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α1-肾上腺素能受体介导的缺血大鼠心脏中磷脂酸和1,2-二酰甘油质量增加。

Alpha 1-adrenergic receptor-mediated increase in the mass of phosphatidic acid and 1,2-diacylglycerol in ischemic rat heart.

作者信息

Kurz T, Schneider I, Tölg R, Richardt G

机构信息

Medizinische Klinik II, Medizinische Universität zu Lübeck, Germany.

出版信息

Cardiovasc Res. 1999 Apr;42(1):48-56. doi: 10.1016/s0008-6363(98)00298-3.

Abstract

OBJECTIVE

1,2-Diacylglycerol (1,2-DAG) and phosphatidic acid (PA) are produced by phospholipase C and D activity and play a key role as second messengers in receptor-mediated signal transduction. So far, little is known about alterations of endogenous 1,2-DAG and PA production during myocardial ischemia.

METHODS

Rat isolated perfused hearts were subjected to global ischemia, total lipids were extracted, and separated by thin-layer chromatography. The mass of PA and 1,2-DAG were quantified using laserdensitometric analysis of visualized lipids.

RESULTS

Compared to normoxic control values (1,2-DAG 713 +/- 45 ng/mg protein, PA 171 +/- 11 ng/mg protein), the myocardial content of 1,2-DAG and PA was unaltered after 10 min of ischemia. Prolonged myocardial ischemia (20 min), however, which was accompanied by marked overflow of endogenous norepinephrine, significantly increased the mass of both second messengers (1,2-DAG 1062 +/- 100 ng/mg protein, PA 340 +/- 29 ng/mg protein). The increase in PA and 1,2-DAG in response to ischemia was abolished by inhibition of ischemia-induced norepinephrine release as well as by alpha1-adrenergic blockade but unaffected by beta-adrenergic blockade. While inhibition of diacylglycerol kinase did not affect ischemia-induced increase in PA and 1,2-DAG, inhibition of phosphatidylinositol-specific phospholipase C activity significantly suppressed ischemia-induced increase in 1,2-DAG but did not affect endogenous production of PA indicating phospholipase C-independent formation of PA and activation of both, phospholipase C and D, in the ischemic heart.

CONCLUSIONS

Ischemia elicits an alpha1-adrenergic receptor-mediated increase in the mass of myocardial PA and 1,2-DAG. The increase in endogenous PA is suggested to be due to the activation of myocardial phospholipase D, whereas 1,2-DAG is formed predominantly by activation of phospholipase C in the ischemic heart.

摘要

目的

1,2 - 二酰甘油(1,2 - DAG)和磷脂酸(PA)由磷脂酶C和D的活性产生,作为第二信使在受体介导的信号转导中起关键作用。到目前为止,关于心肌缺血期间内源性1,2 - DAG和PA产生的变化知之甚少。

方法

对大鼠离体灌注心脏进行全心缺血处理,提取总脂质,并用薄层色谱法分离。使用可视化脂质的激光密度分析法定量PA和1,2 - DAG的质量。

结果

与常氧对照值(1,2 - DAG 713±45 ng/mg蛋白质,PA 171±11 ng/mg蛋白质)相比,缺血10分钟后心肌中1,2 - DAG和PA的含量未发生改变。然而,长时间心肌缺血(20分钟),伴随着内源性去甲肾上腺素的明显溢出,显著增加了这两种第二信使的质量(1,2 - DAG 1062±100 ng/mg蛋白质,PA 34o±29 ng/mg蛋白质)。抑制缺血诱导的去甲肾上腺素释放以及α1 - 肾上腺素能阻断可消除缺血引起的PA和1,2 - DAG增加,但不受β - 肾上腺素能阻断的影响。虽然抑制二酰甘油激酶不影响缺血诱导的PA和1,2 - DAG增加,但抑制磷脂酰肌醇特异性磷脂酶C活性可显著抑制缺血诱导的1,2 - DAG增加,但不影响PA的内源性产生,表明PA的形成不依赖磷脂酶C,且缺血心脏中磷脂酶C和D均被激活。

结论

缺血引发α1 - 肾上腺素能受体介导的心肌PA和1,2 - DAG质量增加。内源性PA的增加被认为是由于心肌磷脂酶D的激活,而1,2 - DAG主要是由缺血心脏中磷脂酶C的激活形成的。

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