Separate and combined blockades of α- and β-adrenergic receptors in forearm sweating induced by adrenergic agents and exercise in the heat in young adults.

IF 2.2 3区 医学 Q3 PHYSIOLOGY
Tatsuro Amano, Naoto Fujii, Glen P Kenny, Toby Mündel, Yoshimitsu Inoue, Shotaro Yokoyama, Narihiko Kondo
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引用次数: 0

Abstract

The assessment of adrenergic modulation of sweating as assessed via pharmacologic administration of α- and β-adrenergic receptor blockers during exercise has yielded mixed findings. However, the underlying mechanisms for this disparity remain unresolved. We investigated the effects of separate and combined blockade of α- and β-adrenergic receptors on forearm sweating induced by a 30-min moderate-intensity exercise bout (n = 17, protocol 1) and the administration of adrenergic agonists epinephrine and norepinephrine (n = 16, protocol 2) in the heat. Adrenergic receptor blockade was induced via the separate and combined iontophoretic administration of terazosin (α-adrenergic receptor antagonist) and propranolol (β-adrenergic receptor antagonist) on forearm skin. Bretylium, a noradrenergic sympathetic nerve inhibitor, was also administered separately in protocol 1. In protocol 1, relative to the separate administration of propranolol, terazosin alone or in combination with propranolol attenuated exercise sweating to a similar extent (both P ≤ 0.037), although the effect was reduced relative to that observed with bretylium treatment (P < 0.001). In protocol 2, administration of propranolol increased norepinephrine- (P = 0.029) but not epinephrine-induced sweat rate. The combined administration of terazosin reversed this response, attenuating sweating (P < 0.001) to a greater extent than terazosin treatment alone (P = 0.030). Altogether, we showed that although β-adrenergic receptors may interact with α-adrenergic receptors pharmacologically, it does not appear to modulate exercise-induced sweating on the forearm. Furthermore, α- but not β-adrenergic receptors independently modulate the regulation of forearm sweating during exercise in the heat. Finally, the bretylium-induced reduction in forearm sweat rate during exercise likely occurs independently of α- and β-adrenergic receptors.NEW & NOTEWORTHY Pharmacological stimulation of α- and β-adrenergic receptors produces sweating in vivo. Still, the separate and interactive roles of these adrenergic receptors during exercise and pharmacological adrenergic stimulation in the heat remain unknown. We showed that β-adrenergic receptors may interact with α-adrenergic receptors pharmacologically, but it does not modulate exercise-induced sweating. The α-adrenergic receptors independently modulate sweating during exercise in the heat. We provide important new insights into our understanding of the mechanisms regulating human sweating.

肾上腺素能药物和高温运动诱导的前臂出汗α-和β-肾上腺素能受体的单独和联合阻断
通过在运动中使用α-和β-肾上腺素受体阻滞剂来评估肾上腺素能对出汗的调节,得出了不同的结果。然而,造成这种差异的根本机制仍未得到解决。我们研究了单独和联合阻断α-和β-肾上腺素受体对30分钟中等强度运动(n=17,方案1)和肾上腺素受体激动剂肾上腺素和去甲肾上腺素(n=16,方案2)在高温下引起的前臂出汗的影响。将特拉唑嗪(α-肾上腺素能受体拮抗剂)和心得安(β-肾上腺素能受体拮抗剂)分别或联合离子吸氧给药于前臂皮肤,诱导肾上腺素能受体阻断。Bretylium,一种去肾上腺素能交感神经抑制剂,也在方案1中单独给予。在方案1中,相对于单独给药心得安,特拉唑嗪单独或与心得安联合减少运动出汗的程度相似(P值均为0.037),尽管效果相对于布雷利姆治疗(PP=0.029)有所降低,但肾上腺素诱导的出汗率没有降低。联合使用特拉唑嗪逆转了这种反应,减少了出汗(PP=0.030)。总之,我们表明,虽然β-肾上腺素能受体可能与α-肾上腺素能受体在药理学上相互作用,但它似乎不会调节前臂运动引起的出汗。此外,α-而非β-肾上腺素能受体独立调节高温运动时前臂出汗的调节。最后,布雷利姆诱导的运动期间前臂出汗率的降低可能独立于α-和β-肾上腺素能受体发生。
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来源期刊
CiteScore
5.30
自引率
3.60%
发文量
145
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Regulatory, Integrative and Comparative Physiology publishes original investigations that illuminate normal or abnormal regulation and integration of physiological mechanisms at all levels of biological organization, ranging from molecules to humans, including clinical investigations. Major areas of emphasis include regulation in genetically modified animals; model organisms; development and tissue plasticity; neurohumoral control of circulation and hypertension; local control of circulation; cardiac and renal integration; thirst and volume, electrolyte homeostasis; glucose homeostasis and energy balance; appetite and obesity; inflammation and cytokines; integrative physiology of pregnancy-parturition-lactation; and thermoregulation and adaptations to exercise and environmental stress.
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