Hidaka T, Wong P Y, Malik K U
Prostaglandins. 1980 May;19(5):805-18. doi: 10.1016/0090-6980(80)90176-8.
Infusion of [14C] arachidonic acid (AA) into the isolated, Tyrode perfused rabbit spleen resulted in the release of a substance into the venous effluent with the musculotropic activity and chromatographic properties of prostaglandin (PG)E2. Smaller amounts of radioactive materials with the chromatographic properties of PGF2 alpha, 6-keto-PGF1 alpha, and PGD2 were also released. The radiolabeled material released in largest amounts from the spleen was identified as PGE2 on the basis of: 1) Co-chromatography with PGE2 in three solvent systems, 2) Conversion of the radioactive material and of authentic [3H] PGE2 to similar products by treatment with sodium borohydride and with potassium hydroxide, and 3) Stability of the musculotropic activity in Tyrode solution at 37 degrees C. Release of the major and minor radioactive products was inhibited by pretreatment of the spleen with either indomethacin or 5,8,11,14-eicosatetraynoic acid.
将[14C]花生四烯酸(AA)注入离体的、用台氏液灌注的兔脾脏,导致一种具有前列腺素(PG)E2的肌促活性和色谱特性的物质释放到静脉流出液中。还释放出少量具有PGF2α、6-酮-PGF1α和PGD2色谱特性的放射性物质。基于以下几点,从脾脏中释放量最大的放射性标记物质被鉴定为PGE2:1)在三种溶剂系统中与PGE2共色谱;2)通过硼氢化钠和氢氧化钾处理,放射性物质和 authentic [3H] PGE2转化为相似产物;3)在37℃台氏液中肌促活性的稳定性。用吲哚美辛或5,8,11,14-二十碳四烯酸预处理脾脏可抑制主要和次要放射性产物的释放。