Augmented supraorbital skin sympathetic nerve activity responses to symptom trigger events in rosacea patients

作者：Metzler Wilson Kristen; Toma Kumika; Sammons Dawn L; Mann Sarah; Jurovcik Andrew J; Demidova Olga; Wilson Thad E^*

来源：Journal of Neurophysiology, 2015, 114(3): 1530-1537.

DOI：10.1152/jn.00458.2015

• supraorbital nerve
• rosacea triggers
• mental stress
• physical stress
• heat stress
• autonomic dysfunction
• sympathetic nervous system

Facial flushing in rosacea is often induced by trigger events. However, trigger causation mechanisms are currently unclear. This study tested the central hypothesis that rosacea causes sympathetic and axon reflex-mediated alterations resulting in trigger-induced symptomatology. Twenty rosacea patients and age/sex-matched controls participated in one or a combination of symptom triggering stressors. In protocol 1, forehead skin sympathetic nerve activity (SSNA; supraorbital microneurography) was measured during sympathoexcitatory mental (2-min serial subtraction of novel numbers) and physical (2-min isometric handgrip) stress. In protocol 2, forehead skin blood flow (laser-Doppler flowmetry) and transepithelial water loss/sweat rate (capacitance hygrometry) were measured during sympathoexcitatory heat stress (whole body heating by perfusing 50 degrees C water through a tube-lined suit). In protocol 3, cheek, forehead, forearm, and palm skin blood flow were measured during nonpainful local heating to induce axon reflex vasodilation. Heart rate (HR) and mean arterial pressure (MAP) were recorded via finger photoplethysmography to calculate cutaneous vascular conductance (CVC; flux.100/MAP). Higher patient transepithelial water loss was observed (rosacea 0.20 +/- 0.02 vs. control 0.10 +/- 0.01 mg.cm(-2).min(-1), P < 0.05). HR and MAP changes were not different between groups during sympathoexcitatory stressors or local heating. SSNA during early mental (32 +/- 9 and 9 +/- 4% increase) and physical (25 +/- 4 and 5 +/- 1% increase, rosacea and controls, respectively) stress was augmented in rosacea (both P < 0.05). Heat stress induced more rapid sweating and cutaneous vasodilation onset in rosacea compared with controls. No axon reflex vasodilation differences were observed between groups. These data indicate that rosacea affects SSNA and that hyperresponsiveness to trigger events appears to have a sympathetic component.

• 出版日期2015-9-1