Expression of inducible nitric oxide synthase (iNOS/NOS II) in the cochlea of guinea pigs after intratympanical endotoxin-treatment

被引:76
作者
Hess, A
Bloch, W
Huverstuhl, J
Su, JP
Stennert, E
Addicks, K
Michel, O
机构
[1] Univ Cologne, Klin & Poliklin Hals Nasen & Ohrenheilkunde, Dept Oto Rhino Laryngol, D-50924 Cologne, Germany
[2] Univ Cologne, Dept Anat, D-50924 Cologne, Germany
关键词
nitric oxide; iNOS; soluble guanylyl cyclase; cochlea; inner ear dysfunction;
D O I
10.1016/S0006-8993(99)01433-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Since NO is believed to be involved in cochlear physiology, presence of the constitutive isoforms of nitric oxide synthase (NOS), and the target enzyme of NO, soluble guanylyl cyclase (sGC) in structures of the mammalian cochlea have been demonstrated. To date, no reports have been published regarding the detection of the inducible isoform (NOS II) in the cochlea. In order to show the capability of iNOS expression in cochlear tissue, a mixture of proinflammatory bacterial lipopolysaccharides (LPS) and tumor necrosis factor a (TNF-alpha) was injected into the tympanic cavity of guinea pigs, vs. saline-solution as control. Paraffin sections of LPS/TNF-alpha treated and saline-treated cochleae (6 h) were examined immunohistochemically with specific antibodies to neuronal, endothelial and inducible NOS and to sGC. Initiated expression of iNOS in the cochlea was observed in the wall of blood vessels of the spiral ligament (SL) and the modiolus, in supporting cells of the organ of Corti, in the limbus, in nerve fibers and in a part of the perikarya of the spiral ganglion after LPS/TNF alpha-treatment. iNOS was not detected in saline-treated control tissue. Expression of both constitutive NOS-isoforms (endothelial and neuronal NOS) and of sGC showed no significant differences in both experimental groups. Endothelial eNOS and neuronal bNOS were detected co-localized in ganglion cells, in nerve fibers, in cells of the SL and in supporting cells of the organ of Corti, but not in sensory cells. Strong labeling for bNOS became evident in the endosteum of the cochlea, while in the endothelium of blood vessels and in the epithelium of the limbus only eNOS could be labeled, sGC could be detected in SL, in supporting and sensory cells of the organ of Corti, in nerve fibers, ganglion cells, in the wall of blood vessels and in the limbus-epithelium. While small amounts of NO, generated by bNOS and eNOS, seem to support the cochlear blood flow and auditory function as well. as neurotransmission, high amounts of iNOS-generated NO could have dysregulative and neurotoxic effects on the inner ear during bacterial and viral infections of the middle and inner ear. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:113 / 122
页数:10
相关论文
共 50 条
[1]   NO synthase-II is transiently expressed in embryonic mouse olfactory receptor neurons [J].
Arnhold, S ;
Andressen, C ;
Bloch, W ;
Mai, JK ;
Addicks, K .
NEUROSCIENCE LETTERS, 1997, 229 (03) :165-168
[2]   Nitric oxide: A mediator of endotoxin-induced middle ear effusions [J].
Ball, SS ;
Prazma, J ;
Dais, CGD ;
Rosbe, KW ;
Pillsbury, HC .
LARYNGOSCOPE, 1996, 106 (08) :1021-1027
[3]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[4]  
BLOCH W, 1995, AGENT ACTION SUPPL, V45, P151
[5]   BASAL NITRIC-OXIDE PRODUCTION IN REGULATION OF COCHLEAR BLOOD-FLOW [J].
BRECHTELSBAUER, PB ;
NUTTALL, AL ;
MILLER, JM .
HEARING RESEARCH, 1994, 77 (1-2) :38-42
[6]   NITRIC-OXIDE PRODUCED BY ACTIVATED ASTROCYTES RAPIDLY AND REVERSIBLY INHIBITS CELLULAR RESPIRATION [J].
BROWN, GC ;
BOLANOS, JP ;
HEALES, SJR ;
CLARK, JB .
NEUROSCIENCE LETTERS, 1995, 193 (03) :201-204
[7]  
Chole RA, 1998, ACTA OTO-LARYNGOL, V118, P705
[8]  
CHOW JWM, 1996, J BONE MINER RES S1, V11, pS270
[9]   REVERSIBLE INHIBITION OF CYTOCHROME-C-OXIDASE, THE TERMINAL ENZYME OF THE MITOCHONDRIAL RESPIRATORY-CHAIN, BY NITRIC-OXIDE - IMPLICATIONS FOR NEURODEGENERATIVE DISEASES [J].
CLEETER, MWJ ;
COOPER, JM ;
DARLEYUSMAR, VM ;
MONCADA, S ;
SCHAPIRA, AHV .
FEBS LETTERS, 1994, 345 (01) :50-54
[10]  
CUNHA FQ, 1994, IMMUNOLOGY, V81, P211