4.3 Article

Why is human uterine artery blood flow during pregnancy so high?

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpregu.00167.2022

关键词

fetal growth; hypoxia; nutrient delivery

资金

  1. National Institutes of Health [HD088590, HL138181, HL 079647, TW007957, DK108910]
  2. Action Medical Research [SP4545]
  3. British Heart Foundation [PS/02/002/14893, RG/07/004/22659]

向作者/读者索取更多资源

In healthy near-term women, blood flow to the uteroplacental circulation is greater than in other mammals, and this high blood flow plays a crucial role in maintaining normal fetal growth. Populations living at high altitudes have higher levels of uterine artery blood flow and exhibit normal fetal growth, while newcomers experience slower fetal growth.
In healthy near-term women, blood flow to the uteroplacental circulation is estimated as 841 mL/min, which is greater than in other mammalian species. We argue that as uterine venous Po-2 sets the upper limit for O-2 diffusion to the fetus, high uterine artery blood flow serves to narrow the maternal arterial-to-uterine venous Poe gradient and thereby raise uterine vein Po-2. In support, we show that the reported levels for uterine artery blood flow agree with what is required to maintain normal fetal growth. Although residence at high altitudes (>2,500 m) depresses fetal growth, not all populations are equally affected; Tibetans and Andeans have higher levels of uterine artery blood flow than newcomers and exhibit normal fetal growth. Estimates of uterine venous Po-2 from the umbilical blood-gas data available from healthy Andean pregnancies indicate that their high levels of uterine artery blood flow are consistent with their reported, normal birth weights. Unknown, however, are the effects on placental gas exchange of the lower levels of uterine artery blood flow seen in high-altitude newcomers or hypoxia-associated pregnancy complications. We speculate that, by widening the maternal artery to uterine vein Po-2 gradient, lower levels of uterine artery blood flow prompt metabolic changes that slow fetal growth to match O-2 supply.

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