Abstract

Using a model of birth asphyxia, we previously reported significant structural and functional deficits in the diaphragm muscle in spiny mice, deficits that are prevented by supplementing the maternal diet with 5% creatine from mid-pregnancy. The long-term effects of this exposure are unknown. Pregnant spiny mice were fed control or 5% creatine-supplemented diet for the second half of pregnancy, and fetuses were delivered by caesarean section with or without 7.5 min of in-utero asphyxia. Surviving pups were raised by a cross-foster dam until 33±2 days of age when they were euthanized to obtain the diaphragm muscle for ex-vivo study of twitch tension and muscle fatigue, and for structural and enzymatic analyses. Functional analysis of the diaphragm revealed no differences in single twitch contractile parameters between any groups. However, muscle fatigue, induced by stimulation of diaphragm strips with a train of pulses (330ms train/sec, 40Hz) for 300sec, was significantly greater for asphyxia pups compared with controls (p<0.05), and this did not occur in diaphragms of creatine + asphyxia pups. Birth asphyxia resulted in a significant increase in the proportion of glycolytic, fast-twitch fibres and a reduction in oxidative capacity of Type I and IIb fibres in male offspring, as well as reduced cross-sectional area of all muscle fibre types (Type I, IIa, IIb/d) in both males and females at 33 days of age. None of these changes were observed in creatine + asphyxia animals. Thus, the changes in diaphragm fatigue and structure induced by birth asphyxia persist long-term but are prevented by maternal creatine supplementation.

Highlights

  • Each year approximately 1–3 neonates in every 1000 suffer a period of oxygen (O2) deprivation at birth [1,2,3]

  • Survival rates in the immediate neonatal period (1 h) after our birth asphyxia protocol for this study are summarised in Table 1, and were similar to those observed in a previous study using this model [27]

  • The birth asphyxia protocol resulted in an overall survival rate of 59%, but this was lower for males (52%) than for females (69%)

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Summary

Introduction

Each year approximately 1–3 neonates in every 1000 suffer a period of oxygen (O2) deprivation at birth [1,2,3]. Birth asphyxia occurs all over the world, incidence and mortality rates are highest in remote areas, in low-income countries where healthcare is poor [4,5,6]. It can result from a variety of events including umbilical cord compression, protracted labour or placental abruption [1,3]. This is detrimental to tissues with high and fluctuating energy demands such as the brain and striated muscle, and in animal models of birth asphyxia this has been shown to result in the induction of apoptosis and subsequent tissue damage or loss [9,10,11,12]

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