• Charlotte Kageneck, Barbara E Nixdorf-Bergweiler, Karl Messlinger, and Michael Jm Fischer.
• Institute of Physiology and Pathophysiology, University of Erlangen-Nuremberg, Universitaetsstrasse, 91054 Erlangen, Germany. fischer@physiologie1.uni-erlangen.de.
• J Headache Pain. 2014 Feb 8; 15: 7.

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