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1.
Brain Behav ; 9(8): e01353, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31271523

RESUMEN

INTRODUCTION: Cochlear ablation causing sensory deafferentation (SD) of the cochlear nucleus triggers complex re-arrangements in the cellular and molecular communication networks of the adult mammalian central auditory system. Participation of the extracellular matrix (ECM) in these processes is not well understood. METHODS: We investigated consequences of unilateral SD for the expression and distribution of the chondroitin sulfate proteoglycans, neurocan (Ncan) and aggrecan (Agg), alongside various plasticity markers in the auditory brainstem of the adult rat using immunohistochemical techniques. RESULTS: In the deafferented ventral cochlear nucleus (VCN), Ncan expression increased massively within 3 postoperative days (POD), but rapidly decreased thereafter. Agg showed a similar but less pronounced progression. Decrease in Ncan was spatially and temporally related to the re-innervation of VCN documented by the emergence of growth-associated protein Gap43 contained in nerve fibers and presynaptic boutons. Concurrently, astrocytes grew and expressed matrix metalloproteinase-2 (MMP2), an enzyme known to emerge only under re-innervation of VCN. MMP2 is capable of cleaving both Ncan and Agg when released. A transient modulation of the ECM in the central inferior colliculus on the side opposite to SD occurred by POD1. Modulations of glutamatergic synapses and Gap43 expression were detected, reflecting state changes of the surrounding tissue induced by transsynaptic effects of SD. CONCLUSIONS: The ECM variously participates in adaptive responses to sudden deafness by SD on several levels along the central auditory pathway, with a striking spatial and temporal relationship of Ncan modulation to astrocytic activation and to synaptogenesis.


Asunto(s)
Astrocitos/metabolismo , Vías Auditivas/metabolismo , Tronco Encefálico/metabolismo , Núcleo Coclear/metabolismo , Neurocano/metabolismo , Vías Aferentes/metabolismo , Agrecanos/metabolismo , Animales , Femenino , Metaloproteinasa 2 de la Matriz/metabolismo , Neurogénesis/fisiología , Ratas , Ratas Wistar
2.
Eur J Neurosci ; 50(12): 3985-4003, 2019 12.
Artículo en Inglés | MEDLINE | ID: mdl-31325398

RESUMEN

A complex scenario of cellular network reorganization is caused by unilateral sensory deafferentation (USD) in the adult rat central auditory system. We asked whether this plasticity response involves mitosis. Immunohistochemistry was applied to brainstem sections for the detection and localization of mitotic markers Ki67 and PCNA, the growth-associated protein Gap43 and purine receptor P2X4. Fluorescent double staining was done for Ki67:PCNA and for both of them with HuC/HuD (neurons), S100 (astrocytes), Iba1 (microglia) and P2X4. Inquiring 1-7 days after USD, we found Ki67 expression to be changed in cellular profiles of cochlear nucleus (CN) with a significant increase in number by 1-3 days, followed by reset to control level within 1 week. USD-induced mitosis exclusively occurred in microglia and was absent elsewhere in the auditory brainstem. PCNA staining of small cellular profiles increased similarly but remained elevated. PCNA staining intensity also changed in CN, superior olive and inferior colliculus in neuronal nuclei, suggesting shifts in DNA processing. No apoptotic cell death was detected in any region of the adult auditory brainstem after USD. A comparison of anterograde and retrograde effects of nerve damage revealed proliferating microglia expressing P2X4 receptors in CN upon USD, but not in the facial nucleus after facial nerve transection. In conclusion, the deafferentation model studied here permits insight into the capacity of the adult mammalian brain to invoke mitosis among glia cells, adjustment of gene processing in neurons and purinergic signalling between them, jointly accounting for a multilayered neuro- and glioplastic response.


Asunto(s)
Astrocitos/metabolismo , Tronco Encefálico/metabolismo , ADN/metabolismo , Neuronas/metabolismo , Animales , Vías Auditivas/metabolismo , Núcleo Coclear/metabolismo , Colículos Inferiores/metabolismo , Microglía/metabolismo , Ratas
3.
Neuroscience ; 400: 1-16, 2019 02 21.
Artículo en Inglés | MEDLINE | ID: mdl-30594562

RESUMEN

Worldwide, almost 500 million people are hearing impaired, making hearing loss the most common sensory impairment among humans. For people with single-sided deafness (SSD), cochlear implants (CIs) can be enormously beneficial by providing binaural information. However, binaural benefits in CI users have been only incompletely realized. Overcoming these limitations requires a better knowledge of how neuronal circuits adapt to SSD and how unilateral CI stimulation can compensate a deaf ear. We investigated effects of neonatal SSD on auditory brainstem circuitry using acoustic (AS), electric (ES), or acoustic stimulation on one ear and electric stimulation on the other ear (AS + ES). The molecular marker Fos was used to investigate changes in interneuronal communication due to SSD. To induce SSD, neonatal rats obtained a unilateral intracochlear injection of neomycin. In adulthood, rats were acutely stimulated by AS, ES, or AS + ES. AS and ES were applied correspondingly in terms of intracochlear stimulation side and intensity resulting in bilaterally comparable Fos expression in hearing rats. In contrast, SSD rats showed a loss of tonotopic order along the deafened pathway, indicated by a massive increase and spread of Fos expressing neurons. We report three major results: First, AS of the hearing ear of SSD rats resulted in bilateral activation of neurons in the cochlear nucleus (CN). Second, ES of the deaf ear did not activate contralateral CN. Third, AS + ES of SSD rats resulted in bilateral reduced Fos expression in the auditory brainstem compared to monaural stimulations. These findings indicate changes in inhibitory interactions among neuronal networks as a result of monaural deafness.


