Anti-hypertensive therapy and the feto-placental circulation: effects on umbilical artery resistance

Verfasser / Beitragende:
[D.D. Houlihan, M.C. Dennedy, N. Ravikumar, J.J. Morrison]
Ort, Verlag, Jahr:
2004
Enthalten in:
Journal of Perinatal Medicine, 32/4(2004-07-09), 315-319
Format:
Artikel (online)
ID: 378938096
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024 7 0 |a 10.1515/JPM.2004.058  |2 doi 
035 |a (NATIONALLICENCE)gruyter-10.1515/JPM.2004.058 
245 0 0 |a Anti-hypertensive therapy and the feto-placental circulation: effects on umbilical artery resistance  |h [Elektronische Daten]  |c [D.D. Houlihan, M.C. Dennedy, N. Ravikumar, J.J. Morrison] 
520 3 |a Objective: To investigate and compare the direct effects of compounds used in the treatment of hypertensive disease in pregnancy on human umbilical artery resistance in vitro. Methods: Isometric tension recordings were performed under physiological conditions on human umbilical arterial rings (n=30). The in vitro effects of labetolol, hydralazine, alpha-methyldopa, nifedepine and magnesium sulphate (at concentration ranges from 1 nanomolar to 1 millimolar), and their respective vehicle controls, were measured. Results were expressed as −logEC50 (pD2) and mean maximal inhibition values for each compound. Results: All compounds investigated, except alpha methyldopa, exerted a significant relaxant effect on umbilical arterial tone. Alpha-methyldopa was significantly less potent when compared to all other compounds (mean maximal inhibition value [20.89±7.99%] versus all other agents [range 63.15±8.70−84.12±3.84%] (P<0.01)). The dose response curve of nifedipine yielded a significantly greater pD2 value when compared to that of hydralazine, labetalol, and magnesium sulphate (pD2 value [5.82±0.34] versus the above groups [range 3.10±0.09−3.52±0.14] (P<0.01)). Conclusion: These findings demonstrate that agents commonly used for the treatment of hypertensive disease in pregnancy, excluding alpha-methyldopa, have significant direct effects on the feto-placental circulation. These results suggest that alpha-methyldopa administration during pregnancy is less likely to produce significant direct effects on fetal vasculature then other agents used. 
540 |a Copyright © 2004 by Walter de Gruyter GmbH & Co. KG 
690 7 |a Human reproduction, growth & development  |2 nationallicence 
690 7 |a Gynaecology & obstetrics  |2 nationallicence 
690 7 |a Paediatric medicine  |2 nationallicence 
700 1 |a Houlihan  |D D.D.  |4 aut 
700 1 |a Dennedy  |D M.C.  |4 aut 
700 1 |a Ravikumar  |D N.  |4 aut 
700 1 |a Morrison  |D J.J.  |4 aut 
773 0 |t Journal of Perinatal Medicine  |d Walter de Gruyter  |g 32/4(2004-07-09), 315-319  |x 0300-5577  |q 32:4<315  |1 2004  |2 32  |o jpme 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Dennedy  |D M.C.  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ravikumar  |D N.  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Morrison  |D J.J.  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Journal of Perinatal Medicine  |d Walter de Gruyter  |g 32/4(2004-07-09), 315-319  |x 0300-5577  |q 32:4<315  |1 2004  |2 32  |o jpme 
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