Inhibitory Effect of Nilvadipine on Disruption of Blood-Aqueous Barrier Induced by Prostaglandin E2 Application in Pigmented Rabbits: A Morphologic Study
| Autor: | Shigeyoshi Hiraki, Osamu Ohtani, Chiharu Kadoi, Seiji Hayasaka |
|---|---|
| Rok vydání: | 1999 |
| Předmět: |
Tight junction
biology Chemistry medicine.drug_class General Medicine Anatomy Calcium channel blocker Pharmacology Nilvadipine Horseradish peroxidase Sensory Systems Cellular and Molecular Neuroscience Ophthalmology medicine.anatomical_structure Cornea Blood-Aqueous Barrier medicine biology.protein Distribution (pharmacology) Prostaglandin E2 medicine.drug |
| Zdroj: | Ophthalmic Research. 31:236-242 |
| ISSN: | 1423-0259 0030-3747 |
| DOI: | 10.1159/000055538 |
| Popis: | The purpose of the present study is to investigate the morphologic sites of breakdown in eyes pretreated with nilvadipine (a calcium channel blocker) that has been shown to inhibit the acute rise of aqueous flare induced by prostaglandin E2 (PGE2). Nilvadipine (100 µg/kg body weight) was injected intravenously in pigmented rabbits. Thirty minutes later, vehicle or PGE2 (10, 50 or 250 µg/ml) was applied on the cornea by use of a glass cylinder. Forty-five minutes later, the animals received horseradish peroxidase (HRP) intravenously and the eyes were enucleated. Distribution of HRP in the anterior segments was observed by electron microscopy. Without nilvadipine pretreatment, HRP was seen in the intercellular space of nonpigmented cells of the eyes treated with 50 µg/ml PGE2 and in the iris stroma of the eyes treated with 250 µg/ml PGE2. With nilvadipine pretreatment, HRP was not observed in these sites. Our results indicate that nilvadipine suppresses disruption of the different sites of the blood-aqueous barrier. |
| Databáze: | OpenAIRE |
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