Hypertension, Vol 8, 167-173, Copyright © 1986 by American Heart Association
AJ Woittiez, GJ Wenting, AH van den Meiracker, HJ Ritsema van Eck, AJ Man in't Veld, FA Zantvoort and MA Schalekamp
Ketanserin, an antagonist highly selective for 5-hydroxytryptamine
(serotonin) type 2 (S2) receptors, was given as monotherapy in a dose of 40
mg b.i.d. to 24 subjects with mild to moderate essential hypertension. Its
effects were evaluated in a placebo-controlled double- blind crossover
study. The effect on blood pressure in 18 subjects was monitored by 24-hour
ambulatory intra-arterial measurements. Systolic and diastolic
intra-arterial pressures were significantly lowered by ketanserin both
during the day and at night, whereas heart rate was unchanged. Cuff
pressure readings (triplicate measurements) with the London School of
Hygiene sphygmomanometer and an automatic device (12 measurements in 1
hour) in the outpatient clinic also showed a significant effect on both
supine and standing pressures. No postural hypotension was noted.
Ketanserin had no effect on endogenous creatinine clearance, serum
cholesterol levels, and the plasma levels of norepinephrine, renin, and
aldosterone. The only side effect that was significantly more common with
ketanserin than with placebo treatment was an increase in body weight.
Ketanserin may have a place in the treatment of mild to moderate essential
hypertension.
ARTICLES
Chronic effect of ketanserin in mild to moderate essential hypertension
This article has been cited by other articles:
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D. Wellens, G. Peeters, B. Baeten, G. Sieben, and J. Symoens Double-Blind Comparison of Ketanserin with Placebo in Patients with Essential Hypertension Angiology, November 1, 1986; 37(11): 810 - 817. [Abstract] [PDF] |
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