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pubmed-article:7959319pubmed:abstractTextThe umbilical-placental circulation is of vital importance for fetal survival and has a dominant effect on the cardiorespiratory physiology of the fetus. The mechanisms of regulation of umbilical vessels appear to differ from those regulating other vessels. Both clonidine and alpha-methyldopa have been used in the management of hypertensive complications of pregnancy. In contrast to alpha-methyldopa, clonidine does not require previous metabolization but acts directly on the receptors. The action of the two drugs on human umbilical artery was studied in vitro. Forty-eight human umbilical artery segments were dissected and perfused as follows: 9 segments with alpha-methyldopa, 10 with clonidine, 10 with yohimbine, 9 with alpha-methyldopa in combination with yohimbine, and 10 with pure Tyrode's solution. alpha-Methyldopa had a statistically significant vasoconstrictive effect starting at 40 min (p < 0.05) and this effect was blocked by yohimbine (p < 0.05). Clonidine had no vasoconstrictive effect. The present data for clonidine do not confirm the presence of alpha 2-adrenergic receptors in the umbilico-placental circulation which had been indicated by the action of methyldopa.lld:pubmed
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pubmed-article:7959319pubmed:authorpubmed-author:FrançaL CLClld:pubmed
pubmed-article:7959319pubmed:authorpubmed-author:CastroR MRMlld:pubmed
pubmed-article:7959319pubmed:authorpubmed-author:CunhaS PSPlld:pubmed
pubmed-article:7959319pubmed:authorpubmed-author:NagataN YNYlld:pubmed
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pubmed-article:7959319pubmed:volume38lld:pubmed
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pubmed-article:7959319pubmed:pagination18-20lld:pubmed
pubmed-article:7959319pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:7959319pubmed:year1994lld:pubmed
pubmed-article:7959319pubmed:articleTitleIn vitro study of the effect of clonidine on human umbilical artery motility.lld:pubmed
pubmed-article:7959319pubmed:affiliationDepartment of Gynecology and Obstetrics, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Brazil.lld:pubmed
pubmed-article:7959319pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7959319pubmed:publicationTypeComparative Studylld:pubmed
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