Flower R
Adv Prostaglandin Thromboxane Res. 1978;3:105-12.
It would seem that steroidal antiinflammatory drugs can block the prostaglandin endoperoxide releasing activity of a wide variety of stimuli. This seems to be due to an inhibition of the release of the fatty acid substrate since the effect is easily reversed by the addition of substrate. The effect of steroids on phospholipase A2 activity in lungs was investigated and it was found that these drugs inhibited the enzyme activity in a time-dependent reversible fashion and that they will block the effect of stimuli such as RCS-RF (bradykinin being an exception). The steroids do not appear to inhibit the phospholipase directly since they do not work in cell-free homogenates. It is too early to say whether or not the antiinflammatory activity of steroids depends on the actions. Many important experiments remain to be done, for example: what exactly is the nature of the phospholipase activation process? Which particular step are the steroids inhibiting? Why do they not work against bradykinin induced stimulation? We hope that in the not too distant future we shall be able to supply the answers to some of these questions.
甾体抗炎药似乎能够阻断多种刺激物的前列腺素内过氧化物释放活性。这似乎是由于对脂肪酸底物释放的抑制,因为添加底物后该效应很容易逆转。研究了甾体对肺中磷脂酶A2活性的影响,发现这些药物以时间依赖性可逆方式抑制该酶活性,并且它们会阻断诸如RCS-RF等刺激物的作用(缓激肽除外)。甾体似乎并不直接抑制磷脂酶,因为它们在无细胞匀浆中不起作用。现在说甾体的抗炎活性是否取决于这些作用还为时过早。还有许多重要的实验有待进行,例如:磷脂酶激活过程的确切性质是什么?甾体抑制的是哪个特定步骤?它们为何对缓激肽诱导的刺激不起作用?我们希望在不久的将来能够提供其中一些问题的答案。