dc.contributor.author |
Guerrero-Toro C. |
|
dc.contributor.author |
Timonina A. |
|
dc.contributor.author |
Gubert-Olive M. |
|
dc.contributor.author |
Giniatullin R. |
|
dc.date.accessioned |
2018-09-19T23:11:56Z |
|
dc.date.available |
2018-09-19T23:11:56Z |
|
dc.date.issued |
2016 |
|
dc.identifier.issn |
2191-1630 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/146049 |
|
dc.description.abstract |
© 2016, Springer Science+Business Media New York.The monoamine neurotransmitter serotonin (5-HT) and the neuropeptide calcitonin gene-related peptide (CGRP) play an important role in migraine pathophysiology. To study potential interplay between 5-HT and CGRP in peripheral trigeminal nociception, we performed calcium imagining and patch clamp studies in rat trigeminal ganglia cells. We found that 5-HT activated Ca2+ transients in 18 % of trigeminal ganglia neurons. Exposure of trigeminal cells to CGRP significantly increased the number of 5-HT positive cells to 35 % and increased the amplitude of 5-HT-induced Ca2+ transients. Using patch clamp technique, we show that 37 % percent of trigeminal cells generated desensitizing membrane currents suggesting functional expression of 5-HT3 receptors. These responses were partially co-localized either with ATP-gated or capsaicin-sensitive neurons. Exposure to CGRP for 2 h increased the current density in the ATP-sensitive fraction of trigeminal neurons. Taken together, these data suggest that 5-HT receptor sensitization contributes to the pro-nociceptive effect of CGRP in trigeminal neurons. |
|
dc.relation.ispartofseries |
BioNanoScience |
|
dc.subject |
CGRP |
|
dc.subject |
Migraine |
|
dc.subject |
Serotonin |
|
dc.subject |
Trigeminal neurons |
|
dc.subject |
TRPV1 |
|
dc.title |
Facilitation of Serotonin-Induced Signaling by the Migraine Mediator CGRP in Rat Trigeminal Neurons |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
4 |
|
dc.relation.ispartofseries-volume |
6 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
357 |
|
dc.source.id |
SCOPUS21911630-2016-6-4-SID84999828367 |
|