Schimmel R J
Department of Physiology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, School of Osteopathic Medicine, Piscataway, 08854.
Biochem J. 1988 Jul 1;253(1):93-102. doi: 10.1042/bj2530093.
Previous studies of brown adipocytes identified an increased breakdown of phosphoinositides after selective alpha 1-adrenergic-receptor activation. The present paper reports that this response, elicited with phenylephrine in the presence of propranolol and measured as the accumulation of [3H]inositol phosphates, is accompanied by increased release of [3H]arachidonic acid from cells prelabelled with [3H]arachidonic acid. Differences between stimulated arachidonic acid release and formation of inositol phosphates included a requirement for extracellular Ca2+ for stimulated release of arachidonic acid but not for the formation of inositol phosphates and the preferential inhibition of inositol phosphate formation by phorbol 12-myristate 13-acetate. The release of arachidonic acid in response to phenylephrine was associated with an accumulation of [3H]arachidonic acid-labelled diacylglycerol, and this response was not dependent on extracellular Ca2+ but was partially prevented by treatment with the phorbol ester. The release of arachidonic acid was also stimulated by melittin, which increases the activity of phospholipase A2, by ionophore A23187, by lipolytic stimulation with forskolin and by exogenous phospholipase C. The arachidonic acid response to phospholipase C was completely blocked by RHC 80267, an inhibitor of diacylglycerol lipase, but this inhibitor had no effect on release stimulated with melittin or A23187 and inhibited phenylephrine-stimulated release by only 40%. The arachidonate response to forskolin was additive with the responses to either phenylephrine or exogenous phospholipase C. These data indicate that brown adipocytes are capable of releasing arachidonic acid from neutral lipids via triacylglycerol lipolysis, and from phospholipids via phospholipase A2 or by the sequential activities of phospholipase C and diacylglycerol lipase. Our findings also suggest that the action of phenylephrine to promote the liberation of arachidonic acid utilizes both of these reactions.
以往对棕色脂肪细胞的研究发现,选择性α1 -肾上腺素能受体激活后,磷酸肌醇的分解增加。本文报道,在普萘洛尔存在的情况下用去氧肾上腺素引发的这种反应,以[3H]肌醇磷酸的积累来衡量,伴随着预先用[3H]花生四烯酸标记的细胞中[3H]花生四烯酸释放的增加。刺激的花生四烯酸释放与肌醇磷酸形成之间的差异包括:刺激花生四烯酸释放需要细胞外Ca2+,而肌醇磷酸形成则不需要;佛波醇12 -肉豆蔻酸酯13 -乙酸盐对肌醇磷酸形成有优先抑制作用。对去氧肾上腺素的反应中,花生四烯酸的释放与[3H]花生四烯酸标记的二酰基甘油的积累相关,并且这种反应不依赖于细胞外Ca2+,但用佛波醇酯处理可部分阻止该反应。蜂毒素也能刺激花生四烯酸的释放,它可增加磷脂酶A2的活性,离子载体A23187、福斯高林的脂解刺激以及外源性磷脂酶C也有此作用。对磷脂酶C的花生四烯酸反应被二酰基甘油脂肪酶抑制剂RHC 80267完全阻断,但该抑制剂对蜂毒素或A23187刺激的释放没有影响,对去氧肾上腺素刺激的释放仅抑制40%。福斯高林引发的花生四烯酸反应与对去氧肾上腺素或外源性磷脂酶C的反应具有加和性。这些数据表明,棕色脂肪细胞能够通过三酰基甘油脂解从中性脂质中释放花生四烯酸,也能通过磷脂酶A2或磷脂酶C和二酰基甘油脂肪酶的顺序作用从磷脂中释放花生四烯酸。我们的研究结果还表明,去氧肾上腺素促进花生四烯酸释放的作用利用了这两种反应。