EFFECT OF OTOTOXICITY ON AUDITORY EVOKED POTENTIALS
EFFECT OF OTOTOXICITY ON AUDITORY EVOKED POTENTIALS
批准号:
3080298
负责人:
KATHLEEN CAMPBELL
金额:
$8.71万
依托单位国家:
美国
项目类别:
财政年份:
1990
资助国家:
美国
项目状态:
已结题
起止时间:
1990-04-01 至 1995-03-31
关键词:
acoustic nerve audiometry auditory discrimination auditory pathways auditory threshold chinchilla cochlea conductive hearing loss diagnosis design /evaluation drug adverse effect ear disorder chemotherapy ear pharmacology electronic recording system electrophysiology evoked potentials furosemide gentamicins histology human subject noninvasive diagnosis ototoxin scanning electron microscopy
中文摘要
拟议研究的重点是检查急性和慢性影响。
耳毒性制剂对耳蜗电生理活动的影响,
经无创耳蜗术(ECOG)检查的神经、脑干
和听性脑干反应(ABR)。其主要目的是
确定是否可以使用ECOG或ABR的变化来预测即将发生的情况
听力损失或在听力损失发生之前提供听力损失的早期识别
不可逆转。如果这些措施确实提供了这样的指标,那么其有效性
病人护理的质量可能会得到加强。实验将从以下方面开始
经鼓室无创脑电记录技术的研究进展
后续手术所需的龙猫耳膜(TM)和耳道
耳毒性的慢性动物研究。同步记录非侵入性
和侵入性测量总和电位(SP)的幅度、动作
然后,潜在(AP)幅度、AP延迟和AP阈值
比较一下。无创脑电地形图记录技术在这些地区的发展
动物将不再需要手术,特别是重复手术
,在五月份由我们和其他人进行的动物研究。因此,需要
用于术后镇痛剂和抗生素以及无菌手术室
可以显著减少动物在慢性疾病中的痛苦
实验。然后,非侵入性记录技术在
动物和以前开发的无创记录技术
成年人的TM将被用来检查耳毒性的慢性影响
药物对SP波幅、AP波幅、SP/AP波幅比、AP的影响
延迟强度函数、AP输入输出函数、AP和ABR
听性脑干的阈值和适应与I-V间期
回应。在人类成年人中,行为测听阈值也将
被监视。在动物身上,将进行耳蜗学的组织学研究
在牺牲之后。在第三年,我们计划将动物研究扩大到
包括耳毒性和频率选择性单一单元研究
以单单元记录、ECOG记录或两者兼而有之。此外,
我们计划扩大无创耳蜗术的发展
对婴幼儿和新生儿的技术。婴幼儿和新生儿接受
然后可以包括耳毒性药物进行研究。在整个赠款过程中
在此期间,私家侦探将学习化学、药理学和
电子显微镜。同时,她将教书和督导
耳鼻咽喉科住院医师、医学生和药理学博士
学生在脑干听觉诱发电位、ABR和耳毒性方面。
英文摘要
The focus of the proposed study is to examine the acute and chronic effects
of ototoxic preparations on the electrophysiologic activity of the cochlea,
VIII nerve, and brainstem through noninvasive electrocochleography (ECOG)
and the auditory brainstem response (ABR). The primary purpose is to
determine if changes in the ECOG or ABR can be used to predict impending
hearing loss or provide early identification of a hearing loss before it is
irreversible. If these measures do provide such an indicant, the efficacy
of patient care may be enhanced. Experiments will begin with the
development of noninvasive ECOG recording techniques from the tympanic
membrane (TM) and ear canal of chinchillas needed for the subsequent
chronic animal study of ototoxicity. Simultaneously recorded noninvasive
and invasive measures of the summating potential (SP) amplitude, action
potential (AP) amplitude, AP latency, and AP threshold will then be
compared. Development of noninvasive ECOG recording techniques in these
animals will eliminate the need for surgery, particularly repeated surgery
, in may animal studies by ourselves and others. Consequently, the need
for postoperative analgesics and antibiotics and sterile operating rooms
could be markedly curtailed as well as possible animal suffering in chronic
experiments. Then the noninvasive recording techniques developed in
animals and previously developed noninvasive recording techniques from the
TM in adult humans will be used to examine the chronic effects of ototoxic
agents on SP amplitude, AP amplitude, the SP/AP amplitude ratio, AP
latency-intensity functions, AP input-output functions, AP and ABR
threshold and adaptation and the I-V interval of the auditory brainstem
response. In the human adults, behavioral audiometric thresholds will also
be monitored. In the animals, histology of the cochlea will be performed
after sacrifice. In the third year, we plan to expand animal studies to
include single unit studies of ototoxicity, and frequency selectivity
either in single unit recordings, ECOG recordings, or both. In addition,
we plan to expand the development of noninvasive electrocochleographic
techniques to infants and neonates. Infants and neonates receiving
ototoxic agents could then be included for study. Throughout the grant
period the P.I. will take formal coursework in chemistry, pharmacology, and
electron microscopy. Simultaneously, she will teach and supervise
otolaryngology residents, medical students, and pharmacology doctoral
students in the area of ECOG, ABR, and ototoxicity.
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