Institute for Exercise and Environmental Medicine, Texas Health Presbyterian Hospital Dallas, 7232 Greenville Ave., Dallas, TX 75231, USA.
Am J Physiol Regul Integr Comp Physiol. 2010 May;298(5):R1417-20. doi: 10.1152/ajpregu.00846.2009. Epub 2010 Mar 17.
Cutaneous vasodilation associated with whole-body heat stress occurs via withdrawal of adrenergic vasoconstriction and engagement of cholinergic "active" vasodilation, the latter of which attenuates cutaneous vasoconstrictor responsiveness. However, the precise neurotransmitter(s) responsible for this sympatholytic-like effect remain unknown. In skeletal muscle, ATP inhibits adrenergically mediated vasoconstriction. ATP also may be responsible for attenuating cutaneous vasoconstriction since it is co-released from cholinergic neurons. The effect of ATP on cutaneous vasoconstrictor responsiveness, however, has not been investigated. Accordingly, this study tested the hypothesis that ATP inhibits adrenergically mediated cutaneous vasoconstriction. To accomplish this objective, four microdialysis probes were inserted in dorsal forearm skin of 11 healthy individuals (mean +/- SD; 35 +/- 11 years). Local temperature at each site was clamped at 34 degrees C throughout the protocol. Skin blood flow was indexed by laser-Doppler flowmetry and was used to calculate cutaneous vascular conductance (CVC; laser-Doppler-derived flux/mean arterial pressure), which was normalized to peak CVC achieved with sodium nitroprusside infusion combined with local skin heating to approximately 42 degrees C. Two membranes were perfused with 30 mM ATP, while the other two membranes were flow matched via administration of 2.8 mM adenosine to serve as control sites. After achieving stable baselines, 1 x 10(-4) M tyramine was administered at all sites, while ATP and adenosine continued to be infused at their respective sites. ATP and adenosine infusion increased CVC from baseline by 35 +/- 26% CVC(peak) units and by 36 +/- 15% CVC(peak) units, respectively (P = 0.75). Tyramine decreased CVC similarly (by about one-third) at all sites (P < 0.001 for main effect and P = 0.32 for interaction). These findings indicate that unlike in skeletal muscle, ATP does not attenuate tyramine-stimulated vasoconstriction in human skin.
皮肤血管舒张与全身热应激有关,是通过肾上腺素能血管收缩的撤出和胆碱能“活性”血管舒张的参与来实现的,后者可减弱皮肤血管收缩器的反应性。然而,负责这种类似交感神经抑制作用的确切神经递质仍不清楚。在骨骼肌中,ATP 抑制肾上腺素能介导的血管收缩。由于它是从胆碱能神经元共同释放的,因此 ATP 也可能负责减轻皮肤血管收缩。然而,ATP 对皮肤血管收缩器反应性的影响尚未得到研究。因此,本研究检验了一个假设,即 ATP 抑制肾上腺素能介导的皮肤血管收缩。为了实现这一目标,将四个微透析探针插入 11 名健康个体(平均 +/- SD;35 +/- 11 岁)的背部前臂皮肤中。在整个方案中,每个部位的局部温度均保持在 34 摄氏度。通过激光多普勒流量计测量皮肤血流量,并用于计算皮肤血管传导率(激光多普勒衍生的通量/平均动脉压),该值归一化为用硝普钠输注和局部皮肤加热至约 42 摄氏度联合作用下达到的峰值皮肤血管传导率。两个膜用 30mM ATP 灌注,而另外两个膜通过给予 2.8mM 腺苷进行流量匹配,作为对照部位。在达到稳定基线后,在所有部位给予 1x10(-4)M 酪胺,同时继续在各自部位输注 ATP 和腺苷。ATP 和腺苷输注使 CVC 从基线增加 35 +/- 26% CVC(峰值)单位和 36 +/- 15% CVC(峰值)单位,分别为(P=0.75)。在所有部位,酪胺同样降低 CVC(约三分之一)(主效应 P<0.001,交互作用 P=0.32)。这些发现表明,与骨骼肌不同,ATP 不会减弱人皮肤中酪胺刺激的血管收缩。