Reynaud D, Pace-Asciak C R
Research Institute, Hospital for Sick Children, Toronto, Canada.
Biochim Biophys Acta. 1997 Jun 23;1346(3):305-16. doi: 10.1016/s0005-2760(97)00041-6.
Hepoxilins (Hx) are biologically active metabolites of arachidonic acid (AA) formed regioselectively from 12(S)-HPETE by 'hepoxilin synthase'. Hx modulate synaptic neurotransmission in hippocampal CA1 neurons, and inhibit norepinephrine release in hippocampal slices. During the course of our studies we investigated whether docosahexaenoic acid (DHA) was a substrate for hepoxilin formation. We used two tissues, the pineal gland and hippocampal slices. Tissues were incubated alone or with AA (20 microg/ml) or DHA (20 microg/ml). After 60 min at 37 degrees C, samples were acid-extracted to convert Hx into their stable trioxilin (TrX) form and analyzed as the Me-TMSi derivatives by EI-GC/MS to determine the structures of the DHA metabolites, and as PFB-TMSi derivatives by GC/MS in the NICI mode using SIM to simultaneously quantify TrX products of the 3-series (derived from AA) monitored at m/z 569, while those of the 5-series (derived from DHA) were monitored at m/z 593. Results show good conversion of both substrate fatty acids by the rat pineal gland and hippocampal slices, into the 3-series (21.3 +/- 5.8 and 12.5 +/- 2.2 ng/microg protein, respectively) and 5-series TrX (12.3 +/- 2.7 and 2.9 +/- 0.4 ng/microg protein, respectively). Surprisingly though, experiments with DHA, in both tissues, also showed formation of TrX derived from endogenous AA (3-series) (10.4 +/- 8.3 and 3.1 +/- 2.1 ng/microg protein, respectively). These experiments demonstrate previously unreported actions of DHA causing the accumulation of AA, which is converted into hepoxilins. In order to prove that AA is accumulated during DHA stimulation of the tissue, we carried out separate experiments with hippocampal slices in which the neutral lipids and phospholipids were labeled with [14C]AA. DHA caused a time-dependent appearance of free [14C]AA which was released mostly from the TG pool. Measurement of the AA/DHA ratio in the TG pool by GC/MS further indicated that DHA is incorporated into the TG at the expense of AA. These results demonstrate that DHA competes with AA for acylation into the metabolically active TG fraction, and both fatty acids are converted into hepoxilins of the corresponding series.
肝氧前列素(Hx)是花生四烯酸(AA)的生物活性代谢产物,由“肝氧前列素合酶”从12(S)-氢过氧化二十碳四烯酸(HPETE)区域选择性地生成。Hx调节海马CA1神经元的突触神经传递,并抑制海马切片中去甲肾上腺素的释放。在我们的研究过程中,我们研究了二十二碳六烯酸(DHA)是否是肝氧前列素形成的底物。我们使用了两种组织,松果体和海马切片。组织单独孵育或与AA(20微克/毫升)或DHA(20微克/毫升)一起孵育。在37℃孵育60分钟后,将样品进行酸提取,将Hx转化为其稳定的三氧前列素(TrX)形式,并通过EI-GC/MS分析为Me-TMSi衍生物以确定DHA代谢产物的结构,以及通过GC/MS在NICI模式下使用SIM分析为PFB-TMSi衍生物,以同时定量在m/z 569监测的3系列(源自AA)的TrX产物,而在m/z 593监测5系列(源自DHA)的TrX产物。结果表明,大鼠松果体和海马切片都能将两种底物脂肪酸良好地转化为3系列(分别为21.3±5.8和12.5±2.2纳克/微克蛋白质)和5系列TrX(分别为12.3±2.7和2.9±0.4纳克/微克蛋白质)。然而,令人惊讶的是,在两种组织中用DHA进行的实验还显示形成了源自内源性AA(3系列)的TrX(分别为10.4±8.3和3.1±2.1纳克/微克蛋白质)。这些实验证明了DHA以前未报道的作用,即导致AA积累,而AA会转化为肝氧前列素。为了证明在DHA刺激组织期间AA会积累,我们用海马切片进行了单独的实验,其中中性脂质和磷脂用[14C]AA标记。DHA导致游离[14C]AA呈时间依赖性出现,其主要从甘油三酯(TG)池中释放。通过GC/MS测量TG池中的AA/DHA比值进一步表明,DHA以AA为代价被掺入TG中。这些结果表明,DHA与AA竞争酰化进入代谢活性TG部分,并且两种脂肪酸都转化为相应系列的肝氧前列素。