Purpose: We investigated the role of noradrenergic sympathetic nerves in the cutaneous circulation at rest and in response to local heating.
Methods: Dorsal forearm and lateral leg sites were each instrumented with 2 microdialysis fibers, 2 local skin heaters, and 2 laser-Doppler probes. All sites were heated from 33° to 42 °C. Each limb had 1 skin site treated with bretylium tosylate (BT) to block noradrenergic sympathetic neurotransmitter release and 1 site infused with lactated Ringer's (Control).
Results: During baseline (33 °C), cutaneous vascular conductance (CVC; laser-Doppler flux/blood pressure) at control (24 ± 2 %max) and BT-treated (29 ± 4 %max) sites in the leg was significantly higher than the forearm (control: 12 ± 1 %max; BT-treated: 17 ± 2 %max) (P = 0.032 and P = 0.042). At 42 °C local skin temperature, the initial peak CVC response with BT decreased compared to control at both forearm (62 ± 3 vs. 86 ± 6 %max, P < 0.01) and leg (67 ± 3 vs. 77 ± 2 %max, P = 0.035) sites. CVC at the forearm with BT was lower than that of the leg (P = 0.02). With control, plateau phase (~35 min at 42 °C) CVC was greater in the leg (98 ± 2 %max) than the forearm (89 ± 4 %max) (P = 0.027). BT reduced the peak CVC in the leg (90 ± 4 %max, P = 0.027) and in the forearm (69 ± 5 %max, P < 0.01). CVC at the BT-treated sites was reduced more in the forearm than in the legs (P < 0.01).
Conclusions: The contribution of noradrenergic sympathetic nerves during local heating differs between leg and forearm at rest and with skin heating.
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http://dx.doi.org/10.1007/s00421-014-3097-1 | DOI Listing |
Nat Rev Cardiol
January 2025
Institute for Pathophysiology, West German Heart and Vascular Center, University of Duisburg-Essen, Essen, Germany.
Am J Physiol Regul Integr Comp Physiol
December 2024
Institute of Health and Sport Sciences, University of Tsukuba, Tsukuba City, Japan.
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 remains 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.
View Article and Find Full Text PDFMov Disord Clin Pract
December 2024
Department of Neurology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
Background: The role played by sympathetic and parasympathetic autonomic branches in patients with Parkinson's disease carrying variants in the GBA1 gene (GBA-PD) is still elusive.
Objectives: To characterize cardiovascular autonomic function in GBA-PD and I-PD patients with early and mid-stage disease.
Methods: These assessments were performed: cardiovascular autonomic tests, analysis of heart rate and blood pressure variability, cardiac noradrenergic imaging.
J Neurotrauma
December 2024
Department of Biological Sciences, College of Science, National Sun Yat-sen University, Kaohsiung, Taiwan.
Cervical spinal cord injury usually leads to cardiorespiratory dysfunction due to interruptions of the supraspinal pathways innervating the phrenic motoneurons and thoracic sympathetic preganglionic neurons. Although clinical guidelines recommend maintaining the mean arterial pressure within 85-90 mmHg during the first week of injury, there is no pre-clinical evidence from animal models to prove the therapeutic efficacy of hemodynamic management. Accordingly, the present study was designed to investigate the therapeutic efficacy of hemodynamic management in rats with cervical spinal cord contusion.
View Article and Find Full Text PDFClin Auton Res
December 2024
Autonomic Medicine Section (AMS), Clinical Neurosciences Program (CNP), Division of Intramural Research (DIR), National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health (NIH), 10 Center Drive MSC-1620, Building 10 Room 8N260, Bethesda, MD, 20892-1620, USA.
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