Distribution of gastrin‐releasing peptide in the rat trigeminal and spinal somatosensory systems. Issue 8 (1st June 2014)
- Record Type:
- Journal Article
- Title:
- Distribution of gastrin‐releasing peptide in the rat trigeminal and spinal somatosensory systems. Issue 8 (1st June 2014)
- Main Title:
- Distribution of gastrin‐releasing peptide in the rat trigeminal and spinal somatosensory systems
- Authors:
- Takanami, Keiko
Sakamoto, Hirotaka
Matsuda, Ken Ichi
Satoh, Keita
Tanida, Takashi
Yamada, Shunji
Inoue, Kaihei
Oti, Takumi
Sakamoto, Tatsuya
Kawata, Mitsuhiro - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>Gastrin‐releasing peptide (GRP) has recently been identified as an itch‐specific neuropeptide in the spinal sensory system in mice, but there are no reports of the expression and distribution of GRP in the trigeminal sensory system in mammals. We characterized and compared GRP‐immunoreactive (ir) neurons in the trigeminal ganglion (TG) with those in the rat spinal dorsal root ganglion (DRG). GRP immunoreactivity was expressed in 12% of TG and 6% of DRG neurons and was restricted to the small‐ and medium‐sized type cells. In both the TG and DRG, many GRP‐ir neurons also expressed substance P and calcitonin gene‐related peptide, but not isolectin B<sub>4</sub>. The different proportions of GRP and transient receptor potential vanilloid 1 double‐positive neurons in the TG and DRG imply that itch sensations via the TG and DRG pathways are transmitted through distinct mechanisms. The distribution of the axon terminals of GRP‐ir primary afferents and their synaptic connectivity with the rat trigeminal sensory nuclei and spinal dorsal horn were investigated by using light and electron microscopic histochemistry. Although GRP‐ir fibers were rarely observed in the trigeminal sensory nucleus principalis, oralis, and interpolaris, they were predominant in the superficial layers of the trigeminal sensory nucleus caudalis (Vc), similar to the spinal dorsal horn. Ultrastructural analysis revealed that GRP‐ir terminals contained<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Gastrin‐releasing peptide (GRP) has recently been identified as an itch‐specific neuropeptide in the spinal sensory system in mice, but there are no reports of the expression and distribution of GRP in the trigeminal sensory system in mammals. We characterized and compared GRP‐immunoreactive (ir) neurons in the trigeminal ganglion (TG) with those in the rat spinal dorsal root ganglion (DRG). GRP immunoreactivity was expressed in 12% of TG and 6% of DRG neurons and was restricted to the small‐ and medium‐sized type cells. In both the TG and DRG, many GRP‐ir neurons also expressed substance P and calcitonin gene‐related peptide, but not isolectin B<sub>4</sub>. The different proportions of GRP and transient receptor potential vanilloid 1 double‐positive neurons in the TG and DRG imply that itch sensations via the TG and DRG pathways are transmitted through distinct mechanisms. The distribution of the axon terminals of GRP‐ir primary afferents and their synaptic connectivity with the rat trigeminal sensory nuclei and spinal dorsal horn were investigated by using light and electron microscopic histochemistry. Although GRP‐ir fibers were rarely observed in the trigeminal sensory nucleus principalis, oralis, and interpolaris, they were predominant in the superficial layers of the trigeminal sensory nucleus caudalis (Vc), similar to the spinal dorsal horn. Ultrastructural analysis revealed that GRP‐ir terminals contained clear microvesicles and large dense‐cored vesicles, and formed asymmetric synaptic contacts with a few dendrites in the Vc and spinal dorsal horn. These results suggest that GRP‐dependent orofacial and spinal pruriceptive inputs are processed mainly in the superficial laminae of the Vc and spinal dorsal horn. J. Comp. Neurol. 522:1858–1873, 2014. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Journal of comparative neurology. Volume 522:Issue 8(2014:Jun. 01)
- Journal:
- Journal of comparative neurology
- Issue:
- Volume 522:Issue 8(2014:Jun. 01)
- Issue Display:
- Volume 522, Issue 8 (2014)
- Year:
- 2014
- Volume:
- 522
- Issue:
- 8
- Issue Sort Value:
- 2014-0522-0008-0000
- Page Start:
- 1858
- Page End:
- 1873
- Publication Date:
- 2014-06-01
- Subjects:
- Comparative neurobiology -- Periodicals
Neurology -- Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1096-9861 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cne.23506 ↗
- Languages:
- English
- ISSNs:
- 0021-9967
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4962.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3307.xml