Kass M A, Holmberg N J
Invest Ophthalmol Vis Sci. 1979 Feb;18(2):166-71.
Microsomes of albino rabbit ocular tissues were incubated with (1-14C)-arachidonic acid for 15 min at 37 degrees C. Thin-layer chromatography revealed that ciliary body-iris microsomes were capable of synthesizing prostaglandin F2alpha (PGF2alpha), PGE2, PGD2, thromboxane B2(TXB2), and 6-keto-PGF1alpha. Indomethacin 14 micrometer in the incubation medium essentially abolished all prostaglandin synthesis detectable by this method. Imidazole 10 mM in the incubation medium inhibited only TXB2 synthesis. Ciliary body-iris microsomes were incubated for 2 min at 0 degrees C with PGH2. The products of this reaction were superfused over spiral strips of rabbit aorta and produced the strong contractions typical of TXA2. Addition to imidazole to the incubation medium blocked the formation of the contracting substance. Incubation of ciliary body-iris microsomes with (1-14C)--8,11,14-eicosatrienoic acid produced PGF1alpha, PGD1, and PGE1 but no evidence of any thromboxane product or 6-keto-PGF1alpha. Conjunctival and corneal microsomes synthesized prostaglandins, although less effectively than ciliary body-iris microsomes, when incubated with (1-14C)-arachidonic acid. Microsomes of sclera, retina-choroid, and lens synthesized little, if any, prostaglandins.
将白化兔眼组织的微粒体与(1-¹⁴C)-花生四烯酸在37℃下孵育15分钟。薄层色谱显示,睫状体-虹膜微粒体能够合成前列腺素F2α(PGF2α)、PGE2、PGD2、血栓素B2(TXB2)和6-酮-PGF1α。孵育培养基中14微摩尔的吲哚美辛基本上消除了用该方法可检测到的所有前列腺素合成。孵育培养基中10毫摩尔的咪唑仅抑制TXB2的合成。睫状体-虹膜微粒体在0℃下与PGH2孵育2分钟。该反应的产物灌注到兔主动脉螺旋条上,产生了典型的TXA2强烈收缩。向孵育培养基中添加咪唑可阻止收缩物质的形成。睫状体-虹膜微粒体与(1-¹⁴C)-8,11,14-二十碳三烯酸孵育产生PGF1α、PGD1和PGE1,但没有任何血栓素产物或6-酮-PGF1α的证据。结膜和角膜微粒体与(1-¹⁴C)-花生四烯酸孵育时,虽然合成前列腺素的效率低于睫状体-虹膜微粒体,但也能合成前列腺素。巩膜、视网膜-脉络膜和晶状体的微粒体几乎不合成前列腺素(如果有合成的话)。