Abstract | PURPOSE: METHODS: AMG, at 0.81, 81 or 81×10(3) μM, was instilled into the lower conjunctival fornix of normal and compound 48/80 (C48/80)-challenged eyes of male Wistar rats in the absence or presence of 40 mg/mL disodium cromoglycate. Histamine and nitrite were quantified in the conjunctival homogenate and lavage fluid 45 min and 6 h postchallenge, respectively. RESULTS: AMG induced no significant alterations in basal histamine and nitrite levels in the normal rat eye. In experimental conjunctivitis, AMG failed to modify the reduction in histamine content and partially circumvented the increases in nitrite levels observed during the early and late phase reactions, respectively. In the presence of disodium cromoglycate, AMG significantly increased the levels of both proinflammatory mediators in the normal rat eye. CONCLUSIONS: The data suggested that DAO may not be the main route of in situ histamine catabolism in the normal and C48/80-challenged rat conjunctiva, whereas NOS contributes to the phenotypic alterations observed in mast cell-dependent conjunctivitis. Mast cell stabilizing agents and AMG-modulated systems seem to interact through yet undefined mechanisms in the different phases of ocular hypersensitivity reactions.
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Authors | Miltiadis Papathanassiou, Vasiliki Giannoulaki, Evangelia Zampeli, Ekaterini Tiligada |
Journal | Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics
(J Ocul Pharmacol Ther)
Vol. 27
Issue 2
Pg. 137-42
(Apr 2011)
ISSN: 1557-7732 [Electronic] United States |
PMID | 21500983
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Guanidines
- Nitrites
- p-Methoxy-N-methylphenethylamine
- Histamine
- Nitric Oxide Synthase
- Amine Oxidase (Copper-Containing)
- Cromolyn Sodium
- pimagedine
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Topics |
- Amine Oxidase (Copper-Containing)
(antagonists & inhibitors, physiology)
- Animals
- Conjunctiva
(metabolism)
- Conjunctivitis
(etiology, metabolism)
- Cromolyn Sodium
(pharmacology)
- Guanidines
(pharmacology)
- Histamine
(analysis, metabolism)
- Male
- Mast Cells
(drug effects)
- Nitric Oxide Synthase
(antagonists & inhibitors, physiology)
- Nitrites
(analysis)
- Rats
- Rats, Wistar
- p-Methoxy-N-methylphenethylamine
(pharmacology)
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