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Published in: The Journal of Headache and Pain 1/2014

Open Access 01-12-2014 | Research article

Release of CGRP from mouse brainstem slices indicates central inhibitory effect of triptans and kynurenate

Authors: Charlotte Kageneck, Barbara E Nixdorf-Bergweiler, Karl Messlinger, Michael JM Fischer

Published in: The Journal of Headache and Pain | Issue 1/2014

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Abstract

Background

CGRP is contained in a substantial proportion of unmyelinated trigeminal neurons innervating intracranial tissues. Previously, we have described a hemisected rodent scull preparation and later the intact trigeminal ganglion to measure stimulated CGRP release from trigeminal afferents.

Methods

Here, we establish a preparation for examining CGRP release from central trigeminal terminals using single fresh slices of the mouse medullary brainstem.

Results

Basal and stimulated amount of CGRP substantially exceeded the detection level. Experiments were designed as matched pairs of at least six brainstem slices per animal. Stimulation with high potassium induced calcium-dependent and reversible CGRP release. Capsaicin stimulation of TRPV1 provoked concentration-dependent CGRP release. The anti-migraine drug naratriptan did not inhibit capsaicin-induced CGRP release from peripheral terminals but inhibited the release from brainstem slices. The glutamate antagonist kynurenate showed a similar pattern of site-specific inhibition of CGRP release.

Conclusions

As observed earlier for other drugs used in the treatment of migraine this indicates that the central terminals in the spinal trigeminal nucleus may be the main site of action. The preparation allows evaluating the trigeminal brainstem as a pharmacological site of action.
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Metadata
Title
Release of CGRP from mouse brainstem slices indicates central inhibitory effect of triptans and kynurenate
Authors
Charlotte Kageneck
Barbara E Nixdorf-Bergweiler
Karl Messlinger
Michael JM Fischer
Publication date
01-12-2014
Publisher
Springer Milan
Published in
The Journal of Headache and Pain / Issue 1/2014
Print ISSN: 1129-2369
Electronic ISSN: 1129-2377
DOI
https://doi.org/10.1186/1129-2377-15-7

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