Westfall T C, Carpentier S, Chen X, Beinfeld M C, Naes L, Meldrum M J
Department of Pharmacology, St. Louis University School of Medicine, Missouri 63104.
J Cardiovasc Pharmacol. 1987 Dec;10(6):716-22. doi: 10.1097/00005344-198712000-00016.
The effect of neuropeptide Y (NPY) on periarterial nerve stimulation-induced release of norepinephrine (NE) and increase in perfusion pressure in the perfused mesenteric arterial bed of the rat was examined. Perfusate effluents were continuously collected and assayed for endogenous NE by high-pressure liquid chromatography (HPLC) coupled to electrochemical detection. Perfusion pressure was continuously monitored by means of a pressure transducer. Periarterial nerve stimulation (8 or 16 Hz, 60 V, 2-ms duration for 30 s) resulted in a readily detectable increase in NE release and perfusion pressure that was attenuated by the prior administration of tetrodotoxin (TTX) (10(-5) M) or guanethidine (5 X 10(-5) M). NPY exerted both prejunctional and postjunctional effects on noradrenergic neurotransmission in this preparation. The peptide produced a concentration-dependent reduction in the release of NE over a concentration range of 10(-10) - 10(-7) M. A similar inhibition effect occurred at 8, 10, and 16 Hz. In contrast, low concentrations (10(-10) and 10(-9) M) decreased the effect of nerve stimulation on perfusion pressure, whereas higher concentrations (10(-7) M) produced a marked potentiation. The alpha 2-adrenoceptor antagonist, yohimbine, did not alter the inhibitory effect of NPY on evoked NE release or the effect on perfusion pressure. Prazosin similarly did not alter the inhibitory effect of NPY on NE release but prevented the increase in perfusion pressure. We conclude that NPY modulates noradrenergic neurotransmission in the mesenteric arterial bed by decreasing the evoked release of NE and producing a concentration-dependent biphasic response on vascular smooth muscle.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了神经肽Y(NPY)对大鼠肠系膜动脉床动脉周围神经刺激诱导的去甲肾上腺素(NE)释放及灌注压升高的影响。连续收集灌流液流出物,采用高压液相色谱(HPLC)结合电化学检测法测定内源性NE。通过压力传感器连续监测灌注压。动脉周围神经刺激(8或16Hz,60V,2ms持续时间,共30s)导致NE释放和灌注压明显升高,预先给予河豚毒素(TTX)(10⁻⁵M)或胍乙啶(5×10⁻⁵M)可减弱这种升高。在该制备中,NPY对去甲肾上腺素能神经传递发挥了节前和节后作用。该肽在10⁻¹⁰ - 10⁻⁷M浓度范围内使NE释放呈浓度依赖性减少。在8、10和16Hz时出现类似的抑制作用。相反,低浓度(10⁻¹⁰和10⁻⁹M)降低了神经刺激对灌注压的影响,而高浓度(10⁻⁷M)则产生明显增强作用。α₂肾上腺素能受体拮抗剂育亨宾未改变NPY对诱发的NE释放的抑制作用或对灌注压的影响。哌唑嗪同样未改变NPY对NE释放的抑制作用,但阻止了灌注压的升高。我们得出结论,NPY通过减少诱发的NE释放并对血管平滑肌产生浓度依赖性双相反应来调节肠系膜动脉床的去甲肾上腺素能神经传递。(摘要截断于250字)