Foi realizado um estudo experimental da influência do ultra-som terapêutico na regeneração do nervo ciático submetido a esmagamento controlado, em ratos. Foram empregados no estudo 20 ratos da linhagem Wistar, de peso médio em torno de 250 g, divididos em dois grupos, conforme o tipo de procedimento realizado: 1) somente esmagamento, dez ratos; e 2) esmagamento e irradiação com ultra-som, 10 ratos. Sob anestesia, o nervo ciático era exposto na coxa direita do animal e esmagado com um dispositivo especialmente idealizado e confeccionado para essa finalidade, com uma carga fixa de 15 Kg, por 10 minutos, num segmento de 5 mm proximal à sua bifurcação. A irradiação com o ultra-som pulsado (1:5, freqüência de 1 MHz, intensidade de 0.4 W/'CM POT.2', duração de 2 minutos) era iniciada já no primeiro dia pós-operatório e realizada por dez dias consecutivos. Os resultados foram avaliados pela análise funcional da impressão plantar dos animais obtidas numa pista de marcha e determinação do índice funcional do ciático (De Medinaceli e Bain, Mackinnon e Hunter), e pela morfometria, através do cálculo da densidade de fibras nervosas, após sacrifício dos animais no vigésimo primeiro dia pós-operatório. Os resultados foram submetidos a análise estatística e mostraram que, nas condições do trabalho, o ultra-som acelerou a regeneração do nervo, demonstrável com significância no vigésimo primeiro dia pós-operatório / An experimental study of the influence of therapeutic ultrasound on the regeneration of the sciatic nerve submitted to controlled crush injury was carried out in rats. Twenty female Wistar rats weighing 250 g on average were used and distributed in two groups according to the procedure: 1) crush injury only, ten rats; 2) crush injury followed by ultrasound irradiation, ten rats. Under general anesthesia the sciatic nerve was exposed on the right thigh and crushed with a device especially devised and built for that purpose, with a 15 kg constant load for 10 minutes, affecting a 5 mm-long segment of the nerve proximal to its bifurcation. Pulsed ultrasound irradiation (1:5, 1 MHz frequency, 0.4 W/'CM POT.2' intensity, 2 minutes duration) was started the day after the operation and repeated for ten consecutive days. The results were evaluated by functional footprint analysis and determination of the sciatic functional index (DeMedinaceli's and Bain, Mackinnon and Hunter's methods) at weekly intervals, and by morphometry (nerve fiber density) of the resected sciatic nerve after killing the animals on the 21st postoperative day. Results were submitted to statistical evaluation and showed that, in the conditions of the study, ultrasound accelerated nerve regeneration, as demonstrated with significance on the 21st postoperative day

Peripheral nerve injuries occur with high incidence and often result in profound and permanent impact on the life of patients and on healthcare expenditure. Schwann cells (SC) play a promoting role in peripheral nerve regeneration providing physical and neurotrophic support that aids axon re-growth. However, these beneficial properties are not exploitable in nerve tissue engineering due to the difficulties in SC harvesting and expansion in culture. Adult stem cells derived from bone marrow (BM-MSC) and from adipose tissue (ASC) can be differentiated in SC-like cells and be used as SC substitutes in bioengineered nerve conduits for the improvement of peripheral nerve regeneration. Pharmacological intervention approaches for the treatment of nerve injury are still not clinically available. Nevertheless, γ-Aminobutyric acid (GABA) receptors have been recently suggested as a putative target for such purpose. GABA is the main inhibitory neurotransmitter of the adult brain and interacts with two different receptor types. However, both GABA-A and GABA-B receptor types are functionally expressed also in SC, where they are involved in the regulation of SC physiology and in the development of the peripheral nervous system (PNS).The aim of this thesis was to characterise the GABAergic system of BM-MSC and ASC differentiated into a SC-like phenotype and to evaluate changes in the expression levels following differentiation. Moreover, the effect of specific GABA receptor ligands on cell proliferation and neurotrophic potential of differentiated stem cells were assessed. Using reverse transcriptase polymerase chain reaction, western blot analysis and immunohistochemistry we demonstrated that adult stem cells express several subunits of both GABA-A and GABA-B receptor systems such as GABA-B1a, GABA-B1b and GABA-B2, as well as GABA-A α2 and GABA-A β3. Expression levels and cellular localisation were comparable with adult and neonatal SC cultures used as positive controls, and protein expression levels for some of the subunits changed following glial differentiation. Interestingly, stimulation of GABA receptors with specific agonists influenced stem cell proliferation in two opposite ways. Baclofen, a GABA-B receptor agonist decreased proliferation of SC and differentiated ASC (dASC), but not of SC-like BM-MSC (dBM-MSC). By contrast, muscimol, a GABA-A receptor agonist, increased proliferation in SC and in both dASC and dBM-MSC. This suggests that GABAergic signalling could be a potential player in the mechanisms regulating stem cell differentiation and proliferation as reported in SC. Finally, baclofen treatments on SC and dASC modulated the expression levels and the release of the neurotrophins BDNF and NGF, which are key actors in the processes involved with peripheral nerve regeneration. Although further studies will be needed to clarify the role of GABA receptors in the PNS, the presence of functional GABA receptors on SC-like adult stem cells could represent an exploitable pharmacological target to modulate stem cell physiology and improve their neurotrophic potential for peripheral nerve regeneration.

