Effects of NSAIDs on the Release of Calcitonin Gene-Related Peptide and Prostaglandin E2 from Rat Trigeminal Ganglia

Nonsteroidal anti-inflammatory drugs (NSAIDs) are frequently used to treat migraine, but the mechanisms of their effects in this pathology are not fully elucidated. The trigeminal ganglia and calcitonin gene-related peptide (CGRP) have been implicated in the pathophysiology of migraine. The release...

Full description

Saved in:
Bibliographic Details
Main Authors: Vittorio Vellani, Giorgia Moschetti, Silvia Franchi, Chiara Giacomoni, Paola Sacerdote, Giada Amodeo
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2017/9547056
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832550055963262976
author Vittorio Vellani
Giorgia Moschetti
Silvia Franchi
Chiara Giacomoni
Paola Sacerdote
Giada Amodeo
author_facet Vittorio Vellani
Giorgia Moschetti
Silvia Franchi
Chiara Giacomoni
Paola Sacerdote
Giada Amodeo
author_sort Vittorio Vellani
collection DOAJ
description Nonsteroidal anti-inflammatory drugs (NSAIDs) are frequently used to treat migraine, but the mechanisms of their effects in this pathology are not fully elucidated. The trigeminal ganglia and calcitonin gene-related peptide (CGRP) have been implicated in the pathophysiology of migraine. The release of CGRP and prostaglandin E2 (PGE2) from freshly isolated rat trigeminal ganglia was evaluated after oral administration of nimesulide, etoricoxib, and ketoprofen, NSAIDs with different pharmacological features. Thirty minutes after oral administration, nimesulide, 10 mg/Kg, decreased the GCRP release induced by an inflammatory soup, while the other NSAIDs were ineffective at this point in time. Two hours after oral nimesulide (5 and 10 mg/Kg) and ketoprofen (10 mg/Kg), but not of etoricoxib, a significant decrease in the CGRP release was observed. All drugs reduced PGE2, although with some differences in timing and doses, and the action on CGRP does not seem to be related to PGE2 inhibition. The reduction of CGRP release from rat trigeminal ganglia after nimesulide and ketoprofen may help to explain the mechanism of action of NSAIDs in migraine. Since at 30 minutes only nimesulide was effective in reducing CGRP release, these results suggest that this NSAID may exert a particularly rapid effect in patients with migraine.
format Article
id doaj-art-38843238de48432785ee5586cff92316
institution Kabale University
issn 0962-9351
1466-1861
language English
publishDate 2017-01-01
publisher Wiley
record_format Article
series Mediators of Inflammation
spelling doaj-art-38843238de48432785ee5586cff923162025-02-03T06:07:45ZengWileyMediators of Inflammation0962-93511466-18612017-01-01201710.1155/2017/95470569547056Effects of NSAIDs on the Release of Calcitonin Gene-Related Peptide and Prostaglandin E2 from Rat Trigeminal GangliaVittorio Vellani0Giorgia Moschetti1Silvia Franchi2Chiara Giacomoni3Paola Sacerdote4Giada Amodeo5Dipartimento di Scienze Biomediche, Metaboliche e Neuroscienze, Università di Modena e Reggio Emilia, Via Campi 287, 41125 Modena, ItalyDipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Via Vanvitelli 32, 20129 Milano, ItalyDipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Via Vanvitelli 32, 20129 Milano, ItalyDipartimento di Economia, Scienze e Diritto, Salita alla Rocca 44, 47890 San Marino, San MarinoDipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Via Vanvitelli 32, 20129 Milano, ItalyDipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Via Vanvitelli 32, 20129 Milano, ItalyNonsteroidal anti-inflammatory drugs (NSAIDs) are frequently used to treat migraine, but the mechanisms of their effects in this pathology are not fully elucidated. The trigeminal ganglia and calcitonin gene-related peptide (CGRP) have been implicated in the pathophysiology of migraine. The release of CGRP and prostaglandin E2 (PGE2) from freshly isolated rat trigeminal ganglia was evaluated after oral administration of nimesulide, etoricoxib, and ketoprofen, NSAIDs with different pharmacological features. Thirty minutes after oral administration, nimesulide, 10 mg/Kg, decreased the GCRP release induced by an inflammatory soup, while the other NSAIDs were ineffective at this point in time. Two hours after oral nimesulide (5 and 10 mg/Kg) and ketoprofen (10 mg/Kg), but not of etoricoxib, a significant decrease in the CGRP release was observed. All drugs reduced PGE2, although with some differences in timing and doses, and the action on CGRP does not seem to be related to PGE2 inhibition. The reduction of CGRP release from rat trigeminal ganglia after nimesulide and ketoprofen may help to explain the mechanism of action of NSAIDs in migraine. Since at 30 minutes only nimesulide was effective in reducing CGRP release, these results suggest that this NSAID may exert a particularly rapid effect in patients with migraine.http://dx.doi.org/10.1155/2017/9547056
spellingShingle Vittorio Vellani
Giorgia Moschetti
Silvia Franchi
Chiara Giacomoni
Paola Sacerdote
Giada Amodeo
Effects of NSAIDs on the Release of Calcitonin Gene-Related Peptide and Prostaglandin E2 from Rat Trigeminal Ganglia
Mediators of Inflammation
title Effects of NSAIDs on the Release of Calcitonin Gene-Related Peptide and Prostaglandin E2 from Rat Trigeminal Ganglia
title_full Effects of NSAIDs on the Release of Calcitonin Gene-Related Peptide and Prostaglandin E2 from Rat Trigeminal Ganglia
title_fullStr Effects of NSAIDs on the Release of Calcitonin Gene-Related Peptide and Prostaglandin E2 from Rat Trigeminal Ganglia
title_full_unstemmed Effects of NSAIDs on the Release of Calcitonin Gene-Related Peptide and Prostaglandin E2 from Rat Trigeminal Ganglia
title_short Effects of NSAIDs on the Release of Calcitonin Gene-Related Peptide and Prostaglandin E2 from Rat Trigeminal Ganglia
title_sort effects of nsaids on the release of calcitonin gene related peptide and prostaglandin e2 from rat trigeminal ganglia
url http://dx.doi.org/10.1155/2017/9547056
work_keys_str_mv AT vittoriovellani effectsofnsaidsonthereleaseofcalcitoningenerelatedpeptideandprostaglandine2fromrattrigeminalganglia
AT giorgiamoschetti effectsofnsaidsonthereleaseofcalcitoningenerelatedpeptideandprostaglandine2fromrattrigeminalganglia
AT silviafranchi effectsofnsaidsonthereleaseofcalcitoningenerelatedpeptideandprostaglandine2fromrattrigeminalganglia
AT chiaragiacomoni effectsofnsaidsonthereleaseofcalcitoningenerelatedpeptideandprostaglandine2fromrattrigeminalganglia
AT paolasacerdote effectsofnsaidsonthereleaseofcalcitoningenerelatedpeptideandprostaglandine2fromrattrigeminalganglia
AT giadaamodeo effectsofnsaidsonthereleaseofcalcitoningenerelatedpeptideandprostaglandine2fromrattrigeminalganglia