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在用 NG-硝基-L-精氨酸甲酯阻断内皮舒张因子生物合成后,下腔静脉对去甲肾上腺素和乙酰胆碱的反应性改变。

Altered reactivity of the inferior vena cava to noradrenaline and acetylcholine following the blockade of EDRF-biosynthesis with NG-nitro-L-arginine methyl ester.

作者信息

Schwarzacher S, Krejcy K, Ferber W, Weidinger F

机构信息

Department of Cardiology, University of Vienna Medical School, Austria.

出版信息

Clin Exp Pharmacol Physiol. 1996 Jun-Jul;23(6-7):490-2. doi: 10.1111/j.1440-1681.1996.tb02766.x.

DOI:10.1111/j.1440-1681.1996.tb02766.x
PMID:8800571
Abstract
  1. Endothelium-derived relaxing factor (EDRF) has been shown to influence arterial tone, but controversial results have been obtained studying veins. The present study was performed to determine the importance of EDRF for the inferior vena cava in the rabbit and whether blockade of the synthesis of EDRF with NG-nitro-L-arginine methyl ester may influence the reactivity of the inferior vena cava to noradrenaline. 2. The inferior vena cava was excised in six New Zealand white rabbits and 12 rings were prepared for organ bath studies. Concentration-response curves were constructed for acetylcholine (10(-9)-10(-4) mol/L) and noradrenaline (10(-9)-10(-4) mol/L) before and following the administration of NG-nitro-L-arginine methyl ester. 3. All rings showed concentration-dependent relaxation to acetylcholine (mean maximum: 57 +/- 9%) following precontraction with noradrenaline (EC50:10(-6) mol/L). Following NG-nitro-L-arginine methyl ester, this dilation was significantly reduced to a mean maximum relaxation of 13 +/- 6% (P < 0.01). 4. Contraction of the inferior vena cava to increasing doses of noradrenaline reached a maximum of 5.8 +/- 2.8 g before NG-nitro-L-arginine methyl ester (basal tension 1.0 +/- 0.5 g). NG-nitro-L-arginine methyl ester did not affect basal tension, but the constrictor response to noradrenaline was enhanced significantly to a maximum of 9.1 +/- 3.8 g (P < 0.01). 5. Although it cannot be ascertained definitively from the present results, it is suggested that EDRF is mediating vasodilation of the inferior vena cava and that this vasoactive agent may also contributes significantly to the modulation of the reactivity to catecholamines.
摘要
  1. 内皮衍生舒张因子(EDRF)已被证明可影响动脉张力,但在研究静脉时却得到了相互矛盾的结果。本研究旨在确定EDRF对兔下腔静脉的重要性,以及用NG-硝基-L-精氨酸甲酯阻断EDRF的合成是否会影响下腔静脉对去甲肾上腺素的反应性。2. 取6只新西兰白兔的下腔静脉,制备12个环用于器官浴研究。在给予NG-硝基-L-精氨酸甲酯之前和之后,构建乙酰胆碱(10^(-9)-10^(-4)mol/L)和去甲肾上腺素(10^(-9)-10^(-4)mol/L)的浓度-反应曲线。3. 在用去甲肾上腺素预收缩后,所有环对乙酰胆碱均呈现浓度依赖性舒张(平均最大舒张:57±9%)(半数有效浓度:10^(-6)mol/L)。给予NG-硝基-L-精氨酸甲酯后,这种舒张显著降低至平均最大舒张13±6%(P<0.01)。4. 下腔静脉对递增剂量去甲肾上腺素的收缩在给予NG-硝基-L-精氨酸甲酯前达到最大值5.8±2.8g(基础张力1.0±0.5g)。NG-硝基-L-精氨酸甲酯不影响基础张力,但对去甲肾上腺素的收缩反应显著增强至最大值9.1±3.8g(P<0.01)。5. 尽管从目前的结果不能明确确定,但提示EDRF介导下腔静脉的血管舒张,并且这种血管活性物质可能也对儿茶酚胺反应性的调节有显著贡献。

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