Farese R V, Kuo J Y, Babischkin J S, Davis J S
J Biol Chem. 1986 Jul 5;261(19):8589-92.
Insulin is known to increase the de novo synthesis of inositol phospholipids in rat epididymal fat pads. We presently examined the effects of insulin on the hydrolysis of inositol phospholipids in this tissue. Relatively small (30-40%) but significant increases in inositol phosphates (mono-, di-, and tri-) were apparent within 30-60 s of insulin treatment in fat pads (and adipocytes); thereafter, inositol phosphates returned to control levels. These rapid insulin-induced increases in inositol phosphates appeared to be due to phospholipase C-mediated hydrolysis of inositol phospholipids, since there were associated transient decreases in these lipids during 32P pulse-chase experiments. Increases in the synthesis of inositol phospholipids were also apparent within a few minutes of insulin treatment and persisted for at least 2 h. We conclude that, in the rat epididymal fat pad, insulin has two phospholipid effects, viz. a transient activation of phospholipase C, and a persistent increase in de novo phospholipid synthesis.
已知胰岛素可增加大鼠附睾脂肪垫中肌醇磷脂的从头合成。我们目前研究了胰岛素对该组织中肌醇磷脂水解的影响。在脂肪垫(和脂肪细胞)中,胰岛素处理30 - 60秒内,肌醇磷酸(单磷酸、二磷酸和三磷酸)相对小幅(30 - 40%)但显著增加;此后,肌醇磷酸恢复到对照水平。胰岛素诱导的这些肌醇磷酸的快速增加似乎是由于磷脂酶C介导的肌醇磷脂水解,因为在32P脉冲追踪实验期间这些脂质有相关的短暂减少。胰岛素处理几分钟内肌醇磷脂合成的增加也很明显,并持续至少2小时。我们得出结论,在大鼠附睾脂肪垫中,胰岛素对磷脂有两种作用,即磷脂酶C的短暂激活和磷脂从头合成的持续增加。