Terazosin: Ex vivo and in vitro platelet aggregation effects in patients with arterial hypertension

Antihypertensive effect, platelet aggregation, and plasma lipid profile were studied in a group of 14 hypertensive patients with diastolic blood pressure between 96 and 116 mm Hg during placebo and terazosin phases. Terazosin, an α 1-adrenergic blocking agent, was given initially at the dosage of 1...

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Published inAmerican journal of hypertension Vol. 9; no. 5; pp. 437 - 444
Main Authors Hernández, Rafael Hernández, Angeli-Greaves, Miriam, Carvajal, Atiff Rafael, Pajuelo, Jaime Guerrero, Armas Padilla, María Cristina, Armas-Hernández, María José
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.05.1996
Oxford University Press
Elsevier Science
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Summary:Antihypertensive effect, platelet aggregation, and plasma lipid profile were studied in a group of 14 hypertensive patients with diastolic blood pressure between 96 and 116 mm Hg during placebo and terazosin phases. Terazosin, an α 1-adrenergic blocking agent, was given initially at the dosage of 1 mg daily. Then it was continued at a dosage of 2 mg daily and 5 mg daily respectively, each dosage for 4 weeks. Blood pressure was taken every 2 weeks. Ex vivo platelet aggregation induced by epinephrine, collagen, and adenosine diphosphate (ADP) were carried out twice during the first placebo phase, once at the end of each terazosin dosage, and once in the second placebo phase. Total cholesterol, HDL cholesterol, and triglycerides were measured at the end of first placebo and terazosin phases. Blood from eight patients was taken during the second placebo phase to carry out in vitro response of platelet aggregation induced by ADP, collagen, and epinephrine before and after incubation with terazosin (1, 2 and 5 μg/L or doxazosin (100, 200, and 500 μg/L) for 5 min. Terazosin induced a statistically significant decrease in 14.2 8.0 mm Hg, 26.1 13.4 mm Hg, and 33.9 16.5 mm Hg in the supine position for 1, 2, and 5 mg/daily, respectively. No changes in heart rate were observed. Terazosin inhibited significant ex vivo platelet aggregation induced by epinephrine, collagen, and ADP in a range from 20% to 45% for different concentrations of inducers. Reductions in platelet aggregation seemed not to be dose dependent, as reductions were statistically equivalent for dosages of 1, 2, and 5 mg daily. Terazosin significantly reduced the level of total cholesterol (8.71%) and triglycerides (14.31%), and increased (although not significantly) levels of HDL cholesterol (3.91%). In vitro platelet aggregation was inhibited by doxazosin to a significant extent but not by terazosin.
Bibliography:href:9_5_437.pdf
istex:E96EA181876C3FADFC77F06A71F9D7D539CC01F5
Address correspondence and reprint requests to Dr. Rafael Hernández Hernández, Clinical Pharmacology Unit, School of Medicine, Universidad Centro Occidental Lisandro Alvarado, P.O. Box 400, 3001, Barquisimeto, Venezuela.
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ISSN:0895-7061
1879-1905
1941-7225
DOI:10.1016/0895-7061(95)00436-X