H1-antihistamines and oxidative burst of professional phagocytes

Neuro Endocrinol Lett. 2009:30 Suppl 1:133-6.

Abstract

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.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzothiepins / pharmacology
  • Brompheniramine / pharmacology
  • Chlorpheniramine / pharmacology
  • Dose-Response Relationship, Drug
  • Extracellular Space / drug effects
  • Histamine H1 Antagonists / administration & dosage
  • Histamine H1 Antagonists / pharmacology*
  • Humans
  • Intracellular Space / drug effects
  • Loratadine / pharmacology
  • Luminescence
  • Luminol / analogs & derivatives
  • Neutrophils / drug effects*
  • Neutrophils / metabolism
  • Oxidation-Reduction / drug effects
  • Pheniramine / pharmacology
  • Respiratory Burst / drug effects*

Substances

  • Benzothiepins
  • Histamine H1 Antagonists
  • Pheniramine
  • isoluminol
  • Chlorpheniramine
  • dithiadene
  • Luminol
  • Loratadine
  • Brompheniramine