Effect of inhaled heparin on allergen-induced early and late asthmatic responses in patients with atopic asthma.

Heparin possesses anti-inflammatory properties, which appeared to be dependent on the dose, timing, and the route of administration in animal studies. In asthma, a single dose of inhaled heparin only slightly reduced the early asthmatic response (EAR) but failed to protect against the late asthmatic response (LAR) to inhaled allergen. We studied the effect of multiple doses of inhaled heparin on the EAR and LAR to inhaled house-dust mite extract in eight stable asthmatics in a two-period, randomized, double-blind, crossover study. During both study periods, a standardized allergen challenge was performed and PC20 histamine was measured 24 h before and 24 h postallergen. Five doses of unfractionated heparin sodium (1,000 U/kg/dose) or placebo were inhaled 90 and 30 min preallergen, and 2, 4, and 6 h postallergen. Airway response was measured by FEV1, and the EAR (0-3 h) and LAR (3-10 h) were expressed as corresponding areas under the time-response curves (AUC). The acute effects of heparin and placebo on baseline FEV1 were not different (p > 0.07). Although not reaching significance, heparin attenuated the EAR by an average of 40% (mean AUC(0-3) +/- SEM: 29.5 +/- 6.0 [placebo] and 17.8 +/- 5.5% fall x h [heparin]; p = 0.08), while it significantly reduced the LAR by an average of 36% (AUC(3-10) +/- SEM: 169.3 +/- 20.0 [placebo] and 109.1 +/- 23.6% fall x h [heparin]; p = 0.005). We conclude that inhaled heparin reduces the LAR to allergen in asthmatic subjects, which may be due to its anti-inflammatory activity. Our finding suggests that heparin may have potential as anti-asthma therapy.

[1]  P. O'Byrne,et al.  Reproducibility of allergen-induced early and late asthmatic responses. , 1995, The Journal of allergy and clinical immunology.

[2]  W. Mitzner,et al.  Role of cationic proteins in the airway. Hyperresponsiveness due to airway inflammation. , 1994, American journal of respiratory and critical care medicine.

[3]  D. Postma,et al.  Early and late asthmatic reaction after allergen challenge. , 1994, Respiratory medicine.

[4]  T. Ahmed,et al.  Preventing bronchoconstriction in exercise-induced asthma with inhaled heparin. , 1993, The New England journal of medicine.

[5]  C. Page,et al.  The effect of heparin and related proteoglycans on allergen and PAF-induced eosinophil infiltration. , 1993, Journal of lipid mediators.

[6]  T. Ahmed,et al.  Inhibition of antigen-induced airway and cutaneous responses by heparin: a pharmacodynamic study. , 1993, Journal of applied physiology.

[7]  S. Anderson,et al.  Airway responsiveness : standardized challenge testing with pharmacological, physical and sensitizing stimuli in adults , 1993 .

[8]  J E Cotes,et al.  Lung volumes and forced ventilatory flows. Report Working Party Standardization of Lung Function Tests, European Community for Steel and Coal. Official Statement of the European Respiratory Society. , 1993, The European respiratory journal. Supplement.

[9]  A. Fryer,et al.  Function of pulmonary M2 muscarinic receptors in antigen-challenged guinea pigs is restored by heparin and poly-L-glutamate. , 1992, The Journal of clinical investigation.

[10]  T. Ahmed,et al.  Immunologic mast cell-mediated responses and histamine release are attenuated by heparin. , 1992, Journal of applied physiology.

[11]  T. Ahmed,et al.  Effects of inhaled heparin on immunologic and nonimmunologic bronchoconstrictor responses in sheep. , 1992, The American review of respiratory disease.

[12]  A. B. Kay,et al.  Asthma and inflammation. , 1991, The Journal of allergy and clinical immunology.

[13]  S. Durham The significance of late responses in asthma , 1991, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[14]  Douglas G. Altman,et al.  Practical statistics for medical research , 1990 .

[15]  S. Durham,et al.  Leukocytes and mediators in bronchoalveolar lavage during allergen-induced late-phase asthmatic reactions. , 1989, The American review of respiratory disease.

[16]  J. Mullaney,et al.  Competitive, reversible, and potent antagonism of inositol 1,4,5-trisphosphate-activated calcium release by heparin. , 1988, Journal of Biological Chemistry.

[17]  S. Wenzel,et al.  Activation of pulmonary mast cells by bronchoalveolar allergen challenge. In vivo release of histamine and tryptase in atopic subjects with and without asthma. , 1988, The American review of respiratory disease.

[18]  P. O'Byrne,et al.  Allergen-induced airway hyperresponsiveness. , 1988, The Journal of allergy and clinical immunology.

[19]  P. Sterk,et al.  Maximal airway narrowing to inhaled leukotriene D4 in normal subjects. Comparison and interaction with methacholine. , 1987, The American review of respiratory disease.

[20]  L. Schwartz,et al.  Regulation of tryptase from human lung mast cells by heparin. Stabilization of the active tetramer. , 1986, The Journal of biological chemistry.

[21]  Ö. Hägermark,et al.  Inhibition of complement dependent experimental inflammation in human skin by different heparin fractions. , 1986, International journal of immunopharmacology.

[22]  A. Eldor,et al.  The Inhibitory Effect of Heparin and Related Glycosaminoglycans on Neutrophil Chemotaxis , 1984, Thrombosis and Haemostasis.

[23]  L. Jaques Heparins--anionic polyelectrolyte drugs. , 1979, Pharmacological reviews.

[24]  L. Jaques,et al.  INTRAPULMONARY HEPARIN A New Procedure for Anticoagulant Therapy , 1976, The Lancet.

[25]  E. Bardana,et al.  Heparin as treatment for bronchospasm of asthma. , 1969, Annals of allergy.

[26]  O. B. Williams,et al.  Further Studies on the Influence of Heparin on Anaphylactic Shock in the Guinea Pig , 1928, The Journal of Immunology.