Abstract

BackgroundWe tested the hypothesis that maternal interleukin-1β (IL-1β) pretreatment and induction of fetal cortisol synthesis activates MAP kinases and thereby affects lung fluid absorption in preterm guinea pigs.MethodsIL-1β 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.ResultsLung fluid absorption was induced at 61 days (D) gestation and stimulated at 68D gestation by IL-1β. Maternal IL-1β 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-1β-induced lung fluid absorption as well as IL-1β-induced/stimulated ERK expression. Cortisol synthesis inhibition by metyrapone attenuated ERK expression and lung fluid absorption in IL-1β-pretreated fetal lungs. JNK expression after maternal IL-1β pretreatment remained unaffected at either gestation age.ConclusionThese data implicate the ERK MAP kinase pathway as being important for IL-1β induction/stimulation of lung fluid absorption in fetal guinea pigs.

Highlights

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

  • Rising endogenous epinephrine levels near term contribute to a decreased alveolar fluid volume, increased Na absorption, and induction of lung fluid absorption [3,4,5,6]

  • Maternal IL-1β exposure in guinea pigs induced fetal lung fluid absorption by activating the hypothalamus-pituitary-adrenal gland axis [3,16]. This led to fetal cortisol synthesis, which in turn increased membrane expression of β-adrenoceptors, Na,K-ATPases, and epithelial Na channels (ENaC) as well as induced fetal lung fluid absorption

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Summary

Introduction

We tested the hypothesis that maternal interleukin-1β (IL-1β) pretreatment and induction of fetal cortisol synthesis activates MAP kinases and thereby affects lung fluid absorption in preterm guinea pigs. Cytokines, such as IL-1, have been proposed to signal parturition onset [11]. Maternal IL-1β exposure in guinea pigs induced fetal lung fluid absorption by activating the hypothalamus-pituitary-adrenal gland axis [3,16]. This led to fetal cortisol synthesis, which in turn increased membrane expression of β-adrenoceptors (βAR), Na,K-ATPases, and ENaC as well as induced fetal lung fluid absorption

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