Rho-kinase inhibition attenuates acute hypoxic fetoplacental vasoconstriction in the rat

• Published in: Physiological research Vol. 61 Suppl 2; pp. S43 - S48
• Main Authors: Kafka, P, Vajnerová, O, Herget, J, Hampl, V
• Format: Journal Article
• Language: English
• Published: Czech Republic Institute of Physiology 01-01-2012
• Subjects: Animals; Calcium; Cells; Female; Fetuses; Hypoxia; Hypoxia - metabolism; Hypoxia - physiopathology; Laboratory animals; Muscular system; Phosphorylation; Placenta - blood supply; Placental Circulation - physiology; Pregnancy; Proteins; Rats; Rats, Wistar; rho-Associated Kinases - antagonists & inhibitors; rho-Associated Kinases - metabolism; Rodents; Smooth muscle; Vascular Resistance - physiology; Vasoconstriction - physiology; Czech Republic
• ISSN: 0862-8408; 1802-9973
• DOI: 10.33549/physiolres.932398

The vessels on the fetal side of the placenta differ from most other vascular beds except the lungs in that they respond to acute hypoxia by vasoconstriction. An essential role of calcium influx in the mechanism of this hypoxic fetoplacental vasoconstriction (HFPV) has been shown previously. That finding does not, however, exclude the possible involvement of other mechanisms of vascular tone regulation. In this study we tested the hypothesis that Rho-kinase-mediated calcium sensitization is involved in HFPV. We used a model of isolated rat placenta dually perfused (from both the maternal and fetal side) with Krebs salt solution saturated with normoxic and hypoxic gas mixture respectively at constant flow rate. Rho-kinase pathway was inhibited by fasudil (10 microM). We found that fasudil reduced basal normoxic fetoplacental vascular resistance and completely prevented HFPV. This suggests that the activity of Rho-kinase signaling pathway is essential for HFPV.