Preud'homme Y, Demolle D, Boeynaems J M
Invest Ophthalmol Vis Sci. 1985 Oct;26(10):1336-42.
Both the iris and the retina of the rabbit released prostaglandins (PG) E2, F2 alpha, 6-keto-F1 alpha and thromboxane (Tx) B2, when incubated in vitro. PGE2 was the major cyclooxygenase product formed by each tissue. The kinetics of PGE2 release by the iris and the retina were similar: high initial output followed by a decline to a steady-state value. The production of PGE2 was inhibited by indomethacin and stimulated by ionophore A23187. The iris and the retina converted exogenous arachidonic acid into 12- and 15-hydroxy-eicosatetraenoic acid (HETE): inhibition by eicosatetraynoic acid (ETYA) indicated the involvement of lipoxygenase enzymes. This lipoxygenase activity was important relatively to cyclooxygenase in the retina, but was only a minor pathway in the iris. Leukotriene (LT) B4 was released by the iris and the retina in amounts smaller than PGE2, but compatible with a biological activity: ionophore A23187 stimulated LTB4 production in both tissues. Our data support the hypothesis that PGE2 and LTB4 could play a role in the initiation of ocular inflammation.
家兔的虹膜和视网膜在体外孵育时均释放前列腺素(PG)E2、F2α、6-酮-F1α和血栓素(Tx)B2。PGE2是每个组织形成的主要环氧化酶产物。虹膜和视网膜释放PGE2的动力学相似:初始输出量高,随后下降至稳态值。吲哚美辛抑制PGE2的产生,离子载体A23187刺激其产生。虹膜和视网膜将外源性花生四烯酸转化为12-和15-羟基二十碳四烯酸(HETE):二十碳四炔酸(ETYA)的抑制作用表明脂氧合酶参与其中。这种脂氧合酶活性在视网膜中相对于环氧化酶较为重要,但在虹膜中只是一条次要途径。虹膜和视网膜释放的白三烯(LT)B4量比PGE2少,但具有生物活性:离子载体A23187刺激两种组织中LTB4的产生。我们的数据支持以下假设,即PGE2和LTB4可能在眼部炎症的起始中起作用。