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Am J Physiol Heart Circ Physiol ; 282(3): H918-25, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11834487

ABSTRACT

Genetically altered mice may provide useful models for exploring cardiovascular regulation during pregnancy and postpartum if changes in mice mimic humans. We found in awake ICR (CD-1) mice at 17.5 days gestation that hematocrit was reduced 18%, and the pressor response to intravenous angiotensin II was reduced ~33%. Arterial pressure in awake mice was 12% lower in early pregnancy (3.5 days) than late pregnancy (17.5 days) and postpartum (3 and 17 days after delivery), whereas heart rate was 10-20% higher in the peripartum period (17.5 days gestation and 3 days postpartum). In late pregnancy, cardiac output under isoflurane anesthesia was 64% higher than in nonpregnant mice, due to a 37% increase in stroke volume and a 17% increase in heart rate. All changes P < 0.05. We conclude that, as in humans, mice exhibit hypotension in early pregnancy, and a blunted pressor response to angiotensin II, a decrease in hematocrit, and a marked increase in cardiac output in late pregnancy.


Subject(s)
Cardiovascular Physiological Phenomena , Hemodynamics/physiology , Postpartum Period/physiology , Pregnancy, Animal/physiology , Animals , Blood Flow Velocity , Blood Pressure , Cardiac Output , Female , Heart Rate , Hematocrit , Mice , Mice, Inbred ICR , Pregnancy , Reference Values , Stroke Volume
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