Participation of Histamine H3 Receptors in Experimental Allergic Rhinitis of Mice
doi: 10.1254/jphs.08164fp
pmid: 18845911
Participation of Histamine H3 Receptors in Experimental Allergic Rhinitis of Mice
The present study was performed to study the participation of histamine H(3) receptors in nasal symptoms using Sch 50971, a potent and selective agonist of the H(3) receptor. Repeated topical application of antigen caused an increase in sneezing and nasal rubbing in sensitized mice. Oral administration of Sch 50971 and imetit, specific H(3)-receptor agonists, resulted in an inhibition of nasal symptoms induced by an antigen similar to an H(1)-receptor antagonist, cetirizine. Furthermore, simultaneous use of H(3)-receptor agonists, Sch 50971 or imetit, and an H(1)-receptor antagonist, cetirizine, caused a significant inhibitory effect on nasal symptoms at doses that showed no effect when used separately. The number of eosinophils in the nasal mucosa of mice sensitized with antigen was significantly decreased by cetirizine; however, Sch 50971 and imetit had no effect on eosinophil infiltration. These results clearly indicate that H(3) receptors are involved in the etiology of nasal allergy, and the stimulation of H(3) receptors may be useful as a novel therapeutic approach in nasal allergy.
- Okayama University Japan
Histamine H1 Antagonists, Non-Sedating, Pyrrolidines, Rhinitis, Allergic, Perennial, Ovalbumin, RM1-950, Histamine Agonists, Mice, Anti-Allergic Agents, Animals, Receptors, Histamine H3, Mice, Inbred BALB C, Dose-Response Relationship, Drug, Pruritus, Imidazoles, Drug Synergism, Cetirizine, Eosinophils, Chemotaxis, Leukocyte, Disease Models, Animal, Nasal Mucosa, Female, Therapeutics. Pharmacology
Histamine H1 Antagonists, Non-Sedating, Pyrrolidines, Rhinitis, Allergic, Perennial, Ovalbumin, RM1-950, Histamine Agonists, Mice, Anti-Allergic Agents, Animals, Receptors, Histamine H3, Mice, Inbred BALB C, Dose-Response Relationship, Drug, Pruritus, Imidazoles, Drug Synergism, Cetirizine, Eosinophils, Chemotaxis, Leukocyte, Disease Models, Animal, Nasal Mucosa, Female, Therapeutics. Pharmacology
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