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人单核细胞中前列腺素内过氧化物合酶-2的诱导与环氧化酶依赖性F2-异前列腺素的形成相关。

Induction of prostaglandin endoperoxide synthase-2 in human monocytes associated with cyclo-oxygenase-dependent F2-isoprostane formation.

作者信息

Patrignani P, Santini G, Panara M R, Sciulli M G, Greco A, Rotondo M T, di Giamberardino M, Maclouf J, Ciabattoni G, Patrono C

机构信息

Department of Pharmacology, University of Chieti G. D'Annunzio School of Medicine, Italy.

出版信息

Br J Pharmacol. 1996 Jul;118(5):1285-93. doi: 10.1111/j.1476-5381.1996.tb15535.x.

Abstract
  1. The isoprostane 8-epi-prostaglandin (PG)F2 alpha is produced by free radical-catalyzed peroxidation of arachidonic acid. It may also be formed as a minor product of the cyclo-oxygenase activity of platelet PGH synthase (PGHS)-1. We investigated 8-epi-PGF2 alpha production associated with induction of the human monocyte PGHS-2 and its pharmacological modulation. 2. Heparinized whole blood samples were drawn from healthy volunteers, 48 h following oral dosing with aspirin 300 mg to suppress platelet cyclo-oxygenase activity. One ml aliquots were incubated with lipopolysaccharide (LPS: 0.1-50 micrograms ml-1) for 0-24 h at 37 degrees C. PGE2 and 8-epi-PGF2 alpha were measured in separated plasma by radioimmunoassay and enzyme immunoassay techniques. 3. Levels of both eicosanoids were undetectable (i.e. < 60 pg ml-1) at time 0. LPS induced the formation of PGE2 and 8-epi-PGF2 alpha in a time- and concentration-dependent fashion, coincident with the induction of PGHS-2 detected by Western blot analysis of monocyte lysates. After 24 h at 10 micrograms ml-1 LPS, immunoreactive PGE2 and 8-epi-PGF2 alpha averaged 10,480 +/- 4,643 and 295 +/- 140 pg ml-1 (mean +/- s.d., n = 6), respectively. 4. Dexamethasone and 5-methanesulphonamido-6-(2,4-difluorothiophenyl)-1-indano ne (L-745,337), a selective inhibitor of the cyclo-oxygenase activity of PGHS-2, reduced PGE2 and 8-epi-PGF2 alpha production in response to LPS. 5. Isolated monocytes produced PGE2 and 8-epi-PGE2 alpha in response to LPS (10 micrograms ml-1) in a time-dependent fashion. Monocyte PGE2 and 8-epi-PGF2 alpha production was largely prevented by dexamethasone (2 microM) and cycloheximide (10 micrograms ml-1) in association with suppression of PGHS-2 but not of PGHS-1 expression. 6. We conclude that the induction of PGHS-2 in human monocytes is associated with cyclo-oxygenase-dependent generation of the vasoconstrictor and platelet-agonist 8-epi-PGF2 alpha.
摘要
  1. 异前列腺素8-表-前列腺素(PG)F2α由花生四烯酸的自由基催化过氧化反应产生。它也可能作为血小板PGH合酶(PGHS)-1环氧化酶活性的次要产物形成。我们研究了与人类单核细胞PGHS-2诱导相关的8-表-PGF2α产生及其药理调节作用。2. 在给健康志愿者口服300 mg阿司匹林以抑制血小板环氧化酶活性48小时后,采集肝素化全血样本。将1 ml等分试样与脂多糖(LPS:0.1 - 50 μg/ml)在37℃孵育0 - 24小时。通过放射免疫分析和酶免疫分析技术在分离的血浆中测量PGE2和8-表-PGF2α。3. 在时间0时,两种类花生酸的水平均检测不到(即<60 pg/ml)。LPS以时间和浓度依赖性方式诱导PGE2和8-表-PGF2α的形成,这与通过单核细胞裂解物的蛋白质印迹分析检测到的PGHS-2诱导一致。在10 μg/ml LPS作用24小时后,免疫反应性PGE2和8-表-PGF2α的平均值分别为10480±4643和295±140 pg/ml(平均值±标准差,n = 6)。4. 地塞米松和5-甲磺酰胺基-6-(2,4-二氟噻吩基)-1-茚酮(L-745,337),一种PGHS-2环氧化酶活性的选择性抑制剂,可降低对LPS反应时PGE2和8-表-PGF2α的产生。5. 分离的单核细胞对LPS(10 μg/ml)以时间依赖性方式产生PGE2和8-表-PGE2α。地塞米松(2 μM)和环己酰亚胺(10 μg/ml)在抑制PGHS-2而非PGHS-1表达的同时,很大程度上阻止了单核细胞PGE2和8-表-PGF2α的产生。6. 我们得出结论,人类单核细胞中PGHS-2的诱导与血管收缩剂和血小板激动剂8-表-PGF2α的环氧化酶依赖性生成有关。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f77/1909586/a35e2d6091e1/brjpharm00084-0211-a.jpg

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