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发育期早期,海藻酸对大鼠耳蜗的神经毒性作用。

Neurotoxicity of kainic acid in the rat cochlea during early developmental stages.

作者信息

Gil-Loyzaga P, Pujol R

机构信息

Laboratoire Neurobiologie de l'Audition, INSERM - U. 254 et Université de Montpellier II, Hôpital St. Charles, France.

出版信息

Eur Arch Otorhinolaryngol. 1990;248(1):40-8. doi: 10.1007/BF00634780.

Abstract

The neurotoxic effect of kainic acid (KA) was investigated by electron microscopy in rat cochleas at two developmental stages: 17 days of gestation (17 G) and postnatal day 1 (PN 1). In each animal, one cochlea was injected with 1 nmol KA diluted into 2 ml artificial perilymph, while the other cochlea was only injected with artificial perilymph as a control. Ten minutes later, the cochleas were perfused with fixative, removed and processed for electron microscopy. The KA injection resulted in marked swelling of the majority of afferent fibers, i.e. the peripheral processes of spiral ganglion neurons. In the 17 G cochlea, swollen fibers were traced from the perikarya to the undifferentiated otocyst epithelium. Following birth, swollen afferents in the PN 1 cochlea were in contact with both inner (IHCs) and outer hair cells (OHCs), which were now differentiated. At both stages of development, a subclass of small afferent nerves were unaffected. At PN 1, the KA-insensitive afferents only contacted the OHCs. These fibers probably belong to the spiral system of afferents and are related to type II spiral ganglion cells. Conversely, KA-sensitive afferents probably belong to the radial system, related to type I spiral ganglion cells. This system is specific for IHCs in adult cochleas and appears to innervate both IHCs and OHCs at early developmental stages. These findings also indicate that KA neurotoxicity appears very early in the cochlea, at a prenatal time (17 G) before the presynaptic partners of afferent terminals (namely the IHCs) are differentiated.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过电子显微镜研究了海藻酸(KA)在大鼠耳蜗两个发育阶段的神经毒性作用:妊娠17天(17G)和出生后第1天(PN1)。在每只动物中,一个耳蜗注射稀释于2ml人工外淋巴中的1nmol KA,而另一个耳蜗仅注射人工外淋巴作为对照。10分钟后,用固定剂灌注耳蜗,取出并进行电子显微镜处理。KA注射导致大多数传入纤维明显肿胀,即螺旋神经节神经元的外周突。在17G的耳蜗中,肿胀的纤维从胞体延伸至未分化的耳囊上皮。出生后,PN1耳蜗中肿胀的传入纤维与已分化的内毛细胞(IHCs)和外毛细胞(OHCs)均有接触。在两个发育阶段,一小类小传入神经未受影响。在PN1时,对KA不敏感的传入纤维仅与OHCs接触。这些纤维可能属于传入螺旋系统,与II型螺旋神经节细胞有关。相反,对KA敏感的传入纤维可能属于放射状系统,与I型螺旋神经节细胞有关。该系统在成年耳蜗中对IHCs具有特异性,在发育早期似乎同时支配IHCs和OHCs。这些发现还表明,KA神经毒性在耳蜗中很早就出现了,即在传入终末的突触前伙伴(即IHCs)分化之前的产前时期(17G)。(摘要截断于250字)

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