Miller Charles A, Abbas Paul J, Hay-McCutcheon Marcia J, Robinson Barbara K, Nourski Kirill V, Jeng Fuh-Cherng
Department of Otolaryngology, Head and Neck Surgery, University of Iowa Hospitals and Clinics, 21201 PFP, 200 Hawkins Drive, Iowa City, IA 52242, USA.
Hear Res. 2004 Dec;198(1-2):75-86. doi: 10.1016/j.heares.2004.07.005.
With experimental animals, the electrically evoked compound action potential (ECAP) can be recorded from multiple sites (e.g., round window, intracranial and intracochlear sites). However, human ECAPs are typically recorded from intracochlear electrodes of the implanted array. To bridge this difference, we obtained ECAPs from cats using both intracochlear and nerve-trunk recording sites. We also sought to determine how recording the site influences the acquired evoked potential and how those differences may provide insight into basic excitation properties. In the main experiment, ECAPs were recorded from four acutely deafened cats after implanting a Nucleus-style banded electrode array. Potentials were recorded from an electrode positioned on the nerve trunk and an intracochlear electrode. We manipulated stimulus level, electrode configuration (monopolar vs bipolar) and stimulus polarity, variables that influence the site of excitation. Intracochlear ECAPs were found to be an order of magnitude greater than those obtained with the nerve-trunk electrode. Also, compared with the nerve-trunk potentials, the intracochlear ECAPs more closely resembled those obtained from humans in that latencies were shorter and the waveform morphology was typically biphasic (a negative peak followed by a positive peak). With anodic monophasic stimuli, the ECAP had a unique positive-to-negative morphology which we attributed to antidromic action potentials resulting from a relatively central site of excitation. We also collected intracochlear ECAPs from twenty Nucleus 24 implant users. Compared with the feline ECAPs, the human potentials had smaller amplitudes and longer latencies. It is not clear what underlies these differences, although several factors are considered.
对于实验动物,可以从多个部位(如圆窗、颅内和耳蜗内部位)记录电诱发复合动作电位(ECAP)。然而,人类的ECAP通常是从植入阵列的耳蜗内电极记录的。为了弥合这种差异,我们使用耳蜗内和神经干记录部位从猫身上获取了ECAP。我们还试图确定记录部位如何影响所获得的诱发电位,以及这些差异如何有助于深入了解基本的兴奋特性。在主要实验中,在植入Nucleus式带状电极阵列后,从四只急性致聋的猫身上记录ECAP。从位于神经干上的电极和耳蜗内电极记录电位。我们操纵了刺激水平、电极配置(单极与双极)和刺激极性等影响兴奋部位的变量。发现耳蜗内ECAP比从神经干电极获得的电位大一个数量级。此外,与神经干电位相比,耳蜗内ECAP更类似于从人类获得的电位,因为其潜伏期更短,波形形态通常为双相(一个负峰后接一个正峰)。对于阳极单相刺激,ECAP具有独特的正到负形态,我们将其归因于相对中央兴奋部位产生的逆向动作电位。我们还从20名使用Nucleus 24植入物的用户身上收集了耳蜗内ECAP。与猫的ECAP相比,人类的电位幅度更小,潜伏期更长。尽管考虑了几个因素,但尚不清楚这些差异的根本原因。