In Vivo Release of Calcitonin Gene-related Peptide-like Material from the Cervicotrigeminal Area in the Rat. Effects of Electrical and Noxious Stimulations of the Muzzle
Overview
Affiliations
The continuous perfusion with an artificial cerebrospinal fluid of the cervicotrigeminal area of the spinal cord in halothane-anaesthetized rats allowed the collection of calcitonin gene-related peptide-like material with the same immunological and chromatographic characteristics as authentic rat alpha-calcitonin gene-related peptide. The spinal release of calcitonin gene-related peptide-like material could be significantly increased by the local application of 60 mM K+ (approximately +100%), high-intensity percutaneous electrical stimulation (approximately +200%) and noxious heat (by immersion in water at 52 degrees C; approximately +150%) applied to the muzzle. By contrast, noxious mechanical (pinches) and chemical (subcutaneous formalin injection) stimulations and deep cooling (by immersion in water at 0 degrees C) of the muzzle did not alter the spinal release of calcitonin gene-related peptide-like material. In addition, low-intensity electrical stimulation, recruiting only the A alpha/beta primary afferent fibres, significantly reduced (approximately -30%) the release of calcitonin gene-related peptide-like material from the cervicotrigeminal area. These data suggest that among the various types of natural noxious stimuli, noxious heat may selectively excite calcitonin gene-related peptide-containing A delta and C primary afferent fibres projecting within the dorsal horn of the spinal cord, and that activation of A alpha/beta fibres reduces spontaneous calcitonin gene-related peptide-like material release possibly through an inhibitory presynaptic control of calcitonin gene-related peptide-containing A delta/C fibres.
Humphries S, Johnson M, Long N Percept Psychophys. 1996; 58(5):693-703.
PMID: 8710448 DOI: 10.3758/bf03213101.
Collin E, Frechilla D, Pohl M, Bourgoin S, Mauborgne A, Hamon M Naunyn Schmiedebergs Arch Pharmacol. 1994; 349(4):387-93.
PMID: 7520130 DOI: 10.1007/BF00170885.