Dual effect of isoprostanes on the release of [3H]D-aspartate from isolated bovine retinae: role of arachidonic acid metabolites.
Dual effect of isoprostanes on the release of [3H]D-aspartate from isolated bovine retinae: role of arachidonic acid metabolites.
复制标题
异前列烷对离体牛视网膜释放 [3H]D-天冬氨酸的双重作用:花生四烯酸代谢物的作用。
DOI:
10.1007/s11064-004-9694-3
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发表时间:
2005
影响因子:
4.4
通讯作者:
Ohia,SunnyE
中科院分区:
文献类型:
--
作者:
Opere,CatherineA;Zheng,WeiDong;Huang,Jifan;Adewale,Adeniran;Kruglet,Michael;Ohia,SunnyE
The effect of 8-isoprostanes on potassium (K+)-depolarization-evoked release of [3H]D-aspartate from bovine isolated retinae was investigated. Isolated bovine retinae were prepared for studies of K+-evoked release of [3H]D-aspartate using the Superfusion Method. Low concentrations of 8-isoPGF2α(1–100 nM) inhibited whereas higher concentrations of this 8-isoprostane (100 nM–30 μM) enhanced K+-induced [3H]D-aspartate overflow. The excitatory effect of 8-isoPGF2αwas mimicked by thromboxane receptor agonist, U-46619 and blocked by thromboxane receptor antagonist, SQ 29,548 (10 μM). Pretreatment of tissues with the cyclooxygenase (COX) inhibitor, flurbiprofen unmasked an inhibitory effect of high concentrations of 8-isoPGF2α(1–30 μM) on [3H]D-aspartate release that was attenuated by AH 6809 (10 μM). In conclusion, 8-isoPGF2αexhibits a dual regulatory effect on K+-induced [3H]D-aspartate release in isolated bovine retinae. The inhibitory action caused by 8-isoPGF2αis due to the activation of EP1/EP2receptors while the excitatory effects are due to the activation of thromboxane receptors.