Inhibition of Potassium- and Ischemia-Evoked [3H] D-Aspartate Release from Isolated Bovine Retina by Cannabinoids

We investigated the effect of cannabinoids on potassium chloride (K+)- and ischemia-induced [3H]D-aspartate release from isolated bovine retinae. The superfusion method was employed for studies of [3H]-neurotransmitter release. Cannabinoid receptor CB1 agonists, but not the CB2 agonist JWH 015, inhi...

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Veröffentlicht in:Current eye research 2006-01, Vol.31 (7-8), p.645-653
Hauptverfasser: Opere, Catherine A., Zheng, Wei Dong, Zhao, Min, Lee, Jin Sook, Kulkarni, Kaustubh H., Ohia, Sunny E.
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Sprache:eng
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Zusammenfassung:We investigated the effect of cannabinoids on potassium chloride (K+)- and ischemia-induced [3H]D-aspartate release from isolated bovine retinae. The superfusion method was employed for studies of [3H]-neurotransmitter release. Cannabinoid receptor CB1 agonists, but not the CB2 agonist JWH 015, inhibited K+-induced [3H]D-aspartate release from bovine retinae with the following rank order of activity: anandamide > ACEA > methanandamide > WIN 55,212-2. In the ischemic model, the rank order of activity was as follows: methanandamide > ACEA > WIN 55,212-2. The CB1 receptor antagonist AM 251 blocked inhibitory responses produced by cannabinoids in both experimental conditions. In conclusion, cannabinoids inhibit evoked [3H]D-aspartate release from isolated bovine retinae via an effect on CB1 receptors.
ISSN:0271-3683
1460-2202
DOI:10.1080/02713680600762747