首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Vasodilator and constrictor actions of platelet-activating factor in the isolated microperfused afferent arteriole of the rabbit kidney. Role of endothelium-derived relaxing factoritric oxide and cyclooxygenase products.
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Vasodilator and constrictor actions of platelet-activating factor in the isolated microperfused afferent arteriole of the rabbit kidney. Role of endothelium-derived relaxing factoritric oxide and cyclooxygenase products.

机译:血小板活化因子在兔肾脏微灌流小动脉中的血管舒张和收缩作用。内皮源性松弛因子/一氧化氮和环氧合酶产物的作用。

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摘要

It has been suggested that platelet-activating factor (PAF) plays a prominent role in the control of glomerular hemodynamics in various physiological and pathological conditions. We examined the direct effect of PAF on rabbit glomerular afferent arterioles (Af-Arts) microperfused in vitro and tested whether endothelium-derived relaxing factoritric oxide (EDNO) and cyclooxygenase products are involved in its actions. In nanomolar concentrations PAF caused dose-dependent constriction of Af-Arts, with the maximum constriction being 34 +/- 10% at 4 x 10(-8) M (n = 9, P < 0.001). The constriction was blunted by cyclooxygenase inhibition (11 +/- 6%, n = 7, P < 0.05) but augmented by EDNO inhibition (76 +/- 14%, n = 8, P < 0.005). To study a possible vasodilator effect of PAF, Af-Arts were preconstricted with norepinephrine and increasing concentrations of PAF added to the lumen. At picomolar concentrations (lower than those that caused constriction), PAF produced dose-dependent vasodilation that was unaffected by cyclooxygenase inhibition but was abolished by EDNO synthesis inhibition. Both PAF-induced constriction and dilation of Af-Arts were blocked by a PAF receptor antagonist. This study demonstrates that PAF has a receptor-mediated biphasic effect on rabbit Af-Arts, dilating them at low concentrations while constricting them at higher concentrations. Our results suggest that PAF's vasodilator action may be due to production of EDNO, while its constrictor action is mediated at least in part through cyclooxygenase products.
机译:已经提出血小板活化因子(PAF)在各种生理和病理条件下在控制肾小球血流动力学中起着重要作用。我们检查了PAF对体外微灌流的兔肾小球传入小动脉(Af-Arts)的直接作用,并测试了内皮源性舒张因子/一氧化氮(EDNO)和环氧合酶产物是否参与其作用。在纳摩尔浓度下,PAF引起Af-Arts的剂量依赖性收缩,在4 x 10(-8)M时最大收缩为34 +/- 10%(n = 9,P <0.001)。通过环加氧酶抑制(11 +/- 6%,n = 7,P <0.05)使收缩收缩,但通过EDNO抑制(76 +/- 14%,n = 8,P <0.005)收缩。为了研究PAF可能的血管舒张作用,将Af-Arts与去甲肾上腺素预收缩,并在管腔中增加PAF的浓度。在皮摩尔浓度下(低于引起收缩的浓度),PAF产生剂量依赖性的血管舒张作用,该作用不受环氧合酶抑制的影响,但被EDNO合成抑制作用消除。 PAF受体拮抗剂可阻止PAF诱导的Af-Arts收缩和扩张。这项研究表明,PAF对兔Af-Arts具有受体介导的双相作用,在低浓度时会扩张,而在高浓度时会收缩。我们的结果表明,PAF的血管舒张作用可能是由于EDNO的产生,而其收缩作用至少部分是通过环氧合酶产物介导的。

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