1987
DOI: 10.1016/0304-3959(87)90139-4
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Release of substance P from peripheral nerve terminals following electrical stimulation of the sciatic nerve

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Cited by 15 publications
(17 citation statements)
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“…The nerve fibres can also be seen to branch from the dermal fibres into the epithelium. Electrical stimulation of the sciatic nerve resulted in a significant increase in SP-like immunoreactivity in the perfusate of the subcutaneous space in the instep of the rat hind paw, as 11 shown in Figure 5, or in blister fluid of the rat hind paw, and this increase was abolished by neonatal pretreatment of rats with capsaicin (White & Helme, 1985). Treatment of newborn rats with capsaicin results in selective and permanent degeneration of small-diameter afferent fibres and significant decrease in the SP content (Jancso et al, 1980) and capsaicintreated animals show significantly increased latencies in response to a noxious thermal stimulus in either the tail-ffick or hot-plate test (Nagy et al, 1980).…”
Section: Effect Of Electrical Stimulation Of the Sciatic Nerve On Cutmentioning
confidence: 84%
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“…The nerve fibres can also be seen to branch from the dermal fibres into the epithelium. Electrical stimulation of the sciatic nerve resulted in a significant increase in SP-like immunoreactivity in the perfusate of the subcutaneous space in the instep of the rat hind paw, as 11 shown in Figure 5, or in blister fluid of the rat hind paw, and this increase was abolished by neonatal pretreatment of rats with capsaicin (White & Helme, 1985). Treatment of newborn rats with capsaicin results in selective and permanent degeneration of small-diameter afferent fibres and significant decrease in the SP content (Jancso et al, 1980) and capsaicintreated animals show significantly increased latencies in response to a noxious thermal stimulus in either the tail-ffick or hot-plate test (Nagy et al, 1980).…”
Section: Effect Of Electrical Stimulation Of the Sciatic Nerve On Cutmentioning
confidence: 84%
“…SP immunofluorescent fibres in the skin were found in unmyelinated primary sensory neurones terminating around the small blood vessels in the dermis and epithelium. Moreover, electrical stimulation of the smalldiameter afferent fibres was shown to induce release of SP in the periphery (Olgart et al, 1977;White & Helme, 1985), and to produce the same cutaneous vasodilatation and plasma extravasation , as after intradermal or intra-arterial administration of SP (Hagermark et al, 1978;Lembeck & Holzer, 1979). These findings suggest that afferent impulses from nerve terminals of small-diameter afferent fibres generated by noxious stimuli may cause release of SP, which may finally control the inflammatory response through regulation of the microcirculation.…”
Section: Introductionmentioning
confidence: 82%
“…Small-diameter primary afferent fibres not only transmit nociceptive messages to central neurons, but are also involved in inflammatory response, such as peripheral neurogenic inflammation (White and Helme, 1985). Following noxious stimulation, these fibres release substance P (SP) and calcitonin gene-related peptide (CGRP), related to oedema and plasma leakage (Basile et al, 1993).…”
Section: Introductionmentioning
confidence: 99%
“…However, it becomes Phe in substance P (SP; 11 amino acids), lie in eledoisin (11 amino acids) and Tyrin physalemin (11 amino acids) [1], Until now, three receptor subtypes of TKs have been identified: the NKi, NK.2 and NK3 inflammation is made highly apparent in ex periments where antidromic stimulation of sensory nerves produces inflammation of the innervated areas [6] by releasing neuropep tides, such as SP, NKA, the vasoactive intesti nal peptide (VIP) or the calcitonin generelated peptide (CGRP) [6][7][8]. These data are confirmed by the use of pharmacological tools such as capsaicin or resiniferatoxin [9,10].…”
Section: Introductionmentioning
confidence: 99%