Calcium Antagonistic Agent
نویسندگان
چکیده
Hemodynamic monitoring after a single dose (10 mg) of nifedipine in 27 primary hypertensive subjects (diastolic pressure > 110 mm Hg) documented that this calcium antagonistic agent exerts a potent arteriolar vasodilating action, which results in prompt (-21% of control at 30 minutes) and persistent (-16% of control at 120 minutes) fall in mean arterial pressure associated with a rise in cardiac output and pulse rate. The same patients received oral treatment for 3 weeks. Hourly pressure readings showed that 1) the antihypertensive response to each dose lasts 8-12 hours; and 2) nifedipine every 6 hours significantly reduced blood pressure throughout the 24 hours, without postural hypotension. Side effects were short-lasting (headache in five patients, palpitation without arrhythmias in eight patients, burning sensation in the face and legs in five patients and sporadic extrasystoles in five patients) and tended to disappear with continued treatment. Development of drug resistance, sodium retention, plasma volume expansion, renin release or angina pectoris were not observed during the study. Although these findings seem to differentiate nifedipine from other vasodilators currently used in the treatment of hypertension, broader experience and more prolonged trials with nifedipine as an antihypertensive agent will be needed before conclusions can be drawn on these particular aspects.
منابع مشابه
Antagonistic Activity of Fructoplane Yeast Against Ulocladium Rot of Papaya
Debaryomyces hanseniZopf isolated from the fructoplane of apples were found to be effective as biocontrol agent against rot of papaya caused by Ulocladium. chartarum(Pr.) Simm. The ability of D. hansenii to prevent infection of U. chartarum was lost when the antagonist cells were killed by autoclaving. Cell free culture filtrates of antagonist were unable to prevent disease incidence. Efficacy ...
متن کاملCalcium Antagonistic Activity of Biophytum Petersianum on Vascular Smooth Muscles of Wistar Rat
The whole plant of Biophytum petersianum was extracted with a mixture of water – alcohol (1:1) to evaluate its relaxant effect on aorta rings. In isolated Wistar rat tissue, the hydro-ethanolic extract (0.1; 0.25 and 0.5 mg/ml) non-competitively antagonized calcium chloride and high-K + - induced aorta contractions in a concentration-dependent manner. Moreover, the inhibition of noradr...
متن کاملIN VITRO ANTAGONISTIC EFFECTS OF TRICHODERMA SPP. ON SEVERAL SOILBORNE PLANT PATHOGENIC FUNGI
In vitro studies with Trichoderma spp., soil-borne fungal antagonists, demonstrated that a number of isolates produced volatile and non-volatile metabolites capable of inhibiting the growth and sporulation of several soil-borne plant pathogenic fungi. Microscopic observations showed that T. harzianm and T. viride, isolated from soil samples from Ahwaz and Karaj, adversely affected the myce...
متن کاملDrug therapy of urinary urge incontinence: a systematic review.
OBJECTIVE To review the efficacy of drug therapy for urinary urge incontinence by examining the published literature. METHODS OF STUDY SELECTION In October 1999, we searched the medical databases MEDLINE, EMBASE, and Cochrane Controlled Trials Register to identify prospective randomized, double-blind, placebo-controlled clinical trials in the English literature evaluating drug therapy (except...
متن کاملStudy of Antagonistic Effects of Trichoderma Species on Growth of Verticillium dahliae, the Causal Agent of VerticilliumWilt of Pistachio under Laboratory Condition
Verticillium wilt is a serious disease of pistachio caused by Verticilliumdahliae. Control of the disease is difficult due to soil borne nature of the causal agent. Verticillium wilt has been biologically controlled by Trichoderma spp. In the present study, Trichoderma spp. was isolated from soils of pistachio orchards and their effect was investigated on radial growth of Verticillium dahliae b...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2005