Pernow J, Lundberg J M, Kaijser L
Department of Pharmacology, Karolinska Institute, Stockholm, Sweden.
Clin Physiol. 1989 Feb;9(1):67-75. doi: 10.1111/j.1475-097x.1989.tb00957.x.
Neuropeptide Y (NPY) has recently been shown be co-released with noradrenaline (NA) from sympathetic nerves and to cause arterial vasoconstriction in experimental animals and man. The effect of a single oral dose (10 mg capsule) of nifedipine on NPY- and NA-induced reductions of forearm blood flow (FBF) was studied in seven healthy volunteers. Intra-arterial infusions of NPY and NA into the brachial artery before nifedipine caused dose-dependent reductions in FBF with threshold doses of 0.2 and 0.03 nmol x min-1, respectively. The response to NPY was slower in onset and more long lasting than that to NA. Forty-five min after administration of nifedipine, FBF and heart rate had increased significantly (by 49% and seven beats x min-1, respectively, P less than 0.001), while no significant change was observed in systemic blood pressure. The NPY-induced decrease in FBF was slightly but significantly attenuated after compared to before nifedipine (19 +/- 6 vs. 28 +/- 5% at 1.0 nmol NPY x min-1; P less than 0.01). The response to NA was, however, not significantly altered by nifedipine. In conclusion, the NPY-induced reduction in FBF in man was only slightly prevented and the NA response not significantly affected by oral nifedipine administration in a clinically used dose. This suggests that this calcium antagonist, in the present dosage, does not, to any major extent, inhibit the vasoconstrictor effect of NPY or NA in man in vivo.
最近研究表明,神经肽Y(NPY)可与去甲肾上腺素(NA)从交感神经共同释放,并在实验动物和人体中引起动脉血管收缩。本研究在7名健康志愿者中,观察了口服单次剂量(10mg胶囊)硝苯地平对NPY和NA诱导的前臂血流量(FBF)降低的影响。在服用硝苯地平前,经肱动脉向体内动脉内输注NPY和NA,可引起FBF呈剂量依赖性降低,其阈剂量分别为0.2和0.03nmol·min-1。NPY引起的反应起效较慢,持续时间较长。服用硝苯地平45分钟后,FBF和心率显著增加(分别增加49%和7次·min-1,P<0.001),而全身血压无显著变化。与服用硝苯地平前相比,NPY诱导的FBF降低稍有但显著减弱(1.0nmol NPY·min-1时,分别为19±6%和28±5%;P<0.01)。然而,硝苯地平对NA的反应无显著改变。总之,在人体中,口服临床常用剂量的硝苯地平仅轻微阻止了NPY诱导的FBF降低,对NA反应无显著影响。这表明,在当前剂量下,这种钙拮抗剂在很大程度上并不抑制人体体内NPY或NA的血管收缩作用。