Rosenmeier Jaya B, Fritzlar Sandy J, Dinenno Frank A, Joyner Michael J
Department of Anesthesiology, Mayo Clinic, Rochester, MN 55905, USA.
J Appl Physiol (1985). 2003 Dec;95(6):2370-4. doi: 10.1152/japplphysiol.00634.2003. Epub 2003 Aug 15.
Nitric oxide (NO) is capable of blunting alpha-adrenergic vasoconstriction in contracting skeletal muscles of experimental animals (functional sympatholysis). We therefore tested the hypothesis that exogenous NO administration can blunt alpha-adrenergic vasoconstriction in resting human limbs by measuring forearm blood flow (FBF; Doppler ultrasound) and blood pressure in eight healthy males during brachial artery infusions of three alpha-adrenergic constrictors (tyramine, which evokes endogenous norepinephrine release; phenylephrine, an alpha1-agonist; and clonidine, an alpha2-agonist). To simulate exercise hyperemia, the vasoconstriction caused by the alpha-agonists was compared during adenosine-mediated (>50% NO independent) and sodium nitroprusside-mediated (SNP; NO donor) vasodilation of the forearm. Both adenosine and SNP increased FBF from approximately 35-40 to approximately 200-250 ml/min. All three alpha-adrenergic constrictor drugs caused marked reductions in FBF and calculated forearm vascular conductance (P < 0.05). The relative reductions in forearm vascular conductance caused by the alpha-adrenergic constrictors during SNP infusion were similar (tyramine, -74 +/- 3 vs. -65 +/- 2%; clonidine, -44 +/- 6 vs. -44 +/- 6%; P > 0.05) or slightly greater (phenylephrine, -47 +/- 6 vs. -33 +/- 6%; P < 0.05) compared with the responses during adenosine. In conclusion, these results indicate that exogenous NO sufficient to raise blood flow to levels simulating those seen during exercise does not blunt alpha-adrenergic vasoconstriction in the resting human forearm.
一氧化氮(NO)能够减弱实验动物收缩骨骼肌中的α-肾上腺素能血管收缩作用(功能性交感神经阻滞)。因此,我们通过测量八名健康男性在肱动脉输注三种α-肾上腺素能收缩剂(酪胺,可引起内源性去甲肾上腺素释放;去氧肾上腺素,一种α1-激动剂;可乐定,一种α2-激动剂)期间的前臂血流量(FBF;多普勒超声)和血压,来检验外源性给予NO可减弱静息人肢体中α-肾上腺素能血管收缩作用的假设。为了模拟运动性充血,在腺苷介导的(>50%不依赖NO)和硝普钠介导的(SNP;NO供体)前臂血管舒张过程中,比较了α-激动剂引起的血管收缩情况。腺苷和SNP均使FBF从约35 - 40 ml/min增加至约200 - 250 ml/min。所有三种α-肾上腺素能收缩剂药物均导致FBF和计算得出的前臂血管传导率显著降低(P < 0.05)。与腺苷给药期间的反应相比,SNP输注期间α-肾上腺素能收缩剂引起的前臂血管传导率相对降低相似(酪胺,-74±3 vs. -65±2%;可乐定,-44±6 vs. -44±6%;P > 0.05)或稍大(去氧肾上腺素,-47±6 vs. -33±6%;P < 0.05)。总之,这些结果表明,足以将血流量提高至模拟运动时水平的外源性NO并不会减弱静息人前臂中的α-肾上腺素能血管收缩作用。