Abstract | AIMS: METHODS: RESULTS:
Retinal ischaemia/reperfusion caused cell loss in the ganglion cell layer and thinning of the inner plexiform and nuclear layer. Both ocular topical and intravenous administration of 2-CN-Ado caused a reduction of retinal ischaemia/ reperfusion damage. A selective A2A receptor antagonist, 1,3,7-trimethyl-8-(3-chlorostyryl) xanthine (CSC), but not a selective A1 receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine ( DPCPX), or a selective A2B receptor antagonist, alloxazine, reduced the protective effect of 2-CN-Ado. While ocular topical administration of 2-CN-Ado caused a sustained reduction of intraocular pressure, intravenous administration of 2-CN-Ado showed a transient ocular hypotensive effect. CONCLUSIONS:
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Authors | T Konno, A Sato, T Uchibori, A Nagai, K Kogi, N Nakahata |
Journal | The British journal of ophthalmology
(Br J Ophthalmol)
Vol. 90
Issue 7
Pg. 900-5
(Jul 2006)
ISSN: 0007-1161 [Print] England |
PMID | 16613921
(Publication Type: Journal Article)
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Chemical References |
- 2-(6-cyano-1-hexyn-1-yl)adenosine
- Adenosine A2 Receptor Agonists
- Antihypertensive Agents
- Excitatory Amino Acid Antagonists
- Phenethylamines
- 2-(4-(2-carboxyethyl)phenethylamino)-5'-N-ethylcarboxamidoadenosine
- Dizocilpine Maleate
- Adenosine
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Topics |
- Adenosine
(analogs & derivatives, chemistry, pharmacology, therapeutic use)
- Adenosine A2 Receptor Agonists
- Administration, Topical
- Animals
- Antihypertensive Agents
(pharmacology)
- Dizocilpine Maleate
(pharmacology)
- Excitatory Amino Acid Antagonists
(pharmacology)
- Intraocular Pressure
(drug effects)
- Ischemic Preconditioning
- Male
- Phenethylamines
(pharmacology)
- Rats
- Rats, Sprague-Dawley
- Reperfusion Injury
(metabolism, pathology, prevention & control)
- Retinal Vessels
(metabolism, pathology)
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