Why the study?
Does indapamide reduce blood pressure and alter vascular reactivity in experimental hypertensive animal models?
Does indapamide reduce blood pressure and alter vascular reactivity in experimental hypertensive animal models?
Indapamide demonstrates a hypotensive effect and reduces vascular reactivity to sympathetic stimulation in hypertensive animal models, suggesting a direct vascular mechanism of action.
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Indapamide may exert direct vascular effects in hypertensive animal models; hypothesis-generating and should not yet change clinical practice.
SummaryIndapamide (13 mg to 16 mg/kg p.o.) produced a fall in blood pressure in conscious renal hypertensive cats without any reflex tachycardia. Repeated administration of indapamide for 2 weeks effected a well maintained reduction in blood pressure. Furthermore, the hypotensive effect of clonidine (20μg i.c.v.) was enhanced 1 week after completion of treatment with indapamide, suggesting a long-lasting effect of indapamide. In experimental hypertensive rats, indapamide (10 mg/kg p.o.) lowered blood pressure (40 mmHg) recorded directly from an in-dwelling catheter and the effect was maintained for 24 hours. In DOCA-saline hypertensive rats, 10-days' treatment with indapamide (10 mg/kg p.o.) or hydrochlorothiazide (5 mg/kg i.p.) produced falls in blood pressure of similar magnitude, as measured by an indirect method. Vasopressor effects induced by i.v. noradrenaline, 5-HT, tyramine or by stimulation of the entire sympathetic outflow were significantly reduced by indapamide pre-treatment but not by hydrochlorothiazide. Vascular reactivity of isolated rat mesentery preparations to noradrenaline, 5-HT and ATP was not reduced by indapamide pre-treatment but such treatment did reduce the frequency of spontaneous contractions in isolated rat portal vein preparations. The results suggest a vascular site of action for indapamide.
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Finch et al. (1977) studied this question.
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