H1-antihistamines and oxidative burst of professional phagocytes.

OBJECTIVES We analysed and compared the effect of five H1-antihistamines on stimulated oxidative burst at extra- and intracellular level of isolated and stimulated human polymorphonuclear leukocytes. DESIGN Oxidative burst of isolated human neutrophils was studied by means of luminol and isoluminol enhanced chemiluminescence. RESULTS The following rank order of potency for H1-antihistamines to decrease chemiluminescence was evaluated extracellularly: dithiaden> loratadine> chlorpheniramine> brompheniramine> pheniramine and at intracellular site: loratadine> dithiaden. CONCLUSION H1-antihistamines differ substantially according to their chemical structure in suppressing oxidative burst both at extra- and intracellular site of isolated stimulated human neutrophils.

[1]  K. Bauerová,et al.  Decreased activity of neutrophils in the presence of diferuloylmethane (curcumin) involves protein kinase C inhibition. , 2009, European journal of pharmacology.

[2]  A. Lojek,et al.  Inhibition of superoxide generation and myeloperoxidase release by carvedilol after receptor and nonreceptor stimulation of human neutrophils. , 2008, Neuro - endocrinology letters.

[3]  P. Denev,et al.  Comparative investigations of the influence of H1-antihistamines on the generation of reactive oxygen species by phagocytes , 2008, Inflammation Research.

[4]  K. Drábiková,et al.  Extra- and intracellular formation of reactive oxygen species by human neutrophils in the presence of pheniramine, chlorpheniramine and brompheniramine. , 2006, Neuro endocrinology letters.

[5]  L. Račková,et al.  The combined luminol/isoluminol chemiluminescence method for differentiating between extracellular and intracellular oxidant production by neutrophils , 2006, Redox report : communications in free radical research.

[6]  L. Račková,et al.  Antiradical effects of antihistamines in human blood. Structure-activity relationship. , 2006, Inflammation Research.

[7]  T. Mačičková,et al.  Extra- and intracellular oxidant production in phorbol myristate acetate stimulated human polymorphonuclear leukocytes: modulation by histamine and H1-antagonist loratadine , 2006, Inflammation Research.

[8]  M. Číž,et al.  Effect of H1-antihistamines on the oxidative burst of rat phagocytes , 2006, Inflammation Research.

[9]  K. Drábiková,et al.  Antiplatelet and antiphagocyte activity of H1-antihistamines , 2005, Inflammation Research.

[10]  M. Číž,et al.  Effect of H1-antagonist Dithiaden® on human PMN-leukocyte aggregation and chemiluminescence is stimulus-dependent , 2002, Inflammation Research.

[11]  R. Nosál',et al.  Cationic amphiphilic drugs and platelet phospholipase A(2) (cPLA(2)). , 2002, Thrombosis research.

[12]  M. Číž,et al.  Reactive Oxygen Metabolite Production is Inhibited by Histamine and H 1 -antagonist Dithiaden in Human PMN Leukocytes , 2002, Free radical research.

[13]  M. Church H1‐antihistamines and inflammation , 2001, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.