Local neurogenic regulation of rat hindlimb circulation: CO2‐induced release of calcitonin gene‐related peptide from sensory nerves
Open Access
- 1 October 1997
- journal article
- Published by Wiley in British Journal of Pharmacology
- Vol. 122 (4) , 710-714
- https://doi.org/10.1038/sj.bjp.0701423
Abstract
The mechanism of release of calcitonin gene‐related peptide (CGRP) from sensory nerves in response to skeletal muscle contraction was investigated in the rat hindlimb in vivo and in vitro. In the anaesthetized rat, sciatic nerve stimulation at 10 Hz for 1 min caused a hyperaemic response in the hindlimb. During the response, partial pressure of CO2 in the venous blood effluent from the hindlimb significantly increased from 43±3 to 73±8 mmHg, whereas a small decrease in pH and no appreciable change in partial pressure of O2 were observed. An intra‐arterial bolus injection of NaHCO3 (titrated to pH 7.2 with HCl), which elevated PCO2 of the venous blood, caused a sustained increase in regional blood flow of the iliac artery. Capsaicin (0.33 μmol kg−1, i.a.) and a specific calcitonin gene‐related peptide (CGRP) receptor antagonist, CGRP(8–37), (100 nmol kg−1 min−1, i.v.) significantly suppressed the hyperaemic response to NaHCO3. Neither NDΩ‐nitro‐L‐arginine methyl ester (1 μmol kg−1 min−1, i.v.) nor indomethacin (5 mg kg−1, i.v.) affected the response. The serum level of CGRP‐like immunoreactivity in the venous blood was significantly increased by a bolus injection of NaHCO3 (pH=7.2) from 50±4 to 196±16 fmol ml−1. In the isolated hindlimb perfused with Krebs‐Ringer solution, a bolus injection of NaHCO3 (pH=7.2) caused a decrease in perfusion pressure which was composed of two responses, i.e., an initial transient response and a slowly‐developing long‐lasting one. CGRP(8–37) significantly inhibited the latter response by 73%. These results suggest that CO2 liberated from exercising skeletal muscle activates capsaicin‐sensitive perivascular sensory nerves locally, which results in the release of CGRP from their peripheral endings, and then the released peptide causes local vasodilatation. British Journal of Pharmacology (1997) 122, 710–714; doi:10.1038/sj.bjp.0701423Keywords
This publication has 16 references indexed in Scilit:
- Local neurogenic regulation of rat hindlimb circulation: role of calcitonin gene‐related peptide in vasodilatation after skeletal muscle contractionBritish Journal of Pharmacology, 1997
- Calcitonin gene-related peptide (CGRP) induces more potent vasorelaxation in the resistance portion than in the conduit portion of mesenteric arteries in humansPeptides, 1996
- CGRP (8–37) reduces the duration but not the maximal increase of antidromic vasodilation in dental pulp and lip of the ratActa Physiologica Scandinavica, 1994
- Relative involvement of substance P and CGRP mechanisms in antidromic vasodilation in the rat skinActa Physiologica Scandinavica, 1992
- Release of calcitonin gene-related peptide-like (CGRP-LI) immunoreactivity from rat isolated soleus muscle by low pH, capsaicin and potassiumNeuroscience Letters, 1992
- The pharmacology of the efferent function of sensory nerves.Journal of Autonomic Pharmacology, 1991
- Capsaicin and primary afferent neurons: From basic science to human therapy?Journal of the Autonomic Nervous System, 1991
- Neurogenic vasodilation and release of calcitonin gene-related peptide (CGRP) from perivascular nerves in the rat mesenteric arteryBiochemical and Biophysical Research Communications, 1989
- Characteristics of pressor response to endothelin in spontaneously hypertensive and Wistar-Kyoto rats.Hypertension, 1989
- Sympathetic nerve discharge is coupled to muscle cell pH during exercise in humans.Journal of Clinical Investigation, 1988