Type 1 vanilloid receptor expression by mammalian inner ear ganglion cells

被引:47
作者
Balaban, CD
Zhou, JX
Li, HS
机构
[1] Univ Pittsburgh, Sch Med, Dept Otolaryngol, Inst Eye & Ear, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Sch Med, Dept Neurobiol, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Sch Med, Dept Commun Sci & Disorders, Pittsburgh, PA 15213 USA
关键词
D O I
10.1016/S0378-5955(02)00734-7
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
The type I vanilloid receptor (VR1) is a non-specific cation channel activated by capsaicin, lipoxygenase (LOX) products, heat and acid. This study demonstrates VR1 and 5-LOX expression by inner ear ganglion cells. A PCR product (210 bp) was amplified from both oligo(dT)- and random primer-generated cDNAs of rat spiral ganglion cells using VR1 gene-specific primers constructed from the 3' non-homologous region. This PCR product shared 100% sequence homology to a rat VR1 cDNA (GenBank accession no. AF029310) and a rat vanilloid receptor splice variant mRNA (GenBank accession no. AF158248). Frozen sections of PLP-fixed, decalcified Long-Evans rat temporal bones were stained immunohistochemically for VR1 Neurons and satellite cells in both the vestibular and spiral ganglia were VR1-immunopositive. Neurons and supporting cells in adjacent sections of these ganglia were immunopositive for 5-LOX. These findings raise the hypothesis that activation of VR1 by endogenous ligands may contribute to hypersensitivity of the eighth nerve to hair cell inputs in a variety of pathologic conditions, such Lis tinnitus, Meniere's disease and migraine. In particular, these data suggest that LOX activation during inflammatory processes or during cyclo-oxygenase inhibition (e.g. by aspirin) is a potential intrinsic source of VR1 activation in inner ear ganglia. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:165 / 170
页数:6
相关论文
共 11 条
[1]   Impaired nociception and pain sensation in mice lacking the capsaicin receptor [J].
Caterina, MJ ;
Leffler, A ;
Malmberg, AB ;
Martin, WJ ;
Trafton, J ;
Petersen-Zeitz, KR ;
Koltzenburg, M ;
Basbaum, AI ;
Julius, D .
SCIENCE, 2000, 288 (5464) :306-313
[2]   The capsaicin receptor: a heat-activated ion channel in the pain pathway [J].
Caterina, MJ ;
Schumacher, MA ;
Tominaga, M ;
Rosen, TA ;
Levine, JD ;
Julius, D .
NATURE, 1997, 389 (6653) :816-824
[3]   Opioids, NSAIDs and 5-lipoxygenase inhibitors act synergistically in brain via arachidonic acid metabolism [J].
Christie, MJ ;
Vaughan, CW ;
Ingram, SL .
INFLAMMATION RESEARCH, 1999, 48 (01) :1-4
[4]  
Fosslien E, 1998, ANN CLIN LAB SCI, V28, P67
[5]   Direct activation of capsaicin receptors by products of lipoxygenases: Endogenous capsaicin-like substances [J].
Hwang, SW ;
Cho, H ;
Kwak, J ;
Lee, SY ;
Kang, CJ ;
Jung, J ;
Cho, S ;
Min, KH ;
Suh, YG ;
Kim, D ;
Oh, U .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :6155-6160
[6]   Acid potentiation of the capsaicin receptor determined by a key extracellular site [J].
Jordt, SE ;
Tominaga, M ;
Julius, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (14) :8134-8139
[7]  
Jung J, 1999, J NEUROSCI, V19, P529
[8]   PERIODATE-LYSINE-PARAFORMALDEHYDE FIXATIVE - NEW FIXATIVE FOR IMMUNOELECTRON MICROSCOPY [J].
MCLEAN, IW ;
NAKANE, PK .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1974, 22 (12) :1077-1083
[9]  
RASKMADSEN J, 1992, AGENTS ACTIONS, pC36
[10]   Molecular cloning of an N-terminal splice variant of the capsaicin receptor - Loss of N-terminal domain suggests functional divergence among capsaicin receptor subtypes [J].
Schumacher, MA ;
Moff, I ;
Sudanagunta, SP ;
Levine, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (04) :2756-2762