Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Arán Pascual-Font is active.

Publication


Featured researches published by Arán Pascual-Font.


Muscle & Nerve | 2010

Topographical distribution of motor fascicles in the sciatic-tibial nerve of the rat

Jordi Badia; Arán Pascual-Font; Meritxell Vivó; Esther Udina; Xavier Navarro

Knowledge of the intraneural topography of peripheral nerves may help to improve nerve repair after injuries and the selectivity of neural interfaces. We studied the fascicular pattern of motor fibers of the rat sciatic–tibial nerve. We carried out an anatomical dissection of the muscular tributaries of the tibial nerve in the leg. Immunohistochemistry against choline acetyltransferase was used to identify motor axons. Retrograde tracing allowed localization of the muscular fascicles at proximal levels of the sciatic trunk. The distribution of motor fibers in transverse section of the tibial nerve is not homogeneous; two clusters were identified, each one containing fibers of functionally related muscles. Retrograde tracing allowed for the identification of motor fascicles, each one well localized along the sciatic nerve. In the rat there is a somatotopic organization of the sciatic nerve, with muscular fascicles maintaining the same relative position along the entire nerve. Muscle Nerve, 2010


IEEE Transactions on Biomedical Engineering | 2011

Biocompatibility of Chronically Implanted Transverse Intrafascicular Multichannel Electrode (TIME) in the Rat Sciatic Nerve

Jordi Badia; Tim Boretius; Arán Pascual-Font; Esther Udina; Thomas Stieglitz; Xavier Navarro

The transverse intrafascicular multichannel electrode (TIME) is intended to be transversally implanted in the peripheral nerve and to selectively interface subsets of axons in different fascicles within the same nerve. Two versions of TIME (TIME-2 and TIME-3) were designed and tested for biocompatibility and safety in the sciatic nerve of the rat. TIME-2 was implanted in two groups: the first group had only an acute implant and the second group had chronic implantation for two months; a third group was also chronically implanted with the TIME-3 version, designed to avoid the mechanical traction produced by muscles motion. We evaluated the functional and morphological effects of either TIME-2 or TIME-3 implanted in the rat sciatic nerve for two months. The results of the study indicate that implantation of the TIME-2 and TIME-3 devices in the nerve did not cause significant axonal loss or demyelination, as evidenced by the functional and histological results. The results of this study indicate that the TIME-2 and TIME-3 designs are biocompatible and safe after chronic implantation in a small peripheral nerve, such as the rat sciatic nerve.


Journal of Neurotrauma | 2011

Sigma receptor agonist 2-(4-morpholinethyl)1 phenylcyclohexanecarboxylate (Pre084) increases GDNF and BiP expression and promotes neuroprotection after root avulsion injury

Clara Penas; Arán Pascual-Font; Renzo Mancuso; Joaquim Forés; Caty Casas; Xavier Navarro

Spinal root avulsion leads to a progressive loss of axotomized motoneurons (MNs). Nowadays, there is no effective treatment to prolong MN survival that could permit recovery as a result of delayed surgical repair. Administration of Sigma-1 receptor (Sig-1R) ligands has been reported to promote beneficial effects after several types of neural injury. In order to shed light of whether Sig-1R ligands could promote MN survival after root avulsion, L4-L5 spinal roots were unilaterally avulsed in adult rats and the Sig-1R agonist Pre084 was administered at different doses. The ventral spinal cords of the animals were studied from 3 to 21 days post-operation (DPO) by using histological, immunohistochemical, and Western blot techniques. Daily treatment with 0.25 mg/kg Pre084 significantly promoted MN survival (68% vs 43% in untreated rats) at 21 DPO, an effect that was antagonized by coadministration of BD1063, an antagonist of Sig-1R. There was a reduction in astroglial- associated immunoreactivity in rats treated with Pre084. Moreover, Pre084 produced an increase in the Sig-1R co-chaperone BiP within MNs, and an increase of GDNF expression by astrocytes in the ventral horn early after injury. Although the mechanisms promoting MN survival by Pre084 remain unclear, we hypothesize that it is mediated at least in part through the increase in these cytoprotective factors. Therefore, early application of Sig-1R agonist appears to be a promising therapy to improve MN survival after root avulsion.


Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 2012

Recurrent laryngeal nerve landmarks revisited

Elham Asgharpour; Eva Maranillo; J. R. Sañudo; Arán Pascual-Font; Marc Rodriguez-Niedenführ; Francisco J. Valderrama; Fermin Viejo; Ian G. Parkin; Teresa Vázquez

The aim of this work was to evaluate, to prove their reliability, the different surgical landmarks previously proposed as a mean to locate the recurrent laryngeal nerve (RLN).


Journal of Anatomy | 2011

The central projections of the laryngeal nerves in the rat.

