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本文引用的文献

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Formation of monohydroxyeicosatetraenoic acids from arachidonic acid by cultured rabbit aortic smooth muscle cells.培养的兔主动脉平滑肌细胞将花生四烯酸转化为单羟基二十碳四烯酸
Biochem Biophys Res Commun. 1983 Apr 15;112(1):242-9. doi: 10.1016/0006-291x(83)91822-3.
2
The effects of BW755C and other anti-inflammatory drugs on eicosanoid concentrations and leukocyte accumulation in experimentally-induced acute inflammation.BW755C及其他抗炎药物对实验性诱导急性炎症中类花生酸浓度和白细胞聚集的影响。
J Pharm Pharmacol. 1983 Dec;35(12):808-13. doi: 10.1111/j.2042-7158.1983.tb02901.x.
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Formation of 15-HETE as a major hydroxyeicosatetraenoic acid in the atherosclerotic vessel wall.15-羟基二十碳四烯酸(15-HETE)作为动脉粥样硬化血管壁中主要的羟基二十碳四烯酸的形成。
Biochim Biophys Acta. 1985 Apr 25;834(2):272-4. doi: 10.1016/0005-2760(85)90166-3.
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Bovine and human endothelial cell production of neutrophil chemoattractant activity in response to components of the angiotensin system.牛和人内皮细胞对血管紧张素系统成分产生中性粒细胞趋化活性。
Circ Res. 1985 Dec;57(6):898-902. doi: 10.1161/01.res.57.6.898.
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Effects of leukotriene D4 on glomerular dynamics in the rat.白三烯D4对大鼠肾小球动力学的影响。
Am J Physiol. 1987 Aug;253(2 Pt 2):F239-43. doi: 10.1152/ajprenal.1987.253.2.F239.
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Histamine stimulation of prostaglandin and HETE synthesis in human endothelial cells.组胺对人内皮细胞中前列腺素和羟二十碳四烯酸合成的刺激作用。
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Mechanism of action of some inhibitors of endothelium-derived relaxing factor.一些内皮源性舒张因子抑制剂的作用机制。
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Endothelium-dependent contractions to acetylcholine in the aorta of the spontaneously hypertensive rat.自发性高血压大鼠主动脉中对乙酰胆碱的内皮依赖性收缩
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Age and hypertension promote endothelium-dependent contractions to acetylcholine in the aorta of the rat.年龄和高血压会促使大鼠主动脉对乙酰胆碱产生内皮依赖性收缩。
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10
Activation of endothelial L-arginine pathway in resistance arteries. Effect of age and hypertension.阻力动脉中内皮型L-精氨酸途径的激活。年龄和高血压的影响。
Hypertension. 1990 Aug;16(2):170-9. doi: 10.1161/01.hyp.16.2.170.

一氧化氮、花生四烯酸的环氧化酶和脂氧化酶产物在大鼠肾弓状动脉收缩反应中的相对作用。

Relative roles of nitric oxide and cyclo-oxygenase and lipoxygenase products of arachidonic acid in the contractile responses of rat renal arcuate arteries.

作者信息

Wu X C, Richards N T, Michael J, Johns E

机构信息

Department of Physiology, University of Birmingham, Edgbaston.

出版信息

Br J Pharmacol. 1994 Jun;112(2):369-76. doi: 10.1111/j.1476-5381.1994.tb13081.x.