Asunto(s)
Núcleo Coclear/fisiopatología , Sordera/fisiopatología , Neuronas/fisiología , Estimulación Acústica , Animales , Vías Auditivas/fisiopatología , Implantación Coclear , Estimulación Eléctrica , Potenciales Evocados Auditivos del Tronco Encefálico , Femenino , Lateralidad Funcional , Masculino , Proteínas Proto-Oncogénicas c-fos/metabolismo , Ratas Wistar
4.
Front Cell Neurosci ; 12: 43, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29520220

RESUMEN

Neuron-glia interactions contribute to tissue homeostasis and functional plasticity in the mammalian brain, but it remains unclear how this is achieved. The potential of central auditory brain tissue for stimulation-dependent cellular remodeling was studied in hearing-experienced and neonatally deafened rats. At adulthood, both groups received an intracochlear electrode into the left cochlea and were continuously stimulated for 1 or 7 days after waking up from anesthesia. Normal hearing and deafness were assessed by auditory brainstem responses (ABRs). The effectiveness of stimulation was verified by electrically evoked ABRs as well as immunocytochemistry and in situ hybridization for the immediate early gene product Fos on sections through the auditory midbrain containing the inferior colliculus (IC). Whereas hearing-experienced animals showed a tonotopically restricted Fos response in the IC contralateral to electrical intracochlear stimulation, Fos-positive neurons were found almost throughout the contralateral IC in deaf animals. In deaf rats, the Fos response was accompanied by a massive increase of GFAP indicating astrocytic hypertrophy, and a local activation of microglial cells identified by IBA1. These glia responses led to a noticeable increase of neuron-glia approximations. Moreover, staining for the GABA synthetizing enzymes GAD65 and GAD67 rose significantly in neuronal cell bodies and presynaptic boutons in the contralateral IC of deaf rats. Activation of neurons and glial cells and tissue re-composition were in no case accompanied by cell death as would have been apparent by a Tunel reaction. These findings suggest that growth and activity of glial cells is crucial for the local adjustment of neuronal inhibition to neuronal excitation.

5.
Hear Res ; 333: 210-215, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26386286

RESUMEN

Aim of this study was to induce a single-sided deafness (SSD) in rats before hearing onset. Rats were operated at postnatal day 10 by approaching the tympanic cavity along a retroauricular path without manipulating ossicles or tympanic membrane. The ototoxic aminoglycoside neomycin was injected intracochlearly through the round window membrane on one side. When the animals have reached young adult stages, their hearing threshold was determined by their auditory brainstem response (ABR). Monaural deafening was considered successful when the hearing threshold was at least 95 dB above the threshold of the normal hearing ear. Growing up with one non-functional ear, rats developed a striking anatomical asymmetry of their cochlear nuclei (CN). The CN from age-matched normal hearing brains and from both sides of single-sided deaf brains were cut into series of frontal sections and their volumes calculated. No difference was detected between the volume of the normal hearing CN and the contralateral CN in SSD rats. By contrast, growth retardation was found for the ventral CN on the deaf side to result in a volume of only 57% compared to the normal hearing side. Marginal growth retardation was also observed for the dorsal CN on the deaf side. Thus, loss of sensory activation leads mainly, but not exclusively, to a reduction of tissue volume in the ventral CN of the deaf side, leaving the contralateral side apparently unaffected.


Asunto(s)
Núcleo Coclear/patología , Pérdida Auditiva Unilateral/patología , Estimulación Acústica , Factores de Edad , Animales , Animales Recién Nacidos , Umbral Auditivo , Núcleo Coclear/crecimiento & desarrollo , Modelos Animales de Enfermedad , Potenciales Evocados Auditivos del Tronco Encefálico , Femenino , Audición , Pérdida Auditiva Unilateral/inducido químicamente , Pérdida Auditiva Unilateral/fisiopatología , Pérdida Auditiva Unilateral/psicología , Masculino , Neomicina , Tamaño de los Órganos , Ratas Wistar
6.
Exp Neurol ; 266: 55-67, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-25708983