Foi realizado um estudo experimental da influência do ultra-som terapêutico na regeneração do nervo ciático submetido a esmagamento controlado, em ratos. Foram empregados no estudo 20 ratos da linhagem Wistar, de peso médio em torno de 250 g, divididos em dois grupos, conforme o tipo de procedimento realizado: 1) somente esmagamento, dez ratos; e 2) esmagamento e irradiação com ultra-som, 10 ratos. Sob anestesia, o nervo ciático era exposto na coxa direita do animal e esmagado com um dispositivo especialmente idealizado e confeccionado para essa finalidade, com uma carga fixa de 15 Kg, por 10 minutos, num segmento de 5 mm proximal à sua bifurcação. A irradiação com o ultra-som pulsado (1:5, freqüência de 1 MHz, intensidade de 0.4 W/'CM POT.2', duração de 2 minutos) era iniciada já no primeiro dia pós-operatório e realizada por dez dias consecutivos. Os resultados foram avaliados pela análise funcional da impressão plantar dos animais obtidas numa pista de marcha e determinação do índice funcional do ciático (De Medinaceli e Bain, Mackinnon e Hunter), e pela morfometria, através do cálculo da densidade de fibras nervosas, após sacrifício dos animais no vigésimo primeiro dia pós-operatório. Os resultados foram submetidos a análise estatística e mostraram que, nas condições do trabalho, o ultra-som acelerou a regeneração do nervo, demonstrável com significância no vigésimo primeiro dia pós-operatório / An experimental study of the influence of therapeutic ultrasound on the regeneration of the sciatic nerve submitted to controlled crush injury was carried out in rats. Twenty female Wistar rats weighing 250 g on average were used and distributed in two groups according to the procedure: 1) crush injury only, ten rats; 2) crush injury followed by ultrasound irradiation, ten rats. Under general anesthesia the sciatic nerve was exposed on the right thigh and crushed with a device especially devised and built for that purpose, with a 15 kg constant load for 10 minutes, affecting a 5 mm-long segment of the nerve proximal to its bifurcation. Pulsed ultrasound irradiation (1:5, 1 MHz frequency, 0.4 W/'CM POT.2' intensity, 2 minutes duration) was started the day after the operation and repeated for ten consecutive days. The results were evaluated by functional footprint analysis and determination of the sciatic functional index (DeMedinaceli's and Bain, Mackinnon and Hunter's methods) at weekly intervals, and by morphometry (nerve fiber density) of the resected sciatic nerve after killing the animals on the 21st postoperative day. Results were submitted to statistical evaluation and showed that, in the conditions of the study, ultrasound accelerated nerve regeneration, as demonstrated with significance on the 21st postoperative day

Objectifs: Hepatocyte Growth Factor (HGF) améliore la régénération axonale et la survie des motoneurones lors du développement embryonnaire. Son rôle dans la régénération des nerfs périphériques lésés chez l’adulte n’a pas encore été