DOI:10.1111/j.1476-5381.1994.tb13081.x
PMID:8075854
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1910375/
Abstract
  1. We have examined the effects of inhibition of nitric oxide synthase, cyclo-oxygenase and lipoxygenase on the responses of renal arcuate arteries of Wistar rats, with and without endothelium, to noradrenaline, potassium chloride, endothelin-1, acetylcholine and sodium nitroprusside. 2. Noradrenaline, potassium chloride and endothelin-1 caused concentration-dependent contraction of the vessels. Indomethacin (14 microM) attenuated the contractile response to noradrenaline and to potassium chloride. The inhibitory effect of indomethacin persisted following endothelial removal. 3. Acetylcholine produced concentration-dependent relaxation of the vessels which was potentiated by indomethacin (14 microM). 4. NG-nitro-L-arginine methyl ester (L-NAME, 100 microM) did not affect the contractile response to either noradrenaline or potassium chloride but abolished relaxation to acetylcholine. In addition, L-NAME abolished the affects of indomethacin on acetylcholine-induced relaxation and noradrenaline- and potassium chloride-induced contraction. 5. BWC755C attenuated noradrenaline and potassium chloride-induced contraction. This effect persisted in the presence of indomethacin. 6. In vessels pretreated with CHAPS, BW755C inhibited both noradrenaline and potassium chloride-induced contraction. In these vessels BW755C had no additional inhibitory effect to indomethacin on noradrenaline- and potassium-induced contraction. 7. Inhibition of nitric oxide synthase with L-NAME (100 microM) attenuated the effect of BW755C on noradrenaline- and potassium-induced contraction. 8. BW755C alone did not affect endothelium-dependent relaxation as assessed by the response to acetylcholine. However, in the presence of indomethacin, BW755C inhibited acetylcholine-induced relaxation. 9. BW755C did not affect endothelium-independent relaxation as assessed by the response to sodium nitroprusside in vessels with or without endothelium. 10. These data support the existence of two vasoconstrictor products of arachidonic acid released during contraction of renal arcuate arteries with noradrenaline and potassium chloride. A cyclooxygenase product which appears to be endothelium-independent and the other an endothelium dependent lipoxygenase product.
摘要
  1. 我们研究了一氧化氮合酶、环氧化酶和脂氧合酶的抑制作用对有内皮和无内皮的Wistar大鼠肾弓状动脉对去甲肾上腺素、氯化钾、内皮素 -1、乙酰胆碱和硝普钠反应的影响。2. 去甲肾上腺素、氯化钾和内皮素 -1引起血管浓度依赖性收缩。吲哚美辛(14微摩尔)减弱了对去甲肾上腺素和氯化钾的收缩反应。内皮去除后,吲哚美辛的抑制作用仍然存在。3. 乙酰胆碱引起血管浓度依赖性舒张,吲哚美辛(14微摩尔)可增强这种舒张作用。4. NG -硝基 -L -精氨酸甲酯(L - NAME,100微摩尔)不影响对去甲肾上腺素或氯化钾的收缩反应,但消除了对乙酰胆碱的舒张反应。此外,L - NAME消除了吲哚美辛对乙酰胆碱诱导舒张以及去甲肾上腺素和氯化钾诱导收缩的影响。5. BWC755C减弱了去甲肾上腺素和氯化钾诱导的收缩。在存在吲哚美辛的情况下,这种作用仍然存在。6. 在经CHAPS预处理的血管中,BW755C抑制去甲肾上腺素和氯化钾诱导的收缩。在这些血管中,BW755C对吲哚美辛对去甲肾上腺素和钾诱导收缩的抑制作用没有额外影响。7. 用L - NAME(100微摩尔)抑制一氧化氮合酶减弱了BW755C对去甲肾上腺素和钾诱导收缩的作用。8. 单独使用BW755C时,根据对乙酰胆碱的反应评估,其不影响内皮依赖性舒张。然而,在存在吲哚美辛的情况下,BW755C抑制乙酰胆碱诱导的舒张。9. 根据对硝普钠的反应评估,在有内皮和无内皮的血管中,BW755C均不影响非内皮依赖性舒张。10. 这些数据支持在肾弓状动脉与去甲肾上腺素和氯化钾收缩过程中释放的两种花生四烯酸血管收缩产物的存在。一种似乎是非内皮依赖性的环氧化酶产物,另一种是内皮依赖性的脂氧合酶产物。