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前列腺素作为炎症介质。

Prostaglandins as mediators of inflammation.

作者信息

Vane J R

出版信息

Adv Prostaglandin Thromboxane Res. 1976;2:791-801.

PMID:790919
Abstract
  1. Nonsteroid antiinflammatory drugs inhibit prostaglandin biosynthesis in concentrations likely to be found in body fluids during therapy. The assembled evidence, together with the actions of prostaglandins, overwhelmingly supports the theory that this antienzyme effect is the mechanism of action of aspirin-like drugs. 2. Intermediates in prostaglandin biosynthesis and their nonprostaglandin derivatives such as RCS (thromboxane A2) may also play a part in the inflammatory process. 3. There is a close interplay between bradykinin and prostaglandins, not only in inflammation, but also in other systems. 4. Bradykinin stimulates phospholipase A2, thereby making available prostaglandin precursors.
摘要
  1. 非甾体抗炎药在治疗期间体液中可能存在的浓度下抑制前列腺素生物合成。综合证据以及前列腺素的作用,有力地支持了这种抗酶作用是阿司匹林类药物作用机制的理论。2. 前列腺素生物合成中的中间体及其非前列腺素衍生物,如RCS(血栓素A2),也可能在炎症过程中起作用。3. 缓激肽与前列腺素之间存在密切的相互作用,不仅在炎症中如此,在其他系统中也是如此。4. 缓激肽刺激磷脂酶A2,从而使前列腺素前体得以利用。

相似文献

1
Prostaglandins as mediators of inflammation.前列腺素作为炎症介质。
Adv Prostaglandin Thromboxane Res. 1976;2:791-801.
2
[The roll of prostaglandins and catecholamines in inflammation and in the mode of action of antiphlogistics].
Pharmazie. 1974 Oct-Nov;29(10-11):671-80.
3
Evolution of ideas on the role of prostaglandins in inflammation.关于前列腺素在炎症中作用的观点演变
Agents Actions Suppl. 1980;7:247-51.
4
The effects of prostagladin endoperoxides and thromboxane A2 on strips of rabbit coeliac artery and certain other smooth muscle preparations [proceedings].前列腺素内过氧化物和血栓素A2对兔腹腔动脉条及某些其他平滑肌制剂的作用[会议论文集]
Br J Pharmacol. 1976 Jul;57(3):462P-463P.
5
Mechanisms underlying inflammatory edema: the importance of synergism between prostaglandins, leukotrienes, and complement-derived peptides.炎症性水肿的潜在机制:前列腺素、白三烯和补体衍生肽之间协同作用的重要性。
Adv Prostaglandin Thromboxane Leukot Res. 1983;11:33-7.
6
[The prostaglandin-thromboxan system].[前列腺素-血栓素系统]
Schweiz Med Wochenschr. 1977 Jun 4;107(22):753-6.
7
Bradykinin-induced contraction is inhibited by tiaramide, an anti-inflammatory drug, with an inhibition of increase in intracellular free calcium.缓激肽诱导的收缩受到抗炎药物替拉米特的抑制,同时细胞内游离钙的增加也受到抑制。
J Pharmacol Exp Ther. 1988 Aug;246(2):635-40.
8
Antiinflammatory drugs and the many mediators of inflammation.
Int J Tissue React. 1987;9(1):1-14.
9
Proceedings: Formation of prostaglandin endoperoxides and rabbit aorta contracting substance (RCS) by coupling two enzyme systems.论文:通过偶联两个酶系统形成前列腺素内过氧化物和兔主动脉收缩物质(RCS)。
Br J Pharmacol. 1976 Mar;56(3):344P-345P.
10
Relationship between prostaglandins and lysophosphatides in the inflammatory process.
Agents Actions Suppl. 1979(4):286-92.

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