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本文引用的文献

1
The frequency selectivity of auditory nerve fibres and hair cells in the cochlea of the turtle.乌龟耳蜗中听觉神经纤维和毛细胞的频率选择性。
J Physiol. 1980 Sep;306:79-125. doi: 10.1113/jphysiol.1980.sp013387.
2
Hair cells and tectorial membrane in the cochlea of the greater horseshoe bat.大马蹄蝠耳蜗中的毛细胞和盖膜。
Anat Embryol (Berl). 1980;161(1):51-63. doi: 10.1007/BF00304668.
3
Nonlinear mechanical behaviour of the basilar membrane in the basal turn of the guinea pig cochlea.豚鼠耳蜗基底转中基底膜的非线性力学行为。
Hear Res. 1980 Jun;2(3-4):183-9. doi: 10.1016/0378-5955(80)90056-8.
4
Basilar-membrane motion in the alligator lizard: its relation to tonotopic organization and frequency selectivity.鳄蜥基底膜的运动:其与音频定位组织和频率选择性的关系。
J Acoust Soc Am. 1980 May;67(5):1736-45. doi: 10.1121/1.384300.
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Relations between frequency selectivity and two-tone rate suppression in lizard cochlear-nerve fibers.
Hear Res. 1980 Jan;2(1):21-38. doi: 10.1016/0378-5955(80)90014-3.
6
Cilium length: influence on neural tonotopic organization.纤毛长度:对神经音频定位组织的影响
Science. 1981 Sep 25;213(4515):1519-21. doi: 10.1126/science.7280673.
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The cochlear frequency map for the cat: labeling auditory-nerve fibers of known characteristic frequency.
J Acoust Soc Am. 1982 Nov;72(5):1441-9. doi: 10.1121/1.388677.
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Measurement of basilar membrane motion in the guinea pig using the Mössbauer technique.使用穆斯堡尔技术测量豚鼠基底膜运动。
J Acoust Soc Am. 1982 Jul;72(1):131-41. doi: 10.1121/1.387996.
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Basilar membrane tuning in the cat cochlea.猫耳蜗中的基底膜调谐。
Science. 1982 Jan 15;215(4530):305-6. doi: 10.1126/science.7053580.
10
Suggested evolution of tonotopic organization in the frog amphibian papilla.
Neurosci Lett. 1981 Jan 20;21(2):131-6. doi: 10.1016/0304-3940(81)90370-0.

鳄蜥耳蜗中毛细胞和神经纤维的频率选择性。

Frequency selectivity of hair cells and nerve fibres in the alligator lizard cochlea.

作者信息

Holton T, Weiss T F

出版信息

J Physiol. 1983 Dec;345:241-60. doi: 10.1113/jphysiol.1983.sp014976.

DOI:10.1113/jphysiol.1983.sp014976
PMID:6663500
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1193795/
Abstract

Receptor potentials of hair cells and spike discharges of cochlear nerve fibres were recorded with micropipettes from the free-standing region of the basilar papilla of anaesthetized alligator lizards in response to tones. In this region the hair-cell stereocilia are free-standing, i.e. they protrude directly into endolymph and are not in contact with a tectorial membrane. The frequency selectivity of hair-cell responses was measured by means of isovoltage contours of the d.c. (V0) and fundamental-a.c. (V1) component of the receptor potential, i.e. iso-V0 and iso-V1 contours. The frequency selectivity of the nerve-fibre discharge was measured by iso-rate (iso-V0) contours. Iso-V0, iso-V1 and iso-V0 contours are basically V-shaped with a characteristic frequency (c.f.) defined as the frequency at which minimum sound pressure (Pmin) is required to evoke the criterion value of the response. Receptor potential iso-V0 contours and neural iso-V0 contours have similar slopes: the mean slopes of the low-frequency sides (dB/decade) are -43.0 and -44.3; the slopes of the high-frequency sides are 85.0 and 80.2. The band widths of iso-V0 and iso-V0 contours away from c.f. are similar (mean values of Q30dB are 0.40 and 0.53, respectively). The band widths of iso-V0 contours near c.f. are narrower than those of iso-V0 contours (mean values of Q10dB are 2.34 and 1.20, respectively). However, the shapes of the contours near c.f. depend on the iso-response criteria, and we have not determined whether or not iso-V0 and iso-V0 contours are similar near c.f. The shapes of iso-V1 contours differ from those of iso-V0 and iso-V0 contours. Nerve fibre c.f.s are tonotopically organized in the nerve, with lowest c.f.s recorded from fibres innervating the border of free-standing and tectorial regions, a region in which hair-cell stereocilia are longest, and the highest c.f.s recorded from fibres innervating the end of the free-standing region in which hair-cell stereocilia are shortest. The c.f. of nerve-fibre response (and by implication hair-cell response) is, therefore, correlated with the height of the stereociliary tuft. The shapes of iso-V0 contours vary systematically with c.f. and, therefore, tonotopically with nerve position.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

用微电极从麻醉的美洲蜥蜴基底乳头的独立区域记录毛细胞的感受器电位和耳蜗神经纤维的锋电位发放,以响应纯音刺激。在该区域,毛细胞的静纤毛是独立的,即它们直接突入内淋巴,不与盖膜接触。毛细胞反应的频率选择性通过感受器电位的直流(V0)和基波交流(V1)成分的等电压轮廓来测量,即等V0和等V1轮廓。神经纤维放电的频率选择性通过等频率(等V0)轮廓来测量。等V0、等V1和等V0轮廓基本呈V形,特征频率(c.f.)定义为唤起反应标准值所需的最小声压(Pmin)的频率。感受器电位等V0轮廓和神经等V0轮廓具有相似的斜率:低频侧的平均斜率(dB/十年)分别为-43.0和-44.3;高频侧的斜率分别为85.0和80.2。远离c.f.的等V0和等V0轮廓的带宽相似(Q30dB的平均值分别为0.40和0.53)。靠近c.f.的等V0轮廓的带宽比等V0轮廓的窄(Q10dB的平均值分别为2.34和1.20)。然而,靠近c.f.的轮廓形状取决于等反应标准,我们尚未确定等V0和等V0轮廓在靠近c.f.处是否相似。等V1轮廓的形状与等V0和等V轮廓不同。神经纤维的c.f.s在神经中呈音频拓扑组织,从支配独立区域和盖膜区域边界的纤维记录到最低的c.f.s,该区域毛细胞的静纤毛最长,从支配独立区域末端的纤维记录到最高的c.f.s,该区域毛细胞的静纤毛最短。因此,神经纤维反应的c.f.(进而毛细胞反应的c.f.)与静纤毛束的高度相关。等V0轮廓的形状随c.f.系统变化,因此随神经位置呈音频拓扑变化。(摘要截断于400字)