Melcher J R, Knudson I M, Fullerton B C, Guinan J J, Norris B E, Kiang N Y
Massachusetts Eye and Ear Infirmary, Boston 02114, USA.
Hear Res. 1996 Apr;93(1-2):1-27. doi: 10.1016/0378-5955(95)00178-6.
This paper is the first in a series aimed at identifying the cellular generators of the brainstem auditory evoked potential (BAEP) in cats. The approach involves (1) developing experimental procedures for making small selective lesions and determining the corresponding changes in BAEP waveforms, (2) identifying brainstem regions involved in BAEP generation by examining the effects of lesions on the BAEP and (3) identifying specific cell populations involved by combining the lesion results with electrophysiological and anatomical information from other kinds of studies. We created lesions in the lower brainstem by injecting kainic acid which is generally toxic for neuronal cell bodies but not for axons and terminals. This first paper describes the justifications for using kainic acid, explains the associated problems, and develops a methodology that addresses the main difficulties. The issues and aspects of the specific methods are generally applicable to physiological and anatomical studies using any neurotoxin, as well as to the present BAEP study. The methods chosen involved (1) measuring the BAEP at regular intervals until it reached a post-injection steady state and perfusing the animals with fixative shortly after the last BAEP recordings were made, (2) using objective criteria to distinguish injection-related BAEP changes from unrelated ones, (3) making control injections to identify effects not due to kainic acid toxicity, (4) verifying the anatomical and functional integrity of axons in lesioned regions, and (5) examining injected brainstems microscopically for cell loss and cellular abnormalities indicating dysfunction. This combination of methods enabled us to identify BAEP changes which are clearly correlated with lesion locations.
本文是系列论文中的第一篇,旨在确定猫脑干听觉诱发电位(BAEP)的细胞起源。该方法包括:(1)开发用于制造小范围选择性损伤并确定BAEP波形相应变化的实验程序;(2)通过检查损伤对BAEP的影响来确定参与BAEP产生的脑干区域;(3)将损伤结果与其他类型研究的电生理和解剖学信息相结合,以确定具体涉及的细胞群。我们通过注射 kainic 酸在脑桥下部制造损伤,kainic 酸一般对神经元细胞体有毒性,但对轴突和终末无毒性。第一篇论文阐述了使用 kainic 酸的理由,解释了相关问题,并开发了一种解决主要困难的方法。特定方法的问题和方面通常适用于使用任何神经毒素的生理和解剖学研究,以及当前的BAEP研究。所选用的方法包括:(1)定期测量BAEP,直至其达到注射后的稳定状态,并在最后一次BAEP记录后不久用固定剂灌注动物;(2)使用客观标准区分与注射相关的BAEP变化和无关变化;(3)进行对照注射以确定非kainic酸毒性引起的效应;(4)验证损伤区域轴突的解剖和功能完整性;(5)在显微镜下检查注射后的脑干,观察细胞丢失和表明功能障碍的细胞异常情况。这种方法组合使我们能够识别与损伤位置明显相关的BAEP变化。