimulation of lung fluid absorption in fetal guinea pigs.

摘要

背景

我们检验了这样一个假设,即母体白细胞介素-1β(IL-1β)预处理和诱导胎儿皮质醇合成会激活丝裂原活化蛋白激酶(MAP激酶),从而影响早产豚鼠的肺液吸收。

方法

对定时怀孕的豚鼠每天皮下注射IL-1β,持续三天。通过腹部子宫切开术获取胎儿,并向其肺内注入等渗5%白蛋白,通过质量平衡法在1小时内测量肺液移动情况。通过蛋白质免疫印迹法测量MAP激酶表达。

结果

在妊娠61天(D)时诱导了肺液吸收,在妊娠68D时IL-1β刺激了肺液吸收。母体IL-1β预处理在妊娠61天和68D时均上调了细胞外信号调节激酶(ERK)和上游丝裂原活化蛋白激酶/细胞外信号调节激酶激酶(MEK)的表达,尽管在妊娠61D时更为明显。注入U0126完全阻断了IL-1β诱导的肺液吸收以及IL-1β诱导/刺激的ERK表达。甲吡酮抑制皮质醇合成减弱了IL-1β预处理的胎儿肺中的ERK表达和肺液吸收。母体IL-1β预处理后,妊娠各年龄的应激活化蛋白激酶(JNK)表达均未受影响。

结论

这些数据表明ERK MAP激酶途径对于IL-1β诱导/刺激豚鼠胎儿肺液吸收很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f008/1847817/2b762f43aaed/1465-9921-8-27-1.jpg

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