RESUMEN

The immediate-early-gene c-fos with its protein product Fos has been used as a powerful tool to investigate neuronal activity and plasticity following sensory stimulation. Fos combines with Jun, another IEG product, to form the dimeric transcription factor activator protein 1 (AP-1) which has been implied in a variety of cellular functions like neuronal plasticity, apoptosis, and regeneration. The intracellular emergence of Fos indicates a functional state of nerve cells directed towards molecular and morphological changes. The central auditory system is construed to detect stimulus intensity, spectral composition, and binaural balance through neurons organized in a complex network of ascending, descending and commissural pathways. Here we compare monaural and binaural electrical intracochlear stimulation (EIS) in normal hearing and early postnatally deafened rats. Binaural stimulation was done either synchronously or asynchronously. The auditory brainstem of hearing and deaf rats responds differently, with a dramatically increasing Fos expression in the deaf group so as if the network had no pre-orientation for how to organize sensory activity. Binaural EIS does not result in a trivial sum of 2 independent monaural EIS, as asynchronous stimulation invokes stronger Fos activation compared to synchronous stimulation almost everywhere in the auditory brainstem. The differential response to synchronicity of the stimulation puts emphasis on the importance of the temporal structure of EIS with respect to its potential for changing brain structure and brain function in stimulus-specific ways.


Asunto(s)
Vías Auditivas/metabolismo , Cóclea/efectos de los fármacos , Potenciales Evocados Auditivos del Tronco Encefálico/efectos de los fármacos , Regulación de la Expresión Génica/efectos de los fármacos , Genes fos/efectos de los fármacos , Animales , Corteza Auditiva/efectos de los fármacos , Corteza Auditiva/metabolismo , Vías Auditivas/efectos de los fármacos , Tronco Encefálico/metabolismo , Núcleo Coclear/efectos de los fármacos , Núcleo Coclear/metabolismo , Sordera/fisiopatología , Estimulación Eléctrica , Colículos Inferiores/efectos de los fármacos , Colículos Inferiores/metabolismo , Martillo/fisiopatología , Núcleo Olivar/efectos de los fármacos , Núcleo Olivar/metabolismo , Ratas , Ratas Wistar
7.
PLoS One ; 9(3): e92624, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24647228

RESUMEN

Brain development and learning is accompanied by morphological and molecular changes in neurons. The growth associated protein 43 (Gap43), indicator of neurite elongation and synapse formation, is highly expressed during early stages of development. Upon maturation of the brain, Gap43 is down-regulated by most neurons with the exception of subdivisions such as the CA3 region of hippocampus, the lateral superior olive (LSO) and the central inferior colliculus (CIC). Little is known about the regulation of this mRNA in adult brains. We found that the expression of Gap43 mRNA in specific neurons can be modulated by changing sensory activity of the adult brain. Using the central auditory system of rats as a model, Gap43 protein and mRNA levels were determined in LSO and CIC of hearing-experienced rats unilaterally or bilaterally deafened or unilaterally stimulated by a cochlear implant (CI). Our data indicate that Gap43 is a marker useful beyond monitoring neuronal growth and synaptogenesis, reflecting also specific patterns of synaptic activities on specific neurons. Thus, unilateral loss of input to an adult auditory system directly causes asymmetrical expression of Gap43 mRNA between LSOs or CICs on both sides of the brainstem. This consequence can be prevented by simple-patterned stimulation of a dysfunctional ear by way of a CI. We suggest that as a function of input balance and activity pattern, Gap43 mRNA expression changes as cells associate converging afferent signals.


Asunto(s)
Encéfalo/metabolismo , Proteína GAP-43/metabolismo , Animales , Vías Auditivas , Tronco Encefálico/metabolismo , Femenino , Colículos Inferiores/metabolismo , Ratas , Ratas Wistar
8.
J Neurosci Res ; 92(4): 432-45, 2014 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-24446187

RESUMEN

Cochlear ablation triggers cellular and molecular reactions in the adult mammalian central auditory system, leading to complex rearrangements in the cellular networks of the auditory brainstem. The role of microglial cells in these processes is largely unknown. We analyzed morphological and molecular responses as well as cellular affiliations of microglia in the auditory brainstem 1 and 7 days after unilateral sensory deafferentation of the cochlear nucleus. In the ventral cochlear nucleus (VCN), morphological changes of microglial cells were evident following cochlear ablation. Microglial activation preceded astroglial hypertrophy in VCN and lateral superior olive (LSO). During axonal degeneration in VCN early after cochlear ablation, p-ERK1/2- and p-p38-immunoreactive microglia displayed a hypertrophied phenotype, with processes partially surrounding glutamatergic but not GABAergic synapses. During the peak of VCN reinnervation 1 week after cochlear ablation, the number of microglial cells increased massively. Microglia now displayed dense ramifications juxtaposed to Gap43-immunoreactive axons and their terminals. Moreover, we identified lesion-dependent changes in the populations of microglia and astrocytes in LSO and inferior colliculus. By covisualizing cytological markers such as NeuN, GFAP, CD11b, vGluT-1, GAD-65, and Gap43 with the prominent MAP kinases ERK1/2 and p38, we show that MAPK signaling is affected by sensory deafferentation in microglia but not in astroglia or in neurons. In conclusion, microglia displaying MAPK signaling appear to contribute to an adaptive response in central auditory regions that was directly or indirectly affected by sensory deafferentation. Moreover, microglial cells are temporally and spatially in place to participate in synaptogenesis inside VCN.


Asunto(s)
Núcleo Coclear/citología , Microglía/fisiología , Red Nerviosa/fisiología , Neuronas/fisiología , Factores de Edad , Análisis de Varianza , Animales , Animales Recién Nacidos , Cóclea/inervación , Cóclea/cirugía , Nervio Coclear/citología , Nervio Coclear/fisiología , Desnervación , Femenino , Proteínas del Tejido Nervioso/metabolismo , Ratas , Ratas Wistar
9.
Eur J Neurosci ; 38(1): 2041-56, 2013 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-23581580

RESUMEN

Ablating the cochlea causes total sensory deafferentation of the cochlear nucleus. Over the first postoperative week, degeneration of the auditory nerve and its synaptic terminals in the cochlear nucleus temporally overlaps with its re-innervation by axon collaterals of medial olivocochlear neurons. At the same time, astrocytes increase in size and density. We investigated the time courses of the expression of ezrin, polysialic acid, matrix metalloprotease-9 and matrix metalloprotease-2 within these astrocytes during the first week following cochlear ablation. All four proteins are known to participate in degeneration, regeneration, or both, following injury of the central nervous system. In a next step, stereotaxic injections of kainic acid were made into the ventral nucleus of the trapezoid body prior to cochlear ablation to destroy the neurons that re-innervate the deafferented cochlear nucleus by axon collaterals developing growth-associated protein 43 immunoreactivity. This experimental design allowed us to distinguish between molecular processes associated with degeneration and those associated with re-innervation. Under these conditions, astrocytic growth and proliferation showed an unchanged deafferentation-induced pattern. Similarly, the distribution and amount of ezrin and matrix metalloprotease-9 in astrocytes after cochlear ablation developed in the same way as under cochlear ablation alone. In sharp contrast, the astrocytic expression of polysialic acid and matrix metalloprotease-2 normally invoked by cochlear ablation collapsed when re-innervation of the cochlear nucleus was inhibited by lesioning medial olivocochlear neurons with kainic acid. In conclusion, re-innervation, including axonal growth and synaptogenesis, seems to prompt astrocytes to recompose their molecular profile, paving the way for tissue reorganisation after nerve degeneration and loss of synaptic contacts.


Asunto(s)
Astrocitos/metabolismo , Núcleo Coclear/fisiología , Neuronas Aferentes/fisiología , Animales , Astrocitos/fisiología , Axones/efectos de los fármacos , Axones/fisiología , Proliferación Celular , Cóclea/inervación , Nervio Coclear/citología , Nervio Coclear/fisiología , Núcleo Coclear/citología , Núcleo Coclear/metabolismo , Proteínas del Citoesqueleto/genética , Proteínas del Citoesqueleto/metabolismo , Desnervación , Femenino , Proteína GAP-43/genética , Proteína GAP-43/metabolismo , Ácido Kaínico/toxicidad , Metaloproteinasa 2 de la Matriz/genética , Metaloproteinasa 2 de la Matriz/metabolismo , Metaloproteinasa 9 de la Matriz/genética , Metaloproteinasa 9 de la Matriz/metabolismo , Regeneración Nerviosa , Neuronas Aferentes/efectos de los fármacos , Ratas , Ratas Wistar , Ácidos Siálicos/metabolismo
10.
Brain Res ; 1435: 40-55, 2012 Jan 30.
Artículo en Inglés | MEDLINE | ID: mdl-22177665

RESUMEN

In this study we investigated the pattern of c-Fos expression in anteroventral (AVCN) and dorsal cochlear nucleus (DCN) and central inferior colliculus (CIC) following electrical intracochlear stimulation (EIS) of anesthetized adult rats that were neonatally deafened. The animals never experienced acoustic sensations as their hair cells were destroyed by daily kanamycin injections between postnatal days 10 to 20, resulting in a rise of hearing threshold by about 90 dB. Unilateral EIS was applied through a cochlear implant inserted into the medial turn of the left cochlea and lasted for 45 or 73 min, 2, 3:15, or 5h. Following EIS at 50Hz, a high number of c-Fos positive nuclei were observed showing only marginal tonotopic order in ipsilateral AVCN, in DCN bilaterally, and in contralateral CIC. Quantifying the number of c-Fos positive nuclei in ipsilateral AVCN, we found a steady increase with stimulation time. By contrast, the population of neurons expressing c-Fos in DCN and CIC revealed a transient maximum at 73 min. A direct comparison with our previous study (Rosskothen-Kuhl, N., Illing, R.-B., 2010. Nonlinear development of the populations of neurons expressing c-Fos under sustained electrical intracochlear stimulation in the rat auditory brainstem. Brain Res. 1347, 33-41) reveals that absence of hearing experience has far-reaching consequences for the interneuronal communication within networks of the auditory brainstem. When hearing fails, EIS entails expression of c-Fos in populations of neurons that are much larger than normally, essentially disregard tonotopic order, and lack much of spatio-temporal variations seen in hearing-experienced rats.


Asunto(s)
Núcleo Coclear/patología , Sordera/patología , Sordera/fisiopatología , Colículos Inferiores/patología , Neuronas/metabolismo , Proteínas Proto-Oncogénicas c-fos/metabolismo , Estimulación Acústica/métodos , Análisis de Varianza , Animales , Animales Recién Nacidos , Umbral Auditivo/fisiología , Cóclea/fisiología , Implantes Cocleares , Sordera/inducido químicamente , Sordera/cirugía , Modelos Animales de Enfermedad , Estimulación Eléctrica , Femenino , Lateralidad Funcional/fisiología , Regulación de la Expresión Génica/fisiología , Kanamicina/toxicidad , Masculino , Ratas , Ratas Wistar , Factores de Tiempo
11.
Neural Plast ; 2011: 859359, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-22135757

RESUMEN

The matrix metalloproteinases MMP-9 and MMP-2, major modulators of the extracellular matrix (ECM), were changed in amount and distribution in the rat anteroventral cochlear nucleus (AVCN) following its sensory deafferentation by cochlear ablation. To determine what causal relationships exist between the redistribution of MMP-9 and MMP-2 and deafferentation-induced reinnervation, kainic acid was stereotaxically injected into the ventral nucleus of the trapezoid body (VNTB) prior to cochlear ablation, killing cells that deliver the growth associated protein 43 (GAP-43) into AVCN. Deafferentation-induced changes in the pattern of MMP-9 staining remained unaffected by VNTB lesions. By contrast, changes in the distribution of MMP-2 normally evoked by sensory deafferentation were reversed if GAP-43 positive axons were prevented to grow in AVCN. In conclusion, GAP-43-containing axons emerging in AVCN after cochlear ablation seem to be causal for the maintenance of MMP-2-mediated ECM remodeling.


Asunto(s)
Axones/metabolismo , Núcleo Coclear/enzimología , Proteína GAP-43/metabolismo , Metaloproteinasa 2 de la Matriz/metabolismo , Metaloproteinasa 9 de la Matriz/metabolismo , Animales , Núcleo Coclear/metabolismo , Ácido Kaínico/administración & dosificación , Cinética , Ratas
12.
PLoS One ; 6(8): e23686, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21887295

RESUMEN

Ablation of a cochlea causes total sensory deafferentation of the cochlear nucleus in the brainstem, providing a model to investigate nervous degeneration and formation of new synaptic contacts in the adult brain. In a quantitative electron microscopical study on the plasticity of the central auditory system of the Wistar rat, we first determined what fraction of the total number of synaptic contact zones (SCZs) in the anteroventral cochlear nucleus (AVCN) is attributable to primary sensory innervation and how many synapses remain after total unilateral cochlear ablation. Second, we attempted to identify the potential for a deafferentation-dependent synaptogenesis. SCZs were ultrastructurally identified before and after deafferentation in tissue treated for ethanolic phosphotungstic acid (EPTA) staining. This was combined with pre-embedding immunocytochemistry for gephyrin identifying inhibitory SCZs, the growth-associated protein GAP-43, glutamate, and choline acetyltransferase. A stereological analysis of EPTA stained sections revealed 1.11±0.09 (S.E.M.)×10(9) SCZs per mm(3) of AVCN tissue. Within 7 days of deafferentation, this number was down by 46%. Excitatory and inhibitory synapses were differentially affected on the side of deafferentation. Excitatory synapses were quickly reduced and then began to increase in number again, necessarily being complemented from sources other than cochlear neurons, while inhibitory synapses were reduced more slowly and continuously. The result was a transient rise of the relative fraction of inhibitory synapses with a decline below original levels thereafter. Synaptogenesis was inferred by the emergence of morphologically immature SCZs that were consistently associated with GAP-43 immunoreactivity. SCZs of this type were estimated to make up a fraction of close to 30% of the total synaptic population present by ten weeks after sensory deafferentation. In conclusion, there appears to be a substantial potential for network reorganization and synaptogenesis in the auditory brainstem after loss of hearing, even in the adult brain.


Asunto(s)
Vías Auditivas/fisiopatología , Núcleo Coclear/fisiología , Sinapsis/metabolismo , Vías Aferentes/fisiopatología , Animales , Tronco Encefálico/fisiopatología , Proteína GAP-43/metabolismo , Pérdida Auditiva/fisiopatología , Microscopía Electrónica , Ratas , Ratas Wistar
13.
Brain Res ; 1347: 33-41, 2010 Aug 06.
Artículo en Inglés | MEDLINE | ID: mdl-20570662

RESUMEN

The immediate-early-gene c-fos is among the first genes to be expressed following sensory-invoked neuronal activity. Its gene product c-Fos forms the limiting monomer of the heterodimeric activator protein-1 transcription factor that triggers various genes involved in neuroplastic remodeling. This study investigated the pattern of c-Fos expression in anteroventral (AVCN) and dorsal cochlear nucleus (DCN) and central inferior colliculus (CIC) after 45 min, 73 min, 2 h, 3:15 h and 5 h of unilateral electrical intracochlear stimulation (EIS) at 50 Hz in anaesthetized rats. Following EIS, tonotopic c-Fos expression was observed for each stimulation time in ipsilateral AVCN, DCN bilaterally, and contralateral CIC. By counting c-Fos positive nuclei, we discovered temporal non-linearities in the size of the respective population of c-Fos expressing neurons. In all regions investigated, the populations significantly increased from 73 min to 2 h but decreased towards 3:15 h. In AVCN, the number rose again by 5 h of EIS. Remarkably, the same was noted for neurons with large nuclei in deep DCN. In both regions, the population of responsive neurons shifted spatially: In central AVCN, the density of c-Fos positive cells increased significantly from 2 to 5h with medial and lateral regions remaining unchanged. In DCN, the density of large c-Fos positive nuclei fell in the upper and rose in the deep layers from 45 min to 5h of EIS. In conclusion, spatiotemporally varying recruitments of neuronal subpopulations into cellular networks responding to specific patterns of sensory activity take place in the auditory brainstem.


Asunto(s)
Núcleo Coclear/fisiología , Regulación de la Expresión Génica/fisiología , Colículos Inferiores/citología , Colículos Inferiores/fisiología , Plasticidad Neuronal/fisiología , Neuronas/fisiología , Proteínas Proto-Oncogénicas c-fos/metabolismo , Análisis de Varianza , Animales , Vías Auditivas/fisiología , Recuento de Células/métodos , Estimulación Eléctrica/métodos , Femenino , Lateralidad Funcional , Dinámicas no Lineales , Ratas , Ratas Wistar , Factores de Tiempo , Factor de Transcripción AP-1/metabolismo
14.
Neuroreport ; 21(5): 324-7, 2010 Mar 31.
Artículo en Inglés | MEDLINE | ID: mdl-20173666

RESUMEN

Lesion-induced neuroplasticity, including fiber degeneration, axonal growth, and synaptogenesis, involves dynamical changes of the extracellular matrix. We discovered that the matrix metalloprotease-2 (MMP-2), a major actor in extracellular matrix recomposition, is changed in distribution and increased in amount in the ventral cochlear nucleus after unilateral cochlear ablation. There was a remarkable coincidence of MMP-2 accumulation and GAP-43 expression in time and space. We obtained evidence indicating that MMP-2 is delivered to regions of emerging GAP-43 positive synaptic endings by postsynaptic neurons as well as by adjoining astrocytes. These results indicate a major role of MMP-2 in lesion-induced remodeling of central auditory networks and suggest a cooperativity with GAP-43-directed axonal outgrowth and synaptogenesis.


Asunto(s)
Cóclea/fisiopatología , Proteína GAP-43/metabolismo , Metaloproteinasa 2 de la Matriz/metabolismo , Plasticidad Neuronal/fisiología , Neuronas/fisiología , Sinapsis/fisiología , Animales , Astrocitos/fisiología , Axones/fisiología , Cóclea/lesiones , Técnica del Anticuerpo Fluorescente , Ratas , Ratas Wistar , Factores de Tiempo
15.
Exp Brain Res ; 195(2): 241-60, 2009 May.
Artículo en Inglés | MEDLINE | ID: mdl-19340418

RESUMEN

The nuclei of the auditory brainstem harbor a diversity of neuronal cell types and are interconnected by excitatory as well as inhibitory ascending, descending, and commissural pathways. Classically, neurons have been characterized by size and shape of their cell body and by the geometry of their dendrites. Our study is based on the use of axonal tracers in combination with immunocytochemistry to identify and distinguish neuronal subtypes by their molecular signature in dorsal and ventral cochlear nucleus, lateral superior olive, medial superior olive, medial nucleus of the trapezoid body, and inferior colliculus of the adult rat. The presumed neurotransmitters glutamate, glycine, and GABA were used alongside the calcium-binding proteins parvalbumin, calretinin, and calbindin-D28k as molecular markers. Our data provide distinct extensions to previous characterizations of neuronal subtypes and reveal regularities and differences across auditory brainstem nuclei that are discussed for their functional implications.


Asunto(s)
Vías Auditivas/citología , Axones/fisiología , Tronco Encefálico/citología , Neuronas/citología , Neuronas/fisiología , Animales , Vías Auditivas/anatomía & histología , Vías Auditivas/fisiología , Tronco Encefálico/anatomía & histología , Tronco Encefálico/fisiología , Calbindina 1 , Calbindina 2 , Calbindinas , Fluorescencia , Ácido Glutámico/metabolismo , Glicina/metabolismo , Inmunohistoquímica , Microscopía Fluorescente , Parvalbúminas/metabolismo , Ratas , Ratas Wistar , Proteína G de Unión al Calcio S100/metabolismo , Ácido gamma-Aminobutírico/metabolismo
16.
Neuroreport ; 19(11): 1091-3, 2008 Jul 16.
Artículo en Inglés | MEDLINE | ID: mdl-18596606

RESUMEN

Acoustical or intracochlear stimulation may induce expression of the immediate early gene product c-Fos in neurons throughout the auditory brainstem. Attempting to estimate its consequences, we sought to determine if c-Fos expression occurs in neurons that also contain c-Jun p39 with which it could form the heterodimeric transcription factor AP-1 to activate a large number of genes, among them several involved in neuroplastic remodeling. Following intracochlear stimulation, c-Fos and c-Jun were found to be colocalized in nuclei of many neurons at all levels of the subcortical auditory system. We conclude that stimulation triggers Fos-Jun dimerization, causing cascades of gene expression that potentially culminate in structural changes of neurons affected by the specific pattern of activity imposed on the neuronal system.


Asunto(s)
Vías Auditivas/metabolismo , Neuronas/metabolismo , Proteínas Proto-Oncogénicas c-fos/metabolismo , Proteínas Proto-Oncogénicas c-jun/metabolismo , Factor de Transcripción AP-1/metabolismo , Animales , Vías Auditivas/anatomía & histología , Vías Auditivas/citología , Tronco Encefálico/anatomía & histología , Tronco Encefálico/citología , Tronco Encefálico/metabolismo , Núcleo Coclear/citología , Núcleo Coclear/metabolismo , Núcleo Coclear/fisiología , Dimerización , Estimulación Eléctrica , Electrodos Implantados , Proteínas Inmediatas-Precoces/metabolismo , Proteínas Inmediatas-Precoces/fisiología , Inmunohistoquímica , Neuronas/citología , Neuronas/fisiología , Proteínas Proto-Oncogénicas c-fos/química , Proteínas Proto-Oncogénicas c-fos/fisiología , Proteínas Proto-Oncogénicas c-jun/química , Proteínas Proto-Oncogénicas c-jun/fisiología , Ratas , Ratas Wistar , Factor de Transcripción AP-1/fisiología
17.
Exp Neurol ; 208(2): 193-206, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17825819

RESUMEN

Specific patterns of sensory activity may induce plastic remodeling of neurons and the communication network they form in the adult mammalian brain. Among the indicators for the initiation of neuronal remodeling is the expression of immediate early genes (IEGs). The IEGs c-fos and egr-1 encode transcription factors. Following spectrally and temporally precisely defined unilateral electrical intracochlear stimulation (EIS) that corresponded in strength to physiological acoustic stimuli and lasted for 2 h under anesthesia, we characterized those neuronal cell types in ventral (VCN) and dorsal cochlear nucleus (DCN), lateral superior olive (LSO) and central nucleus of the inferior colliculus (CIC) of the rat brain that expressed IEGs. We found that EIS affected only specific types of neurons. Whereas sub-populations of glutamatergic and glycinergic cells responded in all four regions, GABAergic neurons failed to do so except in DCN. Combining immunocytochemistry with axonal tracing, neurons participating in major ascending pathways, commissural cells of VCN and certain types of neurons of the descending auditory system were seen to respond to EIS with IEG expression. By contrast, principal LSO cells projecting to the contralateral CIC as well as collicular efferents of the DCN did not. In total, less than 50% of the identified neurons turned up expression of the IEGs studied. The pattern of IEG expression caused by unilateral EIS led us to suggest that dominant sensory activity may quickly initiate a facilitation of central pathways serving the active ear at the expense of those serving the unstimulated ear.


Asunto(s)
Vías Auditivas/metabolismo , Tronco Encefálico/metabolismo , Cóclea/fisiología , Expresión Génica , Genes Inmediatos-Precoces , Neuronas/metabolismo , Animales , Vías Auditivas/citología , Tronco Encefálico/citología , Núcleo Coclear/metabolismo , Proteína 1 de la Respuesta de Crecimiento Precoz/metabolismo , Estimulación Eléctrica , Femenino , Inmunohistoquímica , Colículos Inferiores/metabolismo , Plasticidad Neuronal/fisiología , Núcleo Olivar/metabolismo , Proteínas Proto-Oncogénicas c-fos/metabolismo , Ratas , Ratas Wistar , Distribución Tisular
18.
Eur J Neurosci ; 23(12): 3187-99, 2006 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-16820009

RESUMEN

Recent studies suggest a potential for activity-dependent reconstruction in the adult mammalian brainstem that exceeds previous expectations. We found that a unilateral cochlear lesion led within 1 week to a rise of choline acetyltransferase (ChAT) immunoreactivity in the ventral cochlear nucleus of the affected side, matching the lesion-induced expression of growth-associated protein 43 (GAP-43) previously described. The rise of both ChAT and GAP-43 immunoreactivity was reflected in the average density of the staining. Moreover, the number of light-microscopically identifiable boutons increased in both stains. GAP-43-positive boutons could, by distinct ultrastructural features, regularly be identified as presynaptic endings. However, GAP-43 immunoreactivity was not only found in presynaptic endings with a classical morphology, but also in profiles that suggest morphological dynamic structures by showing filopodia, assemblages of pleomorphic vesicles, large vesicles (diameter up to 200 nm) fusing with the presynaptic plasma membrane close to synaptic contacts, small dense-core vesicles (diameter about 80 nm) and presynaptic ribosomes. Moreover, we observed perforated synapses as well as GAP-43 immunoreactivity condensed in rafts, both indicative of growing or changing neuronal connections. Classical and untypical ultrastructural profiles that contained GAP-43 also contained ChAT. We conclude that there is extensive deafness-induced GAP-43-mediated synaptic plasticity in the cochlear nucleus, and that this plasticity is predominantly, if not exclusively, based on cholinergic afferents.


Asunto(s)
Colina O-Acetiltransferasa/metabolismo , Cóclea/patología , Núcleo Coclear/metabolismo , Proteína GAP-43/metabolismo , Sinapsis/metabolismo , Acetilcolina/metabolismo , Animales , Cóclea/citología , Cóclea/metabolismo , Núcleo Coclear/ultraestructura , Inmunohistoquímica , Plasticidad Neuronal/fisiología , Neuronas/metabolismo , Neuronas/ultraestructura , Ratas , Ratas Wistar , Sinapsis/química , Sinapsis/ultraestructura
19.
Hear Res ; 216-217: 189-97, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-16624512

RESUMEN

Variations of sensory activation in strength and pattern are known to affect structure and function of the mammalian brain. Whereas such malleability is readily granted to forebrain structures at early developmental stages, acceptance of experience-dependent structural plasticity has been slow for the adult brainstem. Over the past years we have identified consequences of cochlear ablation, noise trauma, or electrical intracochlear stimulation on neurons and circuitry of the auditory brainstem of the adult rat. We found that loss of sensory activation as well as a substitution for it entail specific molecular, ultrastructural, and morphological changes to central auditory neurons. Here, we make a first attempt to compare these different patterns of central remodeling. We tentatively suggest that after hearing loss or intracochlear stimulation responses of the central neural network in the adult brainstem suit the concept of functional adaptation.


Asunto(s)
Núcleo Coclear/metabolismo , Pérdida Auditiva/fisiopatología , Plasticidad Neuronal/fisiología , Animales , Cóclea/fisiología , Cóclea/cirugía , Implantes Cocleares , Núcleo Coclear/ultraestructura , Estimulación Eléctrica , Proteína GAP-43/metabolismo , Pérdida Auditiva/rehabilitación , Inmunohistoquímica , Microscopía Electrónica , Ratas , Ratas Wistar , Sinapsis/fisiología , Transmisión Sináptica/fisiología
20.
Hear Res ; 206(1-2): 185-99, 2005 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-16081008

RESUMEN

When we disturbed the auditory input of the adult rat by cochleotomy or noise trauma on one side, several substantial anatomical, cellular, and molecular changes took place in the auditory brainstem. We found that: (1) cochleotomy or severe noise trauma both lead to a considerable increase of immunoreactivity of the growth-associated protein GAP-43 in the ventral cochlear nucleus (VCN) of the affected side; (2) the expression of GAP-43 in VCN is restricted to presynaptic endings and short fiber segments; (3) axon collaterals of the cholinergic medial olivocochlear (MOC) neurons are the path along which GAP-43 reaches VCN; (4) partial cochlear lesions induce the emergence of GAP-43 positive presynaptic endings only in regions tonotopically corresponding to the extent of the lesion; (5) judging from the presence of immature fibers and growth cones in VCN on the deafened side, at least part of the GAP-43 positive presynaptic endings appear to be newly formed neuronal contacts following axonal sprouting while others may be modified pre-existing contacts; and (6) GAP-43 positive synapses are formed only on specific postsynaptic profiles, i.e., glutamatergic, glycinergic and calretinin containing cell bodies, but not GABAergic cell bodies. We conclude that unilateral deafening, be it partial or total, induces complex patterns of reconnecting neurons in the adult auditory brainstem, and we evaluate the possibility that the deafness-induced chain of events is optimized to remedy the loss of a bilaterally balanced activity in the auditory brainstem.


Asunto(s)
Vías Auditivas/fisiología , Núcleo Coclear/metabolismo , Proteína GAP-43/metabolismo , Pérdida Auditiva Unilateral/fisiopatología , Plasticidad Neuronal/fisiología , Animales , Nervio Coclear/lesiones , Núcleo Coclear/ultraestructura , Lateralidad Funcional , Proteína GAP-43/genética , Inmunohistoquímica , Hibridación in Situ , Degeneración Nerviosa , Neuronas/metabolismo , Ruido/efectos adversos , Núcleo Olivar , ARN Mensajero/metabolismo , Ratas , Ratas Wistar
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