Egyszerű nézet

dc.contributor.author Heinzlmann, Andrea
dc.contributor.author Tóth, Zsuzsanna
dc.contributor.author Köves, Katalin
dc.date.accessioned 2016-10-13T06:54:20Z
dc.date.available 2016-10-13T06:54:20Z
dc.date.issued 2011
dc.identifier 79951579774
dc.identifier.citation pagination=101-108; journalVolume=43; journalIssueNumber=1; journalTitle=JOURNAL OF MOLECULAR NEUROSCIENCE;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/1289
dc.identifier.uri doi:10.1007/s12031-010-9395-0
dc.description.abstract The primary sensory neurons use glutamate as a major neurotransmitter. Several neuropeptides are also found in these neurons. In our laboratory we demonstrated secretin-like immunoreactivity in primary sensory neurons of several species including human, rat and cat. In the present experiment utilizing in situ hybridization, we have demonstrated for the first time that secretin is not only immunostained but is also expressed in the primary sensory neurons of the trigeminal ganglion of male rats. In intact rats, secretin mRNA was not observed; we had to use intracerebroventricular colchicine administration to induce the expression of secretin. Secretin was expressed in about 5% of the cells in all the three subdivisions of the trigeminal ganglion. The secretin- synthetizing cells were large and medium sized, and their mean diameter was about 50 mum. When we compared the percentage and the size of secretin to that of calcitonin gene-related peptide (CGRP), substance-P (SP) and vasoactive intestinal polypeptide (VIP) cells, it was found that CGRP, SP and VIP are present in about 15-20% of the cells and their mean diameter is about 20- 25 mum. The morphometric data indicate that secretin is present in a subdivision of neurons that is different from the subdivision of the CGRP, SP and VIP cells. It is suggested that secretin may modulate the function of the primary neurotransmitter.
dc.relation.ispartof urn:issn:0895-8696
dc.title Secretin mRNA in the subdivision of primary sensory neurons in the trigeminal ganglion of rats.
dc.type Journal Article
dc.date.updated 2015-02-02T11:54:03Z
dc.language.rfc3066 en
dc.identifier.mtmt 1460954
dc.identifier.wos 000286106100015
dc.identifier.pubmed 20582488
dc.contributor.department MTA TKI/MTA-SE Neuromorfológiai és Neuroendokrin Kutatócsoport (2006-ig: MTA-SE Neuroendokrin Kutatócsoport)
dc.contributor.department SE/AOK/I/Anatómiai, Szövet- és Fejlődéstani Intézet
dc.contributor.department SE/AOK/I/Humánmorfológiai és Fejlődésbiológiai Intézet
dc.contributor.institution MTA Támogatott Kutatócsoportok
dc.contributor.institution Semmelweis Egyetem


Kapcsolódó fájlok:

A fájl jelenleg csak egyetemi IP címről érhető el.

Megtekintés/Megnyitás

Ez a rekord az alábbi gyűjteményekben szerepel:

Egyszerű nézet