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激肽与抗炎类固醇。

Kinins and anti-inflammatory steroids.

作者信息

Eisen V, Greenbaum L, Lewis G P

出版信息

Br J Pharmacol. 1968 Sep;34(1):169-76. doi: 10.1111/j.1476-5381.1968.tb07960.x.

Abstract
  1. This investigation was designed to re-examine the possibility that anti-inflammatory steroids interfere with the kinin-forming system.2. We conclude that the anti-inflammatory action of corticosteroids cannot be explained by the inhibition of kinin formation. This view is based on the following findings.3. Neither hydrocortisone nor prednisolone nor dexamethasone inhibited the activation or activity of intrinsic plasma kinin forming enzymes resulting from dilution, incubation with kininase inhibitors, or exposure to glass, monosodium urate microcrystals or to precipitated complexes of rheumatoid factor and aggregated human gamma-globulin.4. Hydrocortisone did not inhibit the action of the active kinin-forming enzymes, human salivary or urinary kallikrein, or plasmin on purified kininogen.5. Hydrocortisone, prednisolone and dexamethasone did not inhibit the hydrolysis of benzoyl-arginine-ethyl ester by human plasmin, plasma kallikrein or hog pancreatic kallikrein.6. Kinin formation occurred normally in plasma taken from two patients receiving betamethasone and one receiving prednisone.
摘要
  1. 本研究旨在重新审视抗炎类固醇干扰激肽形成系统的可能性。

  2. 我们得出结论,皮质类固醇的抗炎作用不能用抑制激肽形成来解释。这一观点基于以下发现。

  3. 氢化可的松、泼尼松龙或地塞米松均未抑制因稀释、与激肽酶抑制剂孵育或暴露于玻璃、尿酸钠微晶或类风湿因子与聚集的人γ球蛋白沉淀复合物而导致的内源性血浆激肽形成酶的激活或活性。

  4. 氢化可的松不抑制活性激肽形成酶、人唾液或尿激肽释放酶或纤溶酶对纯化激肽原的作用。

  5. 氢化可的松、泼尼松龙和地塞米松不抑制人纤溶酶、血浆激肽释放酶或猪胰激肽释放酶对苯甲酰精氨酸乙酯的水解。

  6. 从两名接受倍他米松治疗的患者和一名接受泼尼松治疗的患者采集的血浆中,激肽形成正常发生。

相似文献

1
Kinins and anti-inflammatory steroids.激肽与抗炎类固醇。
Br J Pharmacol. 1968 Sep;34(1):169-76. doi: 10.1111/j.1476-5381.1968.tb07960.x.

本文引用的文献

4
Analgesic-antipyretic drugs as inhibitors of kallikrein.作为激肽释放酶抑制剂的解热镇痛药
Br J Pharmacol Chemother. 1961 Aug;17(1):107-15. doi: 10.1111/j.1476-5381.1961.tb01110.x.
5
The purification of a kininogen from human plasma.从人血浆中纯化一种激肽原。
Br J Pharmacol Chemother. 1966 Aug;27(2):256-76. doi: 10.1111/j.1476-5381.1966.tb01661.x.
6

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