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Endothelium-Dependent Potentiation by Cocaine of Serotonin-Induced Contractions in Sheep Fetal Umbilical ArteryCenter fo Perinatal Biology, Department of Pharmacology, Lonta Linda University School of Medicine, Lonta Linda, California; lzhang{at}ccmail.liu.edu
Center fo Perinatal Biology, Department of Pharmacology, Lonta Linda University School of Medicine, Lonta Linda, California Objective: To evaluate the potential role of the endothelium in cocaine-mediated potentiation of serotonin-induced contractions of fetal ovine umbilical artery. Methods: Umbilical cords were isolated from near-term pregnant ewes (approximately 140 days). Serotonin-induceddose-dependent contraction of the umbilical arteries was performed in the presence and absence of 3 µmol/L cocaine. The responses were compared before and after removal of the endothelium.
Results: Cocaine (3 µmol/L) potentiated serotonin-induced contractions in the endothelium-intact ovine fetal umbilical arteries and shifted the concentration-response curve to the left (median effective concentration: 2.69 ± 0.11 Conclusion: The results suggest that, in ovine fetal umbilical arteries, cocaine-mediated potentiation of serotonin-induced contractions is endothelium dependent.
Key Words: Cocaine serotonin umbilical artery (sheep) endothelium
Journal of the Society for Gynecologic Investigation, Vol. 5, No. 2,
72-74 (1998) |
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1.23 ± 0.14 µmol/L, P < .01). The maximum response expressed as a percentage of maximum KCl was also significantly increased (167.4 ± 12.8 