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The VR1-Positive primary afferent-mediated expression of pERK in the lumbosacral neurons in response to mechanical and chemical stimulation of the urinary bladder in ratsopen access

Authors
Yoo, Chan JongHwang, Se Jin
Issue Date
Dec-2007
Publisher
KOREAN NEUROSURGICAL SOC
Keywords
spinal cord; visceral sense; primary afferent; pERK; NK1; VR1
Citation
JOURNAL OF KOREAN NEUROSURGICAL SOCIETY, v.42, no.6, pp.462 - 469
Indexed
SCIE
KCI
Journal Title
JOURNAL OF KOREAN NEUROSURGICAL SOCIETY
Volume
42
Number
6
Start Page
462
End Page
469
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/179263
DOI
10.3340/jkns.2007.42.6.462
ISSN
2005-3711
Abstract
Objective : This study characterized the neurons in the lumbosacral cord that express phospho ERK (pERK) after distension or irritation of the bladder, and their relation to the vanilloid receptor 1 (VR1) positive primary afferents. Methods : Mechanical distension and chemical irritation of the bladder were induced by intravesical injection of the saline and mustard oil, respectively. Spinal neurons expressing pERK and the primary afferent fibers were characterized using multiple immunofluorescence for neurokinin 1 (NK1), neuronal nitric oxide synthetase (nNOS) and VR1. Results: Neurons in lamina 1, medial dorsal horn (MDH), dorsal gray commissure (DGC) and sacral parasympathetic nucleus (SPN) were immunoreactive for pERK after either mechanical or chemical stimulation. The majority of pERK positive cells were positive for NK1 in lamina I and SPN, but not in the DGC. Most of pERK positive cells are not stained for nNOS except in a small population of the cells in the SPN and DGC. Contacts between perikarya and dendrites of pERK-positive cells and terminals of primary afferents expressing VRI were identified in lamina 1, lateral collateral path (LCP) and SPN. Conclusion : In this study, the lumbosacral neurons activated by mechanical and chemical stimulation of the urinary bladder were identified with expression of the pERK, and also provided the evidence that VR1-positive primary afferents may mediate the activation of these neurons.
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