Inhibitory effects of beta-adrenergic stimulants on increased vascular permeability caused by passive cutaneous anaphylaxis, allergic mediators, and mediator releasers in rats

Pharmacology. 1989;39(1):19-27. doi: 10.1159/000138567.

Abstract

The effects of isoproterenol, salbutamol, theophylline, and forskolin on IgE antibody-mediated homologous passive cutaneous anaphylaxis (PCA) and on skin reactions caused by allergic mediators and mediator releasers were investigated in rats. Isoproterenol and salbutamol dose-dependently inhibited the PCA and skin reactions caused by histamine, serotonin, and leukotriene C4 (LTC4), elicited at the same time in the same rat. These agents also dose-dependently inhibited the skin reactions caused by platelet-activating factor (PAF), leukotriene D4 (LTD4), compound 48/80 (48/80), and calcium ionophore A23187 (A23187). Propranolol overcame the inhibitory effect of isoproterenol on PCA and skin reactions in a dose-dependent manner. Theophylline and forskolin showed similar effects as the beta-adrenergic stimulants. These results indicate that beta-adrenergic stimulants inhibit the increased vascular permeability caused by allergic mediators, and suggest that this activity of beta-adrenergic stimulants might play an important role in their antiallergic actions. Inhibition of increased vascular permeability might be mediated via beta-receptors and may be related to the increase in intracellular cyclic AMP levels.

MeSH terms

  • Adrenergic beta-Agonists / pharmacology*
  • Albuterol / pharmacology
  • Animals
  • Ascaris / immunology
  • Capillary Permeability / drug effects*
  • Colforsin / pharmacology
  • Cyclic AMP / metabolism
  • Female
  • Histamine Release / drug effects
  • Hypersensitivity / metabolism
  • Hypersensitivity / physiopathology*
  • Immunoglobulin E / immunology
  • Isoproterenol / pharmacology
  • Passive Cutaneous Anaphylaxis / drug effects*
  • Rats
  • Rats, Inbred Strains
  • Skin / physiopathology
  • Theophylline / pharmacology

Substances

  • Adrenergic beta-Agonists
  • Colforsin
  • Immunoglobulin E
  • Theophylline
  • Cyclic AMP
  • Isoproterenol
  • Albuterol