de Bravo M M, De Tomás M E, Mercuri O
Biochem Int. 1985 Jun;10(6):889-96.
The microsomal fraction was used to test the ability of human platelets to metabolize gammalinolenic acid. The microsomal delta 6 and delta 5 fatty acid desaturase activities were measured and the incorporation of [14C]malonyl CoA into prostaglandins was also determined. The results indicate that human platelets have the capacity to elongate gammalinolenic acid (18:3 n-6) to dihomogammalinolenic acid (20:3 n-6) precursor of PGE1. Labeled PGE1 could be detected when human platelets microsomes were incubated with [14C]malonyl CoA in the presence of gammalinolenic acid. The results also show that human platelet microsomes have little delta 6 or delta 5 desaturase enzyme activity.
微粒体部分用于测试人血小板代谢γ-亚麻酸的能力。测定了微粒体δ6和δ5脂肪酸去饱和酶活性,并确定了[14C]丙二酰辅酶A掺入前列腺素的情况。结果表明,人血小板有能力将γ-亚麻酸(18:3 n-6)延长为PGE1的前体二高γ-亚麻酸(20:3 n-6)。当人血小板微粒体在γ-亚麻酸存在下与[14C]丙二酰辅酶A一起孵育时,可以检测到标记的PGE1。结果还表明,人血小板微粒体几乎没有δ6或δ5去饱和酶活性。