Supiano M A, Hogikyan R V, Stoltz A M, Orstan N, Halter J B
Department of Internal Medicine, University of Michigan, Ann Arbor.
Am J Physiol. 1991 Apr;260(4 Pt 1):E599-607. doi: 10.1152/ajpendo.1991.260.4.E599.
Decreased adrenergic responsiveness in human aging could be a result of downregulation mediated by the age-related increase in sympathetic nervous system (SNS) tone. If so, suppression of SNS tone in elderly subjects should upregulate adrenergic responsiveness into the range observed for younger subjects. To test this hypothesis, we examined alpha 1 (phenylephrine)- and alpha 2 (clonidine)-adrenergic agonist-mediated venoconstriction in a group of 15 older healthy subjects (age 59-73 yr) during placebo and when SNS tone was suppressed by guanadrel (15 mg twice daily for 3 wk). During guanadrel compared with placebo 1) there were decreases in plasma norepinephrine (NE) levels (1.47 +/- 0.07 to 0.80 +/- 0.06 nM; P less than 0.001) and in the extravascular NE release rate derived from [3H]NE kinetics (11.8 +/- 1.4 to 6.1 +/- 1.0 nmol.min-1.m-2; P = 0.01), suggesting suppression of SNS tone; 2) there was an augmented clonidine-mediated venoconstriction response [analysis of variance (ANOVA) P = 0.01]; and 3) there was no detectable change in phenylephrine-mediated venoconstriction (ANOVA P = 0.60). When compared with previous results from young subjects, maximal alpha 2-adrenergic venoconstriction during guanadrel was decreased in the elderly compared with the young, although their response appeared to be appropriately upregulated by the decrease in SNS tone. The lack of an age-related decrease in alpha 1-adrenergic venoconstriction, together with the lack of upregulation of this response during guanadrel, suggests that regulation of this alpha 1-adrenergic response is impaired in the older group.
人类衰老过程中肾上腺素能反应性降低可能是由交感神经系统(SNS)张力随年龄增长而增加所介导的下调作用导致的。如果是这样,抑制老年受试者的SNS张力应该会使肾上腺素能反应性上调至年轻受试者的水平。为了验证这一假设,我们在一组15名健康老年受试者(年龄59 - 73岁)中,分别在服用安慰剂期间以及服用胍那决尔(每日两次,每次15 mg,共3周)以抑制SNS张力时,检测了α1(去氧肾上腺素)和α2(可乐定)肾上腺素能激动剂介导的静脉收缩情况。与安慰剂相比,服用胍那决尔时:1)血浆去甲肾上腺素(NE)水平降低(从1.47±0.07降至0.80±0.06 nM;P<0.001),且从[3H]NE动力学得出的血管外NE释放率降低(从11.8±1.4降至6.1±1.0 nmol·min-1·m-2;P = 0.01),提示SNS张力受到抑制;2)可乐定介导的静脉收缩反应增强[方差分析(ANOVA)P = 0.01];3)去氧肾上腺素介导的静脉收缩未检测到变化(ANOVA P = 0.60)。与年轻受试者先前的结果相比,老年受试者在服用胍那决尔时最大α2肾上腺素能静脉收缩较年轻受试者降低了,尽管他们的反应似乎因SNS张力降低而得到了适当上调。α1肾上腺素能静脉收缩缺乏与年龄相关的降低,以及在服用胍那决尔时该反应缺乏上调,提示老年组中该α1肾上腺素能反应调节受损。