Russo-Marie F, Duval D
Biochim Biophys Acta. 1982 Jul 20;712(1):177-85. doi: 10.1016/0005-2760(82)90100-x.
Investigations were carried out to define the mechanisms of steroid-induced inhibition of prostaglandin secretion by rat renomedullary cells in tissue culture. Although it was strongly proposed that glucocorticoids may inhibit phospholipase A2 activity, we present several pieces of evidence against a direct action of dexamethasone on phospholipase activities. First, dexamethasone, which significantly decreases the release of labeled material from cells prelabeled with [3H]arachidonate, does not significantly alter the pattern of distribution of the radioactivity among the various classes of cell lipids. In addition, direct measurement of phospholipase A3 activity in dexamethasone-treated cells failed to show any significant decrease in the deacylation capacity. On the other hand, several indications suggest that dexamethasone may induce the secretion of a non-dialysable, transferable factor able to inhibit prostaglandin production, the mechanism of which remains to be investigated.
开展了多项研究以确定在组织培养中类固醇诱导大鼠肾髓质细胞前列腺素分泌受抑制的机制。尽管有强烈观点认为糖皮质激素可能抑制磷脂酶A2活性,但我们提供了几条证据反驳地塞米松对磷脂酶活性的直接作用。首先,地塞米松能显著降低用[3H]花生四烯酸预标记的细胞中标记物质的释放,但并未显著改变放射性在各类细胞脂质中的分布模式。此外,直接测量地塞米松处理细胞中的磷脂酶A3活性,未显示脱酰基能力有任何显著降低。另一方面,有若干迹象表明,地塞米松可能诱导分泌一种不可透析、可转移的因子,该因子能够抑制前列腺素的产生,其机制仍有待研究。