Abdel-Latif A A, Smith J P
Biochim Biophys Acta. 1982 Jun 11;711(3):478-89. doi: 10.1016/0005-2760(82)90062-5.
The effects of the anti-inflammatory drugs, indomethacin and aspirin, and the phospholipase A2 inhibitors, p-bromophenacyl bromide and mepacrine, on the in vitro metabolism of [1-14C]arachidonic acid by rabbit iris smooth muscle and iris microsomes were investigated. The incorporation of arachidonate into glycerolipids and its conversion into prostaglandins were rapid and time-dependent. About 65% of the total radioactivity was recovered in triacylglycerol, followed by that in phosphatidylcholine (20%), diacylglycerol (6%), phosphatidylethanolamine (5%) and phosphatidylinositol (3%), respectively. Time-course studies on arachidonate release from glycerolipids of prelabelled tissue showed that triacylglycerol, phosphatidylcholine, phosphatidylethanolamine and phosphatidylinositol are the major source for arachidonate in prostaglandin synthesis in this tissue. Arachidonate release from glycerolipids was not blocked by indomethacin and the effects of the phospholipase A2 inhibitors were nonspecific. p-Bromophenacyl bromide inhibited the labelling of glycerolipids in a dose-dependent manner. Mepacrine stimulated the labelling of phosphatidic acid, phosphatidylinositol and diacylglycerol, and inhibited that of phosphatidylcholine, phosphatidylethanolamine and triacylglycerol. At concentrations under 0.25 mM it stimulated prostaglandin synthesis in microsomes and at concentrations over 0.25 mM it inhibited their synthesis in both muscle and microsomes. Indomethacin and aspirin moderately increased the labelling of glycerolipids; however, both drugs inhibited prostaglandin synthesis by iris and iris microsomes in a dose-dependent manner. Possible explanations for mechanisms underlying these effects were presented. It is concluded that the phospholipase A2 inhibitors and the anti-inflammatory drugs exert profound effects on the incorporation of [1-14C]arachidonate into glycerolipids of the rabbit iris and on its conversion into prostaglandins by both iris and iris microsomes.
研究了消炎药物吲哚美辛和阿司匹林,以及磷脂酶A2抑制剂对溴苯酰溴和米帕林,对兔虹膜平滑肌和虹膜微粒体中[1-14C]花生四烯酸体外代谢的影响。花生四烯酸掺入甘油脂质及其转化为前列腺素的过程迅速且具有时间依赖性。总放射性的约65%在三酰甘油中回收,其次分别在磷脂酰胆碱(20%)、二酰甘油(6%)、磷脂酰乙醇胺(5%)和磷脂酰肌醇(3%)中回收。对预先标记组织的甘油脂质中花生四烯酸释放的时间进程研究表明,三酰甘油、磷脂酰胆碱、磷脂酰乙醇胺和磷脂酰肌醇是该组织中前列腺素合成中花生四烯酸的主要来源。吲哚美辛未阻断甘油脂质中花生四烯酸的释放,磷脂酶A2抑制剂的作用是非特异性的。对溴苯酰溴以剂量依赖性方式抑制甘油脂质的标记。米帕林刺激磷脂酸、磷脂酰肌醇和二酰甘油的标记,并抑制磷脂酰胆碱、磷脂酰乙醇胺和三酰甘油的标记。在浓度低于0.25 mM时,它刺激微粒体中前列腺素的合成,在浓度高于0.25 mM时,它抑制肌肉和微粒体中前列腺素的合成。吲哚美辛和阿司匹林适度增加甘油脂质的标记;然而,两种药物均以剂量依赖性方式抑制虹膜和虹膜微粒体中前列腺素的合成。提出了这些作用潜在机制的可能解释。结论是,磷脂酶A2抑制剂和消炎药物对兔虹膜中[1-14C]花生四烯酸掺入甘油脂质以及虹膜和虹膜微粒体将其转化为前列腺素具有深远影响。