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9α,11β-前列腺素F2,一种前列腺素D2的新型代谢产物,是人和豚鼠气道的强效收缩激动剂。

9 alpha,11 beta-prostaglandin F2, a novel metabolite of prostaglandin D2 is a potent contractile agonist of human and guinea pig airways.

作者信息

Beasley C R, Robinson C, Featherstone R L, Varley J G, Hardy C C, Church M K, Holgate S T

出版信息

J Clin Invest. 1987 Mar;79(3):978-83. doi: 10.1172/JCI112909.

Abstract

Prostaglandin (PG) D2, the predominant prostanoid released from activated mast cells in humans is initially metabolized by reduction of the C-11 keto function to yield 9 alpha,11 beta-PGF2. In this study the airways effects of 9 alpha,11 beta-PGF2 were compared with those of its epimer 9 alpha,11 alpha-PGF2 (PGF2 alpha) and PGD2. 9 alpha,11 beta-PGF2 was a potent contractile agonist of isolated guinea pig trachea and 4-mm human airways in vitro; the potencies of the PGs relative to PGD2 (= 1.00) being 0.65 (NS) and 4.08 (P less than 0.001) for 9 alpha,11 beta-PGF2, and 0.52 (P less than 0.01) and 2.40 (P less than 0.001) for PGF2 alpha, respectively. When inhaled by asthmatic subjects, 9 alpha,11 beta-PGF2 was a potent bronchoconstrictor agent, being approximately equipotent with PGD2 and 28-32 times more potent than histamine (P less than 0.01). These studies suggest that 9 alpha,11 beta-PGF2 is at least equipotent with PGD2 as a bronchoconstrictor agonist, and in being a major metabolite of PGD2, could contribute to the bronchoconstrictor effect of this mast cell-derived mediator in asthma.

摘要

前列腺素(PG)D2是人类活化肥大细胞释放的主要前列腺素类物质,最初通过C-11酮功能的还原进行代谢,生成9α,11β-PGF2。在本研究中,比较了9α,11β-PGF2与其差向异构体9α,11α-PGF2(PGF2α)和PGD2对气道的影响。9α,11β-PGF2是离体豚鼠气管和4毫米人气道的强效收缩激动剂;相对于PGD2(=1.00),9α,11β-PGF2的效力分别为0.65(无显著性差异)和4.08(P<0.001),PGF2α的效力分别为0.52(P<0.01)和2.40(P<0.001)。哮喘患者吸入9α,11β-PGF2后,它是一种强效支气管收缩剂,效力与PGD2大致相当,比组胺强28 - 32倍(P<0.01)。这些研究表明,9α,11β-PGF2作为支气管收缩激动剂至少与PGD2效力相当,并且作为PGD2的主要代谢产物,可能在哮喘中促成这种肥大细胞衍生介质的支气管收缩作用。

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