Effect of Ca2+ Agonist Bay K 8644 in human placental arteries

dc.contributor.authorBarrús, MT
dc.contributor.authorReviriego, J
dc.contributor.authorMarín, J
dc.date.accessioned2024-07-08T11:50:43Z
dc.date.available2024-07-08T11:50:43Z
dc.date.issued1995-09
dc.description.abstract1. Bay K 8644 (0.1 μM) induced weak contractions in human placental artery segments that were increased in the presence of 7.5 mM K+. K+ and serotonin (5-HT) induced contractions that were enhanced by preincubation of segments with Bay K 8644. These enhancements were reduced by nifedipine (0.1 μM) and diltiazem (1 μM). 2. Bay K 8644 induced a 45Ca2+ uptake increase which was potentiated by depolarization with K+ (less than 30 mM) and antagonized by nifedipine. K+ (15 and 30 mM) and 5-HT (1 μM) induced 45Ca2+ uptake that was enhanced by Bay K 8644. 3. These results suggest that Bay K 8644: (1) is unable to activate the quiescent potential-operated Ca2+ channels (POCs) of these arteries, and (2) activates receptor (5-HT)-operated Ca2+ channels or facilitates Ca2+ influx through POCs activated by 5-HT.es
dc.identifier.citationM.T. Barrús, J. Reviriego, J. Marin, Effect of Ca2+ Agonist Bay K 8644 in human placental arteries, General Pharmacology: The Vascular System, Volume 26, Issue 5, 1995, Pages 989-996, ISSN 0306-3623, https://doi.org/10.1016/0306-3623(94)00289-Y.es
dc.identifier.doi10.1016/0306-3623(94)00289-Yes
dc.identifier.issn0306-3623
dc.identifier.urihttps://hdl.handle.net/10115/37111
dc.language.isoenges
dc.publisherElsevieres
dc.rights.accessRightsinfo:eu-repo/semantics/closedAccesses
dc.subjectHuman placental arteriesBay K 8644nifedipinediltiazemcalcium channelses
dc.titleEffect of Ca2+ Agonist Bay K 8644 in human placental arterieses
dc.typeinfo:eu-repo/semantics/articlees

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