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1
Endothelium-derived relaxing factor alters calcium fluxes in rabbit aorta: a cyclic guanosine monophosphate-mediated effect.内皮源性舒张因子改变兔主动脉中的钙通量:一种环磷酸鸟苷介导的效应。
J Physiol. 1986 Dec;381:427-37. doi: 10.1113/jphysiol.1986.sp016336.
2
Endothelium-derived relaxing factor and nitroprusside compared in noradrenaline- and K+-contracted rabbit and rat aortae.在去甲肾上腺素和钾离子收缩的兔和大鼠主动脉中比较内皮衍生舒张因子和硝普钠。
J Physiol. 1988 Jun;400:395-404. doi: 10.1113/jphysiol.1988.sp017127.
3
Endothelium-derived relaxing factor inhibits the formation of inositol trisphosphate by rabbit aorta.内皮衍生舒张因子抑制兔主动脉中肌醇三磷酸的形成。
J Physiol. 1989 Apr;411:45-52. doi: 10.1113/jphysiol.1989.sp017558.
4
Effects of metabolic inhibitors on endothelium-dependent and endothelium-independent vasodilatation of rat and rabbit aorta.代谢抑制剂对大鼠和兔主动脉内皮依赖性及非内皮依赖性血管舒张的影响。
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5
Release of endothelium-derived relaxing factor is inhibited by 8-bromo-cyclic guanosine monophosphate.内皮源性舒张因子的释放受到8-溴环磷酸鸟苷的抑制。
J Cardiovasc Pharmacol. 1988 Dec;12(6):672-7. doi: 10.1097/00005344-198812000-00008.
6
Vascular smooth muscle sensitivity to endothelium-derived relaxing factor is different in different arteries.血管平滑肌对内皮源性舒张因子的敏感性在不同动脉中有所不同。
Br J Pharmacol. 1988 Oct;95(2):630-6. doi: 10.1111/j.1476-5381.1988.tb11685.x.
7
Effect of endothelium on basal and on stimulated accumulation and efflux of cyclic GMP in rat isolated aorta.内皮对大鼠离体主动脉中环鸟苷酸基础水平及刺激后积累与流出的影响。
Br J Pharmacol. 1989 Jul;97(3):853-65. doi: 10.1111/j.1476-5381.1989.tb12025.x.
8
Differences in basal endothelium-derived relaxing factor activity in different artery types.不同动脉类型中基础内皮衍生舒张因子活性的差异。
J Cardiovasc Pharmacol. 1986 Nov-Dec;8(6):1158-62. doi: 10.1097/00005344-198611000-00010.
9
LY 83583 (6-anilino-5,8-quinolinedione) blocks nitrovasodilator-induced cyclic GMP increases and inhibition of platelet activation.LY 83583(6-苯胺基-5,8-喹啉二酮)可阻断硝基血管扩张剂诱导的环磷酸鸟苷增加以及对血小板活化的抑制作用。
Naunyn Schmiedebergs Arch Pharmacol. 1989 Jul;340(1):119-25. doi: 10.1007/BF00169217.
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Sodium nitroprusside alters Ca2+ flux components and Ca2(+)-dependent fluxes of K+ and Cl- in rat aorta.硝普钠改变大鼠主动脉中的Ca2+通量成分以及K+和Cl-的Ca2(+)-依赖性通量。
J Physiol. 1990 Feb;421:411-24. doi: 10.1113/jphysiol.1990.sp017952.

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The relationship between lymphangion chain length and maximum pressure generation established through in vivo imaging and computational modeling.通过体内成像和计算建模建立的淋巴管链长度与最大压力产生之间的关系。
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The endothelium and its role in regulating vascular tone.内皮及其在调节血管张力中的作用。
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Voltage-gated calcium channel currents in human coronary myocytes. Regulation by cyclic GMP and nitric oxide.人类冠状动脉心肌细胞中的电压门控钙通道电流。环磷酸鸟苷和一氧化氮的调节作用。
J Clin Invest. 1997 Jan 15;99(2):185-93. doi: 10.1172/JCI119146.
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Endothelium-dependent and NO-mediated desensitization to vasopressin in rat aorta.大鼠主动脉中内皮依赖性及一氧化氮介导的对血管加压素的脱敏作用。
Br J Pharmacol. 1996 Nov;119(5):899-904. doi: 10.1111/j.1476-5381.1996.tb15757.x.
7
Endothelium, for example.例如,内皮。
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8
Effects of 8-bromoguanosine 3':5'-cyclic monophosphate on phenylephrine-induced phosphatidylinositol hydrolysis and contraction in rat caudal artery.8-溴鸟苷3':5'-环一磷酸对去氧肾上腺素诱导的大鼠尾动脉磷脂酰肌醇水解和收缩的影响。
Br J Pharmacol. 1995 Sep;116(1):1697-703. doi: 10.1111/j.1476-5381.1995.tb16394.x.
9
A comparison of the inhibitory effects of sodium nitroprusside, pinacidil and nifedipine on pressor response to NG-nitro-L-arginine.硝普钠、吡那地尔和硝苯地平对NG-硝基-L-精氨酸升压反应的抑制作用比较。
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10
Maxi K+ channels are stimulated by cyclic guanosine monophosphate-dependent protein kinase in canine coronary artery smooth muscle cells.在犬冠状动脉平滑肌细胞中,大电导钾通道受环磷酸鸟苷依赖性蛋白激酶刺激。
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本文引用的文献

