Literature DB >> 5315684

Inhibitory effects of aprotinin on kallikrein and kininases in dog's blood.

S M Pojda, J R Vane.   

Abstract

1. The blood-bathed organ technique was used in dogs to estimate kinin generation in the blood. Strips of cat jejunum were used as assay tissues.2. Infusions of kallikrein at 0.5-8 mU / ml into the blood in the extracorporeal circuit led to a generation of kinin at 0.6-10 ng / ml. The kinin generated was at the same concentration after incubation of kallikrein with blood for 15 s or 120 seconds. Intravenous infusions of kallikrein at (8-125 mU / kg) / min led to similar blood concentrations of kinin. These infusions induced substantial falls in blood pressure.3. Aprotinin inhibited the generation of kinin by kallikrein, but the concentration needed in vivo was 20,000 times higher than would be expected from the definition of the units.4. After intravenous injection of large doses of aprotinin, the kallikrein-inhibiting activity passed off within 40-60 minutes. At the same time, there was a gradual reduction in kininase activity, so that the half life of bradykinin in blood increased from a mean of 13 s to 40 seconds. This effect reached a maximum 1-3 h after injection of aprotinin.5. It is suggested that a metabolite of aprotinin is responsible for the kininase inhibition and that this effect may limit the usefulness of aprotinin in man.

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Year:  1971        PMID: 5315684      PMCID: PMC1665766          DOI: 10.1111/j.1476-5381.1971.tb07140.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  9 in total

1.  THE USE OF ISOLATED ORGANS FOR DETECTING ACTIVE SUBSTANCES IN THE CIRCULATING BLOOD.

Authors:  J R VANE
Journal:  Br J Pharmacol Chemother       Date:  1964-10

2.  AN IN VIVO ESTIMATION OF THE POTENCIES AND HALF-LIVES OF SYNTHETIC BRADYKININ AND KALLIDIN.

Authors:  D A MCCARTHY; D E POTTER; E D NICOLAIDES
Journal:  J Pharmacol Exp Ther       Date:  1965-04       Impact factor: 4.030

3.  [On the esterase effects of kallikrein and trypsin and their inhibition by kallikrein-and trypsin inhibitors].

Authors:  E WERLE; B KAUFMANN-BOETSCH
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1960

4.  The detection and estimation of bradykinin in the circulating blood.

Authors:  S H Ferreira; J R Vane
Journal:  Br J Pharmacol Chemother       Date:  1967-03

5.  Release of additional factors in anaphylaxis and its antagonism by anti-inflammatory drugs.

Authors:  P J Piper; J R Vane
Journal:  Nature       Date:  1969-07-05       Impact factor: 49.962

Review 6.  The release and fate of vaso-active hormones in the circulation.

Authors:  J R Vane
Journal:  Br J Pharmacol       Date:  1969-02       Impact factor: 8.739

7.  The generation of kinins in the blood of dogs during hypotension due to haemorrhage.

Authors:  H E Berry; J G Collier; J R Vane
Journal:  Clin Sci       Date:  1970-09       Impact factor: 6.124

8.  Subcellular distribution and properties of the bradykinin inactivation system in rabbit brain homogenates.

Authors:  A C Camargo; F G Graeff
Journal:  Biochem Pharmacol       Date:  1969-02       Impact factor: 5.858

9.  The disappearance of bradykinin and eledoisin in the circulation and vascular beds of the cat.

Authors:  S H Ferreira; J R Vane
Journal:  Br J Pharmacol Chemother       Date:  1967-06
  9 in total
  2 in total

1.  Effects of tranexamic acid and aprotinin, two antifibrinolytic drugs, on PAF-induced plasma extravasation in unanesthetized rats.

Authors:  J G O'Brien; B Battistini; F Zaharia; G E Plante; P Sirois
Journal:  Inflammation       Date:  2000-10       Impact factor: 4.092

2.  The inactivation of bradykinin in the pulmonary circulation of isolated lungs.

Authors:  V A Alabaster; Y S Bakhle
Journal:  Br J Pharmacol       Date:  1972-06       Impact factor: 8.739

  2 in total

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