Moriarty M, Potter E K, McCloskey D I
Prince of Wales Medical Research Institute, Sydney, NSW, Australia.
J Auton Nerv Syst. 1993 Oct;45(1):21-8. doi: 10.1016/0165-1838(93)90358-2.
The effects of a long-lasting intravenous infusion of neuropeptide Y (NPY, 180 +/- 8 min, 53 +/- 4 micrograms/kg/h) on the prolonged inhibition of cardiac vagal action evoked by cardiac sympathetic nerve stimulation and bolus intravenous injections of NPY were investigated in anaesthetised dogs. Sympathetic stimulation and NPY injection were performed on four separate occasions; once in control conditions, then once early and again late in the period of NPY infusion, and then on a final occasion 60-90 min after the cessation of NPY infusion. The maximum inhibition of cardiac vagal action evoked by an injection of NPY was significantly less late in the NPY infusion when compared with the other three injection groups (ANOVA, P < 0.001). Also the time to half-recovery of this response was significantly less than that seen in the other three injection groups (ANOVA, P < 0.001). The maximum inhibition of cardiac vagal action evoked by sympathetic stimulation was significantly reduced late in the NPY infusion when compared with the other three stimulation groups (ANOVA, P < 0.0001). The time for half-recovery of this response was also less than that of the other three stimulation groups (ANOVA, P < 0.001). The results indicate that desensitisation of the vagal attenuation to both exogenous NPY and sympathetic stimulation occurred during a long-lasting period of NPY infusion. This is consistent with the proposal that NPY is a mediator of this sympathetic-evoked vagal attenuation.
在麻醉犬中,研究了长时间静脉输注神经肽Y(NPY,180±8分钟,53±4微克/千克/小时)对心脏交感神经刺激和静脉推注NPY所诱发的心脏迷走神经作用的长期抑制的影响。交感神经刺激和NPY注射在四个不同的时间点进行;一次在对照条件下,然后在NPY输注期的早期和晚期各进行一次,最后一次在NPY输注停止后60 - 90分钟进行。与其他三个注射组相比,在NPY输注后期,注射NPY所诱发的心脏迷走神经作用的最大抑制明显较小(方差分析,P < 0.001)。而且该反应恢复到一半的时间也明显短于其他三个注射组(方差分析,P < 0.001)。与其他三个刺激组相比,在NPY输注后期,交感神经刺激所诱发的心脏迷走神经作用的最大抑制明显降低(方差分析,P < 0.0001)。该反应恢复到一半的时间也短于其他三个刺激组(方差分析,P < 0.001)。结果表明,在长时间的NPY输注期间,迷走神经对外源性NPY和交感神经刺激的衰减发生了脱敏。这与NPY是这种交感神经诱发的迷走神经衰减的介质这一观点一致。