1997
DOI: 10.1097/00006123-199703000-00027
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Role of Nitric Oxide in Cutaneous Blood Flow Increases in the Rat Hindpaw during Dorsal Column Stimulation

Abstract: Our results demonstrated that nitric oxide played a significant role in producing the DCS-induced increase in rat cutaneous hindpaw blood flow. The involvement of nitric oxide does not require the presence of autonomic efferent function; however, ganglionic blockade may unmask a mechanism for vasodilation during DCS that is independent of nitric oxide release.

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Cited by 21 publications
(16 citation statements)
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“…The underlying mechanisms are thought to involve alterations in peripheral sympathetic tone and the release of vasodilators. 3,19 The effects of SCS on CBF have also been observed in isolated cases and small clinical series. 10,11,23,27,35 A scientific basis for these observations and the underlying mechanism(s) has yet to be well delineated.…”
Section: Discussionmentioning
confidence: 97%
“…The underlying mechanisms are thought to involve alterations in peripheral sympathetic tone and the release of vasodilators. 3,19 The effects of SCS on CBF have also been observed in isolated cases and small clinical series. 10,11,23,27,35 A scientific basis for these observations and the underlying mechanism(s) has yet to be well delineated.…”
Section: Discussionmentioning
confidence: 97%
“…Electrotherapy, in particular in the form of SCS, enhances the blood flow in ischemic peripheral vascular and coronary heart disease [41]. The vasodilation may be induced by release of vasoactive substances such as calcitonin gene-related peptide and possibly nitric oxide (NO) [42,43,44]. In certain conditions an inhibition of sympathetic afferent activity may contribute to vasodilation [45].…”
Section: Circulatory Effects Of Electrotherapymentioning
confidence: 99%
“…Spinal cord stimulation reduces pain in Buerger's disease by promoting the secretion of gamma-aminobutyric acid (GABA), serotonin, and substance P at the spinal nerve dorsal horn. In addition, it inhibits nociceptive neurotransmission, and intramedullary oxidative nitric oxide and GABA act as an important mediator for the induction of pain relief after spinal cord stimulation [11-13]. Spinal cord stimulation in peripheral obstructive arterial disease can treat chronic ischemic pain and ulcers and also prevent amputation.…”
Section: Discussionmentioning
confidence: 99%