Gerrard J M, White J G, Rao G H, Townsend D
Am J Pathol. 1976 May;83(2):283-98.
Platelet production of 12L-hydroxy-5,8,10-heptadecatrienoic acid (HHT) and 8-(1-hydroxy-3-oxopropyl)-9, 12L-dihydroxy-5,10-heptadecadienoic acid (PHD), two metabolites of the prostaglandin cyclic endoperoxides PGG2 and PGH2, was found in this investigation to occur primarily in a platelet microsomal fraction consisting almost exclusively of membranes. To further localize the membrane site of platelet prostaglandin biosynthesis, the present study has used a cytochemical technique employing 3,3'-diaminobenzidine as an oxidizable substrate. The reaction product was found to localize in the platelet dense tubular system. Formation of the reaction product was inhibited by aminotriazole. In similar concentrations, aminotriazole inhibited collagen and arachidonic acid aggregation, the second wave of ADP and epinephrine aggregation, but failed to inhibit aggregation by PGG2 and A23187. A study of the mechanism of action of aminotriazole revealed inhibition of formation of HHT and PHD. The results localize platelet prostaglandin biosynthesis to the membranes of the dense tubular system.
在本研究中发现,血小板生成12L-羟基-5,8,10-十七碳三烯酸(HHT)和8-(1-羟基-3-氧代丙基)-9,12L-二羟基-5,10-十七碳二烯酸(PHD),这两种前列腺素环内过氧化物PGG2和PGH2的代谢产物,主要发生在几乎完全由膜组成的血小板微粒体部分。为了进一步定位血小板前列腺素生物合成的膜位点,本研究采用了一种细胞化学技术,使用3,3'-二氨基联苯胺作为可氧化底物。发现反应产物定位于血小板致密管状系统。氨基三唑抑制反应产物的形成。在相似浓度下,氨基三唑抑制胶原和花生四烯酸聚集、ADP和肾上腺素聚集的第二波,但未能抑制PGG2和A23187诱导的聚集。对氨基三唑作用机制的研究表明其抑制HHT和PHD的形成。结果将血小板前列腺素生物合成定位到致密管状系统的膜上。