Dyson Rebecca M, Palliser Hannah K, Lakkundi Anil, de Waal Koert, Latter Joanna L, Clifton Vicki L, Wright Ian M R
Mothers and Babies Research Centre, Hunter Medical Research Institute, Newcastle, NSW, Australia (R.M.D., H.K.P., J.L.L., I.R.W.) Discipline of Paediatrics and Child Health, School of Medicine and Public Health, University of Newcastle, Newcastle, NSW, Australia (R.M.D., J.L.L., I.R.W.) Graduate School of Medicine and Illawarra Health and Medical Research Institute, University of Wollongong, Wollongong, NSW, Australia (R.M.D., I.R.W.).
Mothers and Babies Research Centre, Hunter Medical Research Institute, Newcastle, NSW, Australia (R.M.D., H.K.P., J.L.L., I.R.W.) School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, NSW, Australia (H.K.P.).
Physiol Rep. 2014 Sep 17;2(9):e12145. doi: 10.14814/phy2.12145.
Dysfunction of the transition from fetal to neonatal circulatory systems may be a major contributor to poor outcome following preterm birth. Evidence exists in the human for both a period of low flow between 5 and 11 h and a later period of increased flow, suggesting a hypoperfusion-reperfusion cycle over the first 24 h following birth. Little is known about the regulation of peripheral blood flow during this time. The aim of this study was to conduct a comparative study between the human and guinea pig to characterize peripheral microvascular behavior during circulatory transition. Very preterm (≤28 weeks GA), preterm (29-36 weeks GA), and term (≥37 weeks GA) human neonates underwent laser Doppler analysis of skin microvascular blood flow at 6 and 24 h from birth. Guinea pig neonates were delivered prematurely (62 day GA) or at term (68-71 day GA) and laser Doppler analysis of skin microvascular blood flow was assessed every 2 h from birth. In human preterm neonates, there is a period of high microvascular flow at 24 h after birth. No period of low flow was observed at 6 h. In preterm animals, microvascular flow increased after birth, reaching a peak at 10 h postnatal age. Blood flow then steadily decreased, returning to delivery levels by 24 h. Preterm birth was associated with higher baseline microvascular flow throughout the study period in both human and guinea pig neonates. The findings do not support a hypoperfusion-reperfusion cycle in the microcirculation during circulatory transition. The guinea pig model of preterm birth will allow further investigation of the mechanisms underlying microvascular function and dysfunction during the initial extrauterine period.
胎儿循环系统向新生儿循环系统过渡的功能障碍可能是早产预后不良的主要原因。在人类中,有证据表明出生后5至11小时存在一段低流量期,随后是流量增加期,这表明出生后的头24小时存在低灌注-再灌注循环。目前对这段时间外周血流的调节知之甚少。本研究的目的是在人类和豚鼠之间进行比较研究,以表征循环过渡期间外周微血管的行为。极早产儿(≤28周孕龄)、早产儿(29 - 36周孕龄)和足月儿(≥37周孕龄)在出生后6小时和24小时接受皮肤微血管血流的激光多普勒分析。豚鼠新生儿早产(62天孕龄)或足月出生(68 - 71天孕龄),并在出生后每2小时评估一次皮肤微血管血流的激光多普勒分析。在人类早产儿中,出生后24小时存在一段高微血管血流期。6小时时未观察到低流量期。在早产动物中,微血管血流在出生后增加,在出生后10小时达到峰值。然后血流稳步下降,到24小时时恢复到分娩时的水平。在整个研究期间,早产在人类和豚鼠新生儿中均与较高的基线微血管血流相关。这些发现不支持循环过渡期间微循环中的低灌注-再灌注循环。早产豚鼠模型将有助于进一步研究宫外初期微血管功能和功能障碍的潜在机制。