Literature DB >> 811997

Effects of phentolamine, dihydroergocristine and isoxsuprine on the blood pressure and heart rate in normotensive, hypotensive and hypertensive rats.

C Morpurgo, D Faini, A Falcone.   

Abstract

Phentolamine, dihydroergocristine and isoxsuprine were compared for their effects on the blood pressure in anaesthetized normotensive rats, in rats made hypotensive by ganglionic blockade or by pithing and in rats with noradrenaline-induced hypertension. Their ability to inhibit pressor responses elicited by electrical stimulation of the posterior hypothalamus and of the sympathetic outflow from the spinal cord was also investigated. All three drugs appeared very potent in inhibiting noradrenaline-induced hypertension and caused a dose-dependent fall in blood pressure in normotensive rats, which however was less pronounced with dihydroergocristine than with phentolamine and isoxsuprine. In hypotensive rats, dihydroergocristine caused a rise in blood pressure. At higher doses than those required to block noradrenaline-induced hypertension, the three drugs inhibited pressor responses elicited by electrical stimulation and were equally active on peripherally- and centrally-evoked responses. Simultaneous recording of heart rate and blood pressure, both in anaesthetized and in pithed rats, indicated a reflex origin for phentolamine-induced tachycardia and a direct cardiac stimulation for isoxsuprine. Reflex changes of heart rate were not observed with dihydroergocristine.

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Year:  1975        PMID: 811997     DOI: 10.1007/BF00499947

Source DB:  PubMed          Journal:  Naunyn Schmiedebergs Arch Pharmacol        ISSN: 0028-1298            Impact factor:   3.000


  13 in total

1.  The pharmacology of catecholamines and their derivatives. I. Relationship between structure and activity especially as far as the vascular system is concerned.

Authors:  E J ARIENS; M J WAELEN; P F SONNEVILLE; A M SIMONIS
Journal:  Arzneimittelforschung       Date:  1963-07

2.  A survey of the effects of isoxsuprine on nonvascular smooth muscle.

Authors:  P M LISH; K W DUNGAN; E L PETERS
Journal:  J Pharmacol Exp Ther       Date:  1960-06       Impact factor: 4.030

3.  [Pharmacology of a new vasodilator drug of the p-hydroxy ephedrine series].

Authors:  F BRUCKE; G HERTTING; A LINDNER; M LOUDON
Journal:  Wien Klin Wochenschr       Date:  1956-03-16       Impact factor: 1.704

4.  Investigations on the hypotensive effect of the hydrogenated ergot alkaloids.

Authors:  H KONZETT; E ROTHLIN
Journal:  Br J Pharmacol Chemother       Date:  1953-06

5.  A pithed rat preparation suitable for assaying pressor substances.

Authors:  R E SHIPLEY; J H TILDEN
Journal:  Proc Soc Exp Biol Med       Date:  1947-04

6.  The pharmacology of the natural and dihydrogenated alkaloids of ergot.

Authors:  E ROTHLIN
Journal:  Bull Schweiz Akad Med Wiss       Date:  1947-03

7.  Effects of sympathetic and central nervous system alterations on the blood pressure responses to phentolamine.

Authors:  C C Hilliard; E E Bagwell; H B Daniell
Journal:  J Pharmacol Exp Ther       Date:  1972-03       Impact factor: 4.030

8.  Some new vascular and biochemical aspects of the mechanism of action of ergot compounds.

Authors:  B Berde
Journal:  Headache       Date:  1972-01       Impact factor: 5.887

9.  A method of stimulating the complete sympathetic outflow from the spinal cord to blood vessels in the pithed rat.

Authors:  J S Gillespie; T C Muir
Journal:  Br J Pharmacol Chemother       Date:  1967-05

10.  Myocardial and haemodynamic effects of phentolamine.

Authors:  P K Das; J R Parratt
Journal:  Br J Pharmacol       Date:  1971-03       Impact factor: 8.739

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  1 in total

1.  Uncoupling of cerebral blood flow and glucose utilization by dihydroergocristine in the conscious rat.

Authors:  T Beck; P Vogg; J Krieglstein
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1988-07       Impact factor: 3.000

  1 in total

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