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首页> 外文期刊>The Journal of Experimental Biology >The heart of Ciona intestinalis: eicosanoid-generating capacity and the effects of precursor fatty acids and eicosanoids on heart rate
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The heart of Ciona intestinalis: eicosanoid-generating capacity and the effects of precursor fatty acids and eicosanoids on heart rate

机译:Ciona intestinalis的心脏:类花生酸的产生能力以及前体脂肪酸和类花生酸对心率的影响

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Eicosanoids are a group of oxygenated fatty-acid derivatives formed from C20 polyunsaturated fatty acids including arachidonic and eicosapentaenoic acids. In mammals, these compounds have been shown to be key molecules in several physiological processes including regulation of the vascular system. This study determined whether eicosanoids or their precursors are involved in the regulation of heart rate in the sea squirt Ciona intestinalis. Eicosanoid generation by both heart and blood cells was measured. The major lipoxygenase products formed were both derivatives of eicosapentaenoic acid, namely 8- and 12-hydroxyeicosapentaenoic acids (8-HEPE and 12-HEPE). Smaller amounts of 8,15-dihydroxyeicosapentaenoic acid (8,15-diHEPE) were also formed. The cyclo-oxygenase product prostaglandin E was also found in small amounts in the heart. Isolated hearts were exposed either to these fatty acid precursors or to 8-HEPE, 12-HEPE or prostaglandin E-3, and the effect on heart rate was recorded. Both eicosapentaenoic and arachidonic acids stimulated the heart rate at concentrations between 50 and 200 mumol l(-1). 12-HEPE (5 mumol l(-1)) and prostaglandin E-3 (50 mumol l(-1)) caused a modest increase in heart rate, while 8-REPE had no significant effects at any of the time periods studied (less than or equal to180 min). Overall, the results show that arachidonic and eicosapentaenoic acids have limited effects on heart rate and only at concentrations unlikely to be routinely liberated in vivo. Similarly, the eicosanoids tested had a minor stimulatory activity on heart rate. The potential mechanisms for this stimulation are discussed. Overall, these results suggest that such compounds are of limited importance in regulating the heart and vascular system of sea squirts. [References: 35]
机译:类二十烷酸是由包括花生四烯酸和二十碳五烯酸的C20多不饱和脂肪酸形成的一组含氧脂肪酸衍生物。在哺乳动物中,这些化合物已被证明是包括调节血管系统在内的几种生理过程中的关键分子。这项研究确定了类花生酸或它们的前体是否参与了海鞘Ciona intestinalis的心率调节。测量了心脏和血细胞中类花生酸的生成。形成的主要脂氧合酶产物都是二十碳五烯酸的衍生物,即8和12-羟基二十碳五烯酸(8-HEPE和12-HEPE)。还形成了少量的8,15-二羟基二十碳五烯酸(8,15-diHEPE)。心脏中也发现了少量的环氧合酶产物前列腺素E。离体的心脏暴露于这些脂肪酸前体或8-HEPE,12-HEPE或前列腺素E-3,并记录了对心率的影响。二十碳五烯酸和花生四烯酸都可以在50至200μmoll(-1)的浓度下刺激心率。 12-HEPE(5μmoll(-1))和前列腺素E-3(50μmoll(-1))引起心率适度增加,而8-REPE在所研究的任何时间段均无明显影响(小于或等于180分钟)。总体而言,结果表明,花生四烯酸和二十碳五烯酸对心率的影响有限,并且仅在不太可能在体内常规释放的浓度下起作用。同样,所测试的类二十烷酸对心率的刺激作用较小。讨论了这种刺激的潜在机制。总体而言,这些结果表明,此类化合物在调节海鞘的心脏和血管系统方面具有有限的重要性。 [参考:35]

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