Neural changes accompanying tinnitus following unilateral acoustic trauma in the guinea pig

被引:71
作者
Coomber, Ben [1 ]
Berger, Joel I. [1 ]
Kowalkowski, Victoria L. [1 ]
Shackleton, Trevor M. [1 ]
Palmer, Alan R. [1 ]
Wallace, Mark N. [1 ]
机构
[1] MRC Inst Hearing Res, Nottingham NG7 2RD, England
关键词
auditory; behaviour; electrophysiology; inferior colliculus; nitric oxide synthase; NITRIC-OXIDE SYNTHASE; LONG-TERM POTENTIATION; VENTRAL COCHLEAR NUCLEUS; AUDITORY BRAIN-STEM; INTENSE SOUND EXPOSURE; NEURONAL NADPH DIAPHORASE; INDUCED HEARING-LOSS; DORSAL-ROOT GANGLIA; INFERIOR COLLICULUS; NEUROPATHIC PAIN;
D O I
10.1111/ejn.12580
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Animal models of tinnitus allow us to study the relationship between changes in neural activity and the tinnitus percept. Here, guinea pigs were subjected to unilateral noise trauma and tested behaviourally for tinnitus 8 weeks later. By comparing animals with tinnitus with those without, all of which were noise-exposed, we were able to identify changes unique to the tinnitus group. Three physiological markers known to change following noise exposure were examined: spontaneous firing rates (SFRs) and burst firing in the inferior colliculus (IC), evoked auditory brainstem responses (ABRs), and the number of neurons in the cochlear nucleus containing nitric oxide synthase (NOS). We obtained behavioural evidence of tinnitus in 12 of 16 (75%) animals. Both SFRs and incidences of burst firing were elevated in the IC of all noise-exposed animals, but there were no differences between tinnitus and no-tinnitus animals. There were significant decreases in ipsilateral ABR latencies in tinnitus animals, contrary to what might be expected with a small hearing loss. Furthermore, there was an ipsilateral-contralateral asymmetry in NOS staining in the ventral cochlear nucleus (VCN) that was only apparent in tinnitus animals. Tinnitus animals had a significantly greater number of NOS-containing neurons on the noise-exposed side, whereas no-tinnitus animals did not. These data suggest that measuring NOS in the VCN and recording ABRs supplement behavioural methods for confirming tinnitus in animals, and that nitric oxide is involved in plastic neural changes associated with tinnitus.
引用
收藏
页码:2427 / 2441
页数:15
相关论文
共 111 条
[1]   Assessing tinnitus and prospective tinnitus therapeutics using a psychophysical animal model [J].
Bauer, CA ;
Brozoski, TJ .
JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY, 2001, 2 (01) :54-64
[2]   Tinnitus and inferior colliculus activity in chinchillas related to three distinct patterns of cochlear trauma [J].
Bauer, Carol A. ;
Turner, Jeremy G. ;
Caspary, Donald M. ;
Myers, Kristin S. ;
Brozoski, Thomas J. .
JOURNAL OF NEUROSCIENCE RESEARCH, 2008, 86 (11) :2564-2578
[3]   Primary afferent dendrite degeneration as a cause of tinnitus [J].
Bauer, Carol A. ;
Brozoski, Thomas J. ;
Myers, Kristin .
JOURNAL OF NEUROSCIENCE RESEARCH, 2007, 85 (07) :1489-1498
[4]   A novel behavioural approach to detecting tinnitus in the guinea pig [J].
Berger, Joel I. ;
Coomber, Ben ;
Shackleton, Trevor M. ;
Palmer, Alan R. ;
Wallace, Mark N. .
JOURNAL OF NEUROSCIENCE METHODS, 2013, 213 (02) :188-195
[5]   New growth of axons in the cochlear nucleus of adult chinchillas after acoustic trauma [J].
Bilak, M ;
Kim, J ;
Potashner, SJ ;
Bohne, BA ;
Morest, DK .
EXPERIMENTAL NEUROLOGY, 1997, 147 (02) :256-268
[6]   MODULATION OF MORPHINE ANTINOCICEPTION IN THE MOUSE BY ENDOGENOUS NITRIC-OXIDE [J].
BRIGNOLA, G ;
CALIGNANO, A ;
DIROSA, M .
BRITISH JOURNAL OF PHARMACOLOGY, 1994, 113 (04) :1372-1376
[7]   Elevated fusiform cell activity in the dorsal cochlear nucleus of chinchillas with psychophysical evidence of tinnitus [J].
Brozoski, TJ ;
Bauer, CA ;
Caspary, DM .
JOURNAL OF NEUROSCIENCE, 2002, 22 (06) :2383-2390
[8]   FAR-FIELD ACOUSTIC RESPONSE - ORIGINS IN CAT [J].
BUCHWALD, JS ;
HUANG, CM .
SCIENCE, 1975, 189 (4200) :382-384
[9]   COMPACT AND EASY-TO-USE TUNGSTEN-IN-GLASS MICROELECTRODE MANUFACTURING WORKSTATION [J].
BULLOCK, DC ;
PALMER, AR ;
REES, A .
MEDICAL & BIOLOGICAL ENGINEERING & COMPUTING, 1988, 26 (06) :669-672
[10]  
Burette A, 2001, J COMP NEUROL, V431, P1, DOI 10.1002/1096-9861(20010226)431:1<1::AID-CNE1051>3.0.CO