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The regeneration of aortic endothelium.主动脉内皮的再生。
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2
Cellular basis of nitroprusside-induced relaxation of graded responses to norepinephrine and potassium in canine renal arteries.硝普钠诱导犬肾动脉对去甲肾上腺素和钾的分级反应舒张的细胞基础。
Arch Int Pharmacodyn Ther. 1980 Jun;245(2):198-210.
3
A comparative study of the relaxing effect of nitroprusside and verapamil on human umbilical vessels.硝普钠与维拉帕米对人脐血管舒张作用的比较研究。
Blood Vessels. 1981;18(6):321-9. doi: 10.1159/000158365.
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Effects of sodium gradient manipulation upon cellular calcium, 45Ca fluxes and cellular sodium in the guinea-pig taenia coli.钠梯度调控对豚鼠结肠带细胞钙、45Ca通量及细胞钠的影响
J Physiol. 1981;319:443-61. doi: 10.1113/jphysiol.1981.sp013920.
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Mechanism of activation of isolated rabbit aorta by PGH2 analogue U-44069.PGH2类似物U-44069对离体兔主动脉的激活机制。
Am J Physiol. 1981 Nov;241(5):C243-9. doi: 10.1152/ajpcell.1981.241.5.C243.
6
Isolated perfused rabbit coronary artery and aortic strip preparations: the role of endothelium-derived relaxant factor.离体灌注兔冠状动脉和主动脉条制备:内皮源性舒张因子的作用
J Physiol. 1984 Jun;351:13-24. doi: 10.1113/jphysiol.1984.sp015228.
7
The nature of endothelium-derived vascular relaxant factor.内皮源性血管舒张因子的本质。
Nature. 1984;308(5960):645-7. doi: 10.1038/308645a0.
8
Mechanisms of the nitroglycerine-induced vasodilation in vascular smooth muscles of the rabbit and pig.硝酸甘油诱导兔和猪血管平滑肌血管舒张的机制。
J Physiol. 1983 Oct;343:233-52. doi: 10.1113/jphysiol.1983.sp014890.
9
Effects of cAMP- and cGMP-dependent protein kinases, and calmodulin on Ca2+ uptake by highly purified sarcolemmal vesicles of vascular smooth muscle.环磷酸腺苷(cAMP)依赖性蛋白激酶、环磷酸鸟苷(cGMP)依赖性蛋白激酶及钙调蛋白对血管平滑肌高度纯化肌膜囊泡摄取钙离子的影响
Biochim Biophys Acta. 1984 Jun 13;773(1):83-90. doi: 10.1016/0005-2736(84)90552-2.
10
Comparative effects of verapamil and sodium nitroprusside on contraction and 45Ca uptake in the smooth muscle of rabbit aorta, rat aorta and guinea-pig taenia coli.维拉帕米和硝普钠对兔主动脉、大鼠主动脉及豚鼠结肠带平滑肌收缩和45钙摄取的比较效应。
Br J Pharmacol. 1984 Feb;81(2):393-400. doi: 10.1111/j.1476-5381.1984.tb10091.x.

内皮源性舒张因子改变兔主动脉中的钙通量:一种环磷酸鸟苷介导的效应。

Endothelium-derived relaxing factor alters calcium fluxes in rabbit aorta: a cyclic guanosine monophosphate-mediated effect.

作者信息

Collins P, Griffith T M, Henderson A H, Lewis M J

出版信息

J Physiol. 1986 Dec;381:427-37. doi: 10.1113/jphysiol.1986.sp016336.

DOI:10.1113/jphysiol.1986.sp016336
PMID:3498027
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1182988/
Abstract
  1. Measurement of tension and 45Ca influx and efflux were used to study the effects of endothelium-derived relaxing factor (EDRF), sodium nitroprusside and 8-bromo-cyclic guanosine monophosphate (GMP) on contractile responses and calcium movements in aortic ring preparations of the rabbit. 2. EDRF activity, induced by stimulating endothelium-containing rings with acetylcholine, was associated with relaxation of noradrenaline-constricted rings and with a marked reduction of noradrenaline-stimulated increase in calcium influx. Sodium nitroprusside and 8-bromo-cyclic GMP had a similar effect in de-endothelialized preparations. 3. EDRF also inhibited noradrenaline-stimulated calcium efflux. Sodium nitroprusside and 8-bromo-cyclic GMP had a similar effect in de-endothelialized preparations, both in the presence and absence of extracellular calcium. 4. The vascular smooth muscle relaxant effect of EDRF and of nitrovasodilators may be effected by a cyclic GMP-mediated reduction of cytosolic calcium, through both inhibition of calcium influx and reduction of intracellular calcium release.
摘要
  1. 采用张力测定以及45钙内流和外流测定法,研究内皮源性舒张因子(EDRF)、硝普钠和8-溴环鸟苷单磷酸(GMP)对兔主动脉环标本收缩反应和钙转运的影响。2. 用乙酰胆碱刺激含内皮的血管环所诱导的EDRF活性,与去甲肾上腺素收缩的血管环舒张以及去甲肾上腺素刺激引起的钙内流增加的显著减少有关。硝普钠和8-溴环GMP在去内皮的标本中有类似作用。3. EDRF还抑制去甲肾上腺素刺激的钙外流。硝普钠和8-溴环GMP在去内皮的标本中,无论有无细胞外钙存在时均有类似作用。4. EDRF和硝基血管扩张剂的血管平滑肌舒张作用可能是通过环GMP介导的胞质钙减少来实现的,这是通过抑制钙内流和减少细胞内钙释放两种方式达成的。