Dual capsaicin effects on ureteric motility: low dose inhibition mediated by calcitonin gene‐related peptide and high dose stimulation by tachykinins?
- 1 November 1986
- journal article
- Published by Wiley in Acta Physiologica Scandinavica
- Vol. 128 (3) , 453-465
- https://doi.org/10.1111/j.1748-1716.1986.tb07999.x
Abstract
The effects of capsaicin, in relation to substance P (SP), neurokinin A (NKA), neuropeptide K (NPK) and calcitonin gene‐related peptide (CGRP) which coexist in local sensory nerves, on the motility of the guinea‐pig ureter were studied in vivo and in vitro. Capsaicin in a low dose (ionmolkg‐1) given i.v. inhibited spontaneous, peristaltic contractions, as revealed by perfusion‐pressure changes of the constantly perfused ureter in vivo. This action was independent of autonomic reflexes and prostaglandin formation. Capsaicin stimulated ureteric motility at higher doses (100 and 500 nmol kg‐1). The dual effects of capsaicin on the ureteric contractility were absent 2 weeks after systemic capsaicin treatment, which depletes sensory neuropeptides. Both NKA and NPK initiated, as well as increased, the magnitude of the peristaltic contractions of the ureter, while SP only caused a minor excitatory effect. The CGRP inhibited spontaneous, as well as NKA‐ and NPK‐induced ureteric peristaltic contractions. In vitro experiments on the ureter revealed that capsaicin (10‐6 M) induced phasic circular muscle contractions in 60% of the experiments. Neurokinin A, NPK and SP consistently increased the contractile activity. The NKA tachyphylaxis inhibited the contractile response to other tachykinins and capsaicin. The SP analogue Spantide (/D‐Arg1, D‐Trp7,9, Leu11/‐SP) inhibited the contractile responses to SP, NKA and NPK. The CGRP also inhibited the NKA‐ and NPK‐induced contractions of the ureter in vitro. In conclusion, capsaicin, which induces the release of mediators from sensory nerves within the ureter, has either stimulatory or inhibitory effects on ureteric smooth muscle, depending on the in vivo dose administered. The inhibitory response at a low capsaicin dose is similar to the effect of CGRP, while the contractile effects at higher doses resemble the response to tachykinins.Keywords
This publication has 42 references indexed in Scilit:
- Inflammatory oedema induced by synergism between calcitonin gene‐related peptide (CGRP) and mediators of increased vascular permeabilityBritish Journal of Pharmacology, 1985
- Calcitonin gene-related peptide (CGRP) and capsaicin-induced stimulation of heart contractile rate and forceNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1985
- Potentiation of tachykinin-induced plasma protein extravasation by calcitonin gene-related peptideEuropean Journal of Pharmacology, 1985
- Perivascular peptides relax cerebral arteries concomitant with stimulation of cyclic adenosine monophosphate accumulation or release of an endothelium-derived relaxing factor in the catNeuroscience Letters, 1985
- Calcitonin gene-related peptide is a potent vasodilatorNature, 1985
- Systemic capsaicin treatment impairs the micturition reflex in the ratBritish Journal of Pharmacology, 1984
- Rapid degradation of [3H]‐substance P in guinea‐pig ileum and rat vas deferens in vitroBritish Journal of Pharmacology, 1983
- Contractile Effects of Some Polypeptides on the Isolated Urinary Bladder of Guinea‐pig, Rabbit, and RatActa Pharmacologica et Toxicologica, 1982
- Capsaicin: A Chemical Probe for Sensory Neuron MechanismsPublished by Springer Nature ,1982
- Immunoreactive substance P in sympathetic ganglia: Distribution and sensitivity towards capsaicinNeuroscience, 1981