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呋塞米对畸变产物耳声发射及耳蜗腹侧前核神经元反应的影响。

Effects of furosemide on distortion product otoacoustic emissions and on neuronal responses in the anteroventral cochlear nucleus.

作者信息

Rübsamen R, Mills D M, Rubel E W

机构信息

Virginia Merrill Bloedel Hearing Research Center, University of Washington, Seattle 98195, USA.

出版信息

J Neurophysiol. 1995 Oct;74(4):1628-38. doi: 10.1152/jn.1995.74.4.1628.

Abstract
  1. The objective of this study was to precisely evaluate the relationship between the threshold of neurons in the anteroventral cochlear nucleus (AVCN) and the properties of distortion product otoacoustic emissions (DPOAEs). Response areas of multiunit clusters in the AVCN and DPOAEs in the ear canal were measured alternately in the adult gerbil during furosemide-induced changes of the endocochlear potential. Stimulus frequencies of the probe tones for DPOAE measurement were in the range of f1 = 1.7-7.6 kHz and f2 = 2.0-9.0 kHz; the ratio f2:f1 was always 1.18. Stimulus amplitudes were varied in 5-dB steps from 30 to 80 dB SPL, with either equal amplitudes (L1 = L2) or unequal, with L1 set 10 dB above L2. Multiunit response areas were determined from cluster responses to a series of 100-ms tone bursts presented with a pseudo-random sequence in frequency and intensity. 2. Changes in the multiunit discharge properties after 50-75 mg/kg furosemide injection were as follows: the best frequency (BF) threshold increased from initial values in the range of 20-30 dB SPL to 50-80 dB SPL at 10-20 min postinjection and then recovered fully by 60-90 min. The spontaneous discharge activity decreased to zero before any changes in the frequency threshold curve were observed and did not return to initial values for several hours. Likewise, total discharge rates of stimulus elicited responses were reduced and tended to stay reduced even after BF threshold had fully recovered. 3. From the DPOAE measurements, the changes observed in the cubic distortion tone (CDT, 2f1-f2) emission after furosemide injection were as follows: at high levels of the probe tones, changes in the emission intensities generally stayed within a 10-dB range. The CDT amplitudes for low stimulus levels, however, were typically reduced by up to 40 dB, but recovered (depending on the furosemide dosage) by approximately 60-90 min. 4. At low to moderate stimulus levels of 40-60 dB SPL, there was a near perfect, minute-by-minute covariation of the ear canal CDT amplitude and the BF threshold measured in the AVCN. A 10-dB increase in threshold was associated with a 5- to 7-dB decrease in the CDT emission. 5. The optimum stimulus parameter set for the noninvasive estimation of cochlear performance from the CDT response was for stimulus amplitudes L1 = 50, L2 = 40 dB SPL. 6. This experiment demonstrates that CDT emissions at low stimulus levels are very good predictors of the thresholds of cochlear afferents, but this validity is lost for BF thresholds greater than approximately 60-70 dB SPL. 7. The ear canal CDT amplitude is better correlated with the BF threshold sensitivity of neuronal response areas in the AVCN than with the spontaneous discharge rate or absolute above-threshold discharge rates.
摘要
  1. 本研究的目的是精确评估耳蜗前腹侧核(AVCN)中神经元的阈值与畸变产物耳声发射(DPOAE)特性之间的关系。在成年沙鼠中,通过速尿诱导的内淋巴电位变化期间,交替测量AVCN中多单元簇的反应区域和耳道中的DPOAE。用于DPOAE测量的探测音的刺激频率范围为f1 = 1.7 - 7.6 kHz和f2 = 2.0 - 9.0 kHz;f2:f1的比值始终为1.18。刺激幅度以5 dB步长从30 dB SPL变化到80 dB SPL,要么幅度相等(L1 = L2),要么不相等,L1设置为比L2高10 dB。多单元反应区域通过对一系列以频率和强度的伪随机序列呈现的100 ms短音爆的簇反应来确定。2. 注射50 - 75 mg/kg速尿后多单元放电特性的变化如下:最佳频率(BF)阈值从注射后10 - 20分钟时的初始值20 - 30 dB SPL增加到50 - 80 dB SPL,然后在60 - 90分钟时完全恢复。在频率阈值曲线出现任何变化之前,自发放电活动降至零,并且在数小时内未恢复到初始值。同样,刺激诱发反应的总放电率降低,并且即使在BF阈值完全恢复后仍倾向于保持降低。3. 从DPOAE测量中,速尿注射后观察到的立方畸变音(CDT,2f1 - f2)发射的变化如下:在探测音的高水平时,发射强度的变化通常保持在10 dB范围内。然而,低刺激水平下的CDT幅度通常降低多达40 dB,但(取决于速尿剂量)在大约60 - 90分钟时恢复。4. 在40 - 60 dB SPL的低至中等刺激水平下,耳道CDT幅度与在AVCN中测量的BF阈值之间存在近乎完美的逐分钟协变。阈值增加10 dB与CDT发射降低5至7 dB相关。5. 用于从CDT反应无创估计耳蜗性能的最佳刺激参数设置为刺激幅度L1 = 50,L2 = 40 dB SPL。6. 本实验表明,低刺激水平下的CDT发射是耳蜗传入神经阈值的良好预测指标,但对于大于约60 - 70 dB SPL的BF阈值,这种有效性丧失。7. 耳道CDT幅度与AVCN中神经元反应区域的BF阈值敏感性的相关性比与自发放电率或绝对阈上放电率的相关性更好。

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