Subject(s)
Aprotinin/pharmacology , Kinins/blood , Pancreatic Extracts/pharmacology , Peptide Hydrolases/blood , Povidone/pharmacology , Vascular Resistance/drug effects , Animals , Blood Coagulation/drug effects , Drug Combinations/pharmacology , Fibrinolysin/metabolism , Fibrinolysis/drug effects , Kallikreins/blood , Rabbits , Thrombin/metabolismABSTRACT
The effects of kallikrein, thrombin, and plasmin on interaction of acetylcholine and noradrenaline with receptors of the isolated portal vein of guinea-pigs were studied. The functional activity of receptors was studied by the pharmacokinetic method. It was found that kallikrein and thrombin do not disturb the kinetics of agonist interaction with receptors, whereas the magnitude of isometric vascular contractions dramatically decreased after plasmin treatment and becomes disproportionate to the concentration of neurotransmitters. Exposure of the portal vein to kallikrein or thrombin caused different changes in the sensitivity and quantity of active cholino- and adrenoreceptors. These proteolytic enzymes reduced the sensitivity of receptors to noradrenaline and increased it to acetylcholine. Exposure to kallikrein brought about a decrease in the quantity of active cholinoreceptors and a rise in the number of adrenoreceptors. The treatment of the vessels with thrombin resulted in a decrease in the number of active adrenoreceptors. The number of active cholinoreceptors remained unchanged.
Subject(s)
Peptide Hydrolases/pharmacology , Receptors, Adrenergic/drug effects , Receptors, Cholinergic/drug effects , Animals , Dose-Response Relationship, Drug , Fibrinolysin/pharmacology , Guinea Pigs , In Vitro Techniques , Kallikreins/pharmacology , Muscle Contraction/drug effects , Muscle, Smooth, Vascular/drug effects , Peptide Hydrolases/blood , Portal Vein/drug effects , Thrombin/pharmacologySubject(s)
Bacterial Infections/therapy , Kallikreins/blood , Kinins/blood , Pneumonia/therapy , Protease Inhibitors/therapeutic use , Child, Preschool , Female , Fluid Therapy , Humans , Infant , MaleSubject(s)
Erythrocyte Aggregation , Kallikreins/physiology , Kinins/physiology , Mosaicism , Animals , Aorta/physiology , Carbon Tetrachloride Poisoning/physiopathology , Dogs , Epinephrine/pharmacology , Erythrocyte Aggregation/drug effects , Guinea Pigs , Hemostasis , Hepatectomy , Intestine, Small/physiology , Liver/drug effects , Liver/physiology , Lung/physiology , RatsSubject(s)
Kinins/blood , Pneumonia, Staphylococcal/blood , Animals , Child, Preschool , Disease Models, Animal , Humans , Infant , Kallikreins/blood , Kininogens/blood , Rabbits , Time FactorsABSTRACT
The equation describing kinetics of interaction between bradykinin and cardiovascular receptors resembles the equations describing depressive adrenergic and some cholinergic reactions in dogs, rabbits and white rats. In this study of bradykinin receptor state, in order to describe quantitatively hypotensive action of different bradykinin doses on interaction of this peptide with receptors, bradykinin had to be injected intraaortally. The data obtained revealed that the greatest efficiency of kininergic reaction occurred in dogs whereas the least--in white rats.