Arán Pascual-Font; Ignacio Hernández-Morato; Stephen McHanwell; Teresa Vázquez; Eva Maranillo; J. R. Sañudo; Francisco J. Valderrama-Canales

The larynx serves respiratory, protective, and phonatory functions. The motor and sensory innervation to the larynx controlling these functions is provided by the superior laryngeal nerve (SLN) and the recurrent laryngeal nerve (RLN). Classical studies state that the SLN innervates the cricothyroid muscle and provides sensory innervation to the supraglottic cavity, whereas the RLN supplies motor innervation to the remaining intrinsic laryngeal muscles and sensory innervation to the infraglottic cavity, but recent data suggest a more complex anatomical and functional organisation. The current neuroanatomical tracing study was undertaken to provide a comprehensive description of the central brainstem connections of the axons within the SLN and the RLN, including those neurons that innervate the larynx. The study has been carried out in 41 adult male Sprague–Dawley rats. The central projections of the laryngeal nerves were labelled following application of biotinylated dextran amines onto the SLN, the RLN or both. The most remarkable result of the study is that in the rat the RLN does not contain any afferent axons from the larynx, in contrast to the pattern observed in many other species including man. The RLN supplied only special visceromotor innervation to the intrinsic muscles of the larynx from motoneurons in the nucleus ambiguus (Amb). All the afferent axons innervating the larynx are contained within the SLN, and reach the nucleus of the solitary tract. The SLN also contained secretomotor efferents originating from motoneurons in the dorsal motor nucleus of the vagus, and special visceral efferent fibres from the Amb. In conclusion, the present study shows that in the rat the innervation of the larynx differs in significant ways from that described in other species.


Laryngoscope | 2011

Functional role of human laryngeal nerve connections.

Carlos Martín‐Oviedo; Eva Maranillo; Alejandro Lowy‐Benoliel; Arán Pascual-Font; Tomas Martínez-Guirado; Marc Rodriguez-Niedenführ; J. R. Sañudo; Bartolome Scola; Teresa Vázquez

Current knowledge of the functional role of human laryngeal nerves is based on traditional laryngeal neuroanatomic descriptions or contradictory electromyographic studies. The aim of this study was to clarify the functional role of neural connections between laryngeal nerves by correlating the different electromyographic patterns observed after laryngeal stimulation and the existence of different neural connections.


Journal of Anatomy | 2013

Reorganization of laryngeal motoneurons after crush injury in the recurrent laryngeal nerve of the rat

Ignacio Hernández-Morato; Francisco J. Valderrama-Canales; Gabriel Berdugo; Gonzalo Arias; Stephen McHanwell; J. R. Sañudo; Teresa Vázquez; Arán Pascual-Font

Motoneurons innervating laryngeal muscles are located in the nucleus ambiguus (Amb), but there is no general agreement on the somatotopic representation and even less is known on how an injury in the recurrent laryngeal nerve (RLN) affects this pattern. This study analyzes the normal somatotopy of those motoneurons and describes its changes over time after a crush injury to the RLN. In the control group (control group 1, n = 9 rats), the posterior cricoarytenoid (PCA) and thyroarytenoid (TA) muscles were injected with cholera toxin‐B. In the experimental groups the left RLN of each animal was crushed with a fine tip forceps and, after several survival periods (1, 2, 4, 8, 12 weeks; minimum six rats per time), the PCA and TA muscles were injected as described above. After each surgery, the motility of the vocal folds was evaluated. Additional control experiments were performed; the second control experiment (control group 2, n = 6 rats) was performed labeling the TA and PCA immediately prior to the section of the superior laryngeal nerve (SLN), in order to eliminate the possibility of accidental labeling of the cricothyroid (CT) muscle by spread from the injection site. The third control group (control group 3, n = 5 rats) was included to determine if there is some sprouting from the SLN into the territories of the RLN after a crush of this last nerve. One week after the crush injury of the RLN, the PCA and TA muscles were injected immediately before the section of the SLN. The results show that a single population of neurons represents each muscle with the PCA in the most rostral position followed caudalwards by the TA. One week post‐RLN injury, both the somatotopy and the number of labeled motoneurons changed, where the labeled neurons were distributed randomly; in addition, an area of topographical overlap of the two populations was observed and vocal fold mobility was lost. In the rest of the survival periods, the overlapping area is larger, but the movement of the vocal folds tends to recover. After 12 weeks of survival, the disorganization within the Amb is the largest, but the number of motoneurons is similar to control, and all animals recovered the movement of the left vocal fold. Our additional controls indicate that no tracer spread to the CT muscle occurred, and that many of the labeled motoneurons from the PCA after 1 week post‐RLN injury correspond to motoneurons whose axons travel in the SLN. Therefore, it seems that after RLN injury there is a collateral sprouting and collateral innervation. Although the somatotopic organization of the Amb is lost after a crush injury of the RLN and does not recover in the times studied here, the movement of the vocal folds as well as the number of neurons that supply the TA and the PCA muscles recovered within 8 weeks, indicating that the central nervous system of the rat has a great capacity of plasticity.


Anatomical Record-advances in Integrative Anatomy and Evolutionary Biology | 2013

Somatotopy of the Neurons Innervating the Cricothyroid, Posterior Cricoarytenoid, and Thyroarytenoid Muscles of the Rat's Larynx

Ignacio Hernández-Morato; Arán Pascual-Font; Carlos Ramírez; Jorge Matarranz-Echeverría; Stephen McHanwell; Teresa Vázquez; J. R. Sañudo; Francisco J. Valderrama-Canales

Neurons innervating the intrinsic muscles of the larynx are located within the nucleus ambiguus but the precise distribution of the neurons for each muscle is still a matter for debate. The purpose of this study was to finely determine the position and the number of the neurons innervating the intrinsic laryngeal muscles cricothyroid, posterior cricoarytenoid, and thyroarytenoid in the rat. The study was carried out in a total of 28 Sprague Dawley rats. The B subunit of the cholera toxin was employed as a retrograde tracer to determine the locations, within the nucleus ambiguus, of the neurons of these intrinsic laryngeal muscles following intramuscular injection. The labelled neurons were found ipsilaterally in the nucleus ambiguus grouped in discrete populations with reproducible rostrocaudal and dorsoventral locations among the sample of animals. Neurons innervating the cricothyroid muscle were located the most rostral of the three populations, neurons innervating the posterior cricoarytenoid were found more caudal, though there was a region of rostrocaudal overlap between these two populations. The most caudal were the neurons innervating the thyroarytenoid muscle, presenting a variable degree of overlap with the posterior cricoarytenoid muscle. The mean number (±SD) of labelled neurons was found to be 41 ± 9 for the cricothyroid, 39 ± 10 for the posterior cricoarytenoid and 33 ± 12 for the thyroarytenoid. Anat Rec, 296:470–479, 2013.


Acta otorrinolaringológica española | 2006

Proyecciones centrales del nervio laríngeo recurrente de la rata

Arán Pascual-Font; Eva Maranillo; A. Merchán; Teresa Vázquez; J. R. Sañudo; F.J. Valderrama Canales

Resumen Los nervios laringeos contienen las fibras que controlan la funcion laringea. Pocos y discrepantes son los estudios que se han realizado en la rata para conocer los componentes funcionales y el origen real de las fibras que componen el nervio laringeo recurrente (NLR). En ninguno de estos estudios se ha utilizado dextranos, potentes herramientas para el trazado nervioso. El objetivo de nuestro estudio es identificar en la rata los nucleos de origen de las fibras que porta el NLR, conociendo asi los componentes funcionales del mismo, mediante el trazado con dextranos biotinados (BDA). El estudio se ha realizado en 31 ratas Sprague-Dawley machos adultos, aplicando el BDA en el NLR previamente lesionado. Los resultados en todos los animales muestran que el NLR de la rata no ontiene fibras aferentes, mientras que las fibras eferentes se originan en el nucleo ambiguo (NA) ipsilateral. Por lo tanto, en la rata, el NLR parece contener exclusivamente fibras eferentes, debiendo de ser las fibras aferentes conducidas, muy probablemente en su totalidad, por el nervio laringeo superior.


Acta otorrinolaringológica española | 2006

Morfometría de los nervios laríngeos recurrentes de la rata

Arán Pascual-Font; A. Merchán; Eva Maranillo; A. Brillas; J. R. Sañudo; F.J. Valderrama Canales

Resumen Los nervios laringeos recurrentes (NLR) de los mamiferos son diferentes en longitud entre ambos lados. Esta asimetria implica, a priori, diferentes tiempos de conduccion del estimulo a la musculatura laringea controlada por cada nervio, postulandose diversos modelos para explicar el cierre glotico sincronico mas alla de la citada diferencia. Varios son los estudios publicados en esta materia aunque, no obstante, presentan carencias en datos relevantes. Utilizando dos grupos de 10 y 6 ratas, respectivamente, nuestro estudio compara la longitud de los NLR por lado y, mediante microscopia optica acoplada a un sistema de analisis morfometrico, el numero y caracteristicas de las fibras mielinicas que los componen. Los resultados muestran que el NLR izquierdo (NLRi) es, de promedio, 0,84 cm mas largo que el NLR derecho (NLRd). No hay diferencias estadisticamente significativas en el numero de fibras por lado pero si en el grosor de las mismas, mayors en el NLRd. Estos datos se analizan valorando los posibles mecanismos de compensacion de la diferencia de longitud de los NLR.

Collaboration


Dive into the Arán Pascual-Font's collaboration.

Top Co-Authors

Avatar

Teresa Vázquez

Complutense University of Madrid

View shared research outputs
Top Co-Authors

Avatar

J. R. Sañudo

Complutense University of Madrid

View shared research outputs
Top Co-Authors

Avatar

Eva Maranillo

Complutense University of Madrid

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Xavier Navarro

Autonomous University of Barcelona

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Jordi Badia

Autonomous University of Barcelona

View shared research outputs
Top Co-Authors

Avatar

Marc Rodriguez-Niedenführ

Complutense University of Madrid

View shared research outputs
Top Co-Authors

Avatar

A. Merchán

Complutense University of Madrid

View shared research outputs
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge