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持续内毒素血症大鼠肝细胞中甘油二酯积累对血管加压素刺激反应的动力学

Kinetics of diacylglycerol accumulation in response to vasopressin stimulation in hepatocytes of continuously endotoxaemic rats.

作者信息

Rodriguez de Turco E B, Spitzer J A

机构信息

Department of Physiology, Louisiana State University Medical Center, New Orleans 70112.

出版信息

Biochem J. 1988 Jul 1;253(1):73-9. doi: 10.1042/bj2530073.

Abstract

The content and composition of 1,2-diacyl-sn-glycerol (1,2-DAG) was determined in hepatocytes from saline (0.9% NaCl)- and Escherichia coli endotoxin (ET)-infused rats upon continuous vasopressin (VP) (10(-8) M) stimulation. In both experimental groups the accumulation of 1,2-DAG was detected after a lag period (2-5 min), was sustained up to the last time analysed (10 min), and C18:0- and C20:4-fatty-acid-containing-DAG accumulation preceded that of DAG containing other acyl groups. In hepatocytes from ET-infused rats the VP-induced accumulation of DAG was delayed and was decreased by 50%, showing a C18:0/C20:4 molar ratio of 1.6 as compared with 1.1 for cells from saline-infused rats. A similar lower cellular response to VP stimulation was observed in cells prelabelled with [14C]C20:4 fatty acid. The accumulation of [14C]C20:4-DAG (lower in ET than in saline-infused rats) was paralleled by a decrease in phosphatidylinositol (PI) labelling, whereas phosphatidic acid showed a transient increase by 5 min in saline- but not in ET-infused rats. The present results demonstrate that the previously reported impairment in the early degradation of poly-PI and later in the 'PI cycle' during VP stimulation [Rodriguez de Turco & Spitzer (1987) Metab. Clin. Exp. 36, 753-760] is also reflected at the level of their phosphodiesteratic product, DAG. Moreover, the kinetics of the accumulation of DAG acyl groups is consistent with the idea that the initial release of C18:0- and C20:4-DAG (possibly derived from inositol lipids) could regulate the subsequent enlargement of this pool by stimulating a phospholipase C-mediated degradation of other phospholipids (e.g. phosphatidylcholine).

摘要

在持续给予血管加压素(VP,10⁻⁸ M)刺激的情况下,测定了生理盐水(0.9% NaCl)灌注和大肠杆菌内毒素(ET)灌注大鼠肝细胞中1,2 - 二酰基 - sn - 甘油(1,2 - DAG)的含量和组成。在两个实验组中,1,2 - DAG的积累在延迟期(2 - 5分钟)后被检测到,并持续到最后一次分析时间(10分钟),且含C18:0和C20:4脂肪酸的DAG积累先于含其他酰基的DAG。在ET灌注大鼠的肝细胞中,VP诱导的DAG积累延迟且减少了50%,与生理盐水灌注大鼠的细胞相比,其C18:0/C20:4摩尔比为1.6,而生理盐水灌注大鼠的细胞该比值为1.1。在用[¹⁴C]C20:4脂肪酸预标记的细胞中,也观察到对VP刺激的类似较低细胞反应。[¹⁴C]C20:4 - DAG的积累(ET灌注大鼠低于生理盐水灌注大鼠)与磷脂酰肌醇(PI)标记的减少平行,而在生理盐水灌注但非ET灌注大鼠中,磷脂酸在5分钟时显示出短暂增加。目前的结果表明,先前报道的在VP刺激期间多聚 - PI早期降解以及随后“PI循环”中的损伤[Rodriguez de Turco & Spitzer(1987年),《代谢、临床与实验》36,753 - 760]在其磷酸二酯产物DAG水平上也有所体现。此外,DAG酰基积累的动力学与以下观点一致,即C18:0和C20:4 - DAG(可能源自肌醇脂质)的初始释放可通过刺激磷脂酶C介导的其他磷脂(如磷脂酰胆碱)降解来调节该池随后的扩大。

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本文引用的文献

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