Nitric oxide and sensory nerves are involved in the vasodilator response to acetylcholine but not calcitonin gene‐related peptide in rat skin micro vasculature
Open Access
- 19 July 1992
- journal article
- Published by Wiley in British Journal of Pharmacology
- Vol. 106 (3) , 650-655
- https://doi.org/10.1111/j.1476-5381.1992.tb14390.x
Abstract
1 The contributions of sensory nerves and nitric oxide (NO) to vasodilator responses to acetylcholine (ACh) and calcitonin gene-related peptide (CGRP) were examined in rat skin microvasculature with a laser Doppler flowmeter to monitor relative blood flow. 2 Perfusion of ACh (100 μm; for 30 min) over a blister base on the rat hind footpad elicited microvascular vasodilatation and this response was not sustained. CGRP (1 μm; 10 min perfusion) also elicited vasodilatation and this response was maintained even when CGRP was no longer in contact with the blister base. 3 The vasodilator response to ACh was significantly smaller in rats pretreated as neonates with capsaicin to destroy primary sensory afferents than it was in age-matched controls. The vasodilator response to CGRP was unaffected by capsaicin pretreatment. 4 Selective inhibitors of NO synthase, NG-nitro-l-arginine (l-NOARG) and NG-monomethyl-l-arginine (l-NMMA) (both at 100 μm) attenuated the vasodilator response to ACh in control rats, but had no effect on the vasodilator response to CGRP. There was a significant l-NOARG-resistant component in control rats while in capsaicin-treated rats the vasodilator response to ACh was virtually abolished by l-NOARG. The inactive stereoisomer NG-monomethyl-d-arginine (100 μm) did not affect the vasodilator response to ACh. 5 The efficacy of l-NOARG and l-NMMA as inhibitors of endothelium-dependent responses was confirmed by use of an endothelium-dependent vasodilator, the calcium ionophore A23187 (100 μm; 10 min perfusion). Vasodilatation to A23187 was strongly attenuated by both l-NOARG and l-NMMA. 6 These results suggest that sensory nerves and NO are both involved in the dilatation produced by ACh in rat skin microvasculature. A component of the vasodilator response elicited by ACh involves a direct action on the microvascular endothelium with subsequent generation of NO, while an additional component is elicited via activation of sensory nerves. The vasodilator mediator(s) released by ACh from sensory nerves acts largely independently of NO. 7 The vasodilator response to CGRP is independent of a prejunctional action on sensory nerves and of NO.Keywords
This publication has 41 references indexed in Scilit:
- Nitric oxide requirement for vasomotor nerve‐induced vasodilation and modulation of resting blood flow in muscle microcirculationActa Physiologica Scandinavica, 1991
- Mechanism of the Hypertension Produced by Inhibition of Nitric Oxide Biosynthesis in RatsJournal of Cardiovascular Pharmacology, 1991
- Synthesis of a nitric oxide-like factor from L-arginine by rat serosal mast cells: Stimulation of guanylate cyclase and inhibition of platelet aggregationBiochemical and Biophysical Research Communications, 1990
- L-arginine availability determines the duration of acetylcholine-induced systemic vasodilatation in vivoBiochemical and Biophysical Research Communications, 1989
- Involvement of capsaicin-sensitive afferent nerve fibres in serotonin-induced plasma extravasation and vasodilatation in rat skinNeuroscience Letters, 1989
- Neurogenic vasodilation in the rat hairy skin measured using a laser Doppler flowmeterLife Sciences, 1989
- L-arginine is the physiological precursor for the formation of nitric oxide in endothelium-dependent relaxationBiochemical and Biophysical Research Communications, 1988
- Quantitative objective assessment of peripheral nociceptive C fibre function.Journal of Neurology, Neurosurgery & Psychiatry, 1988
- Calcitonin gene-related peptide is a potent vasodilatorNature, 1985
- Pharmacologically induced selective degeneration of chemosensitive primary sensory neuronesNature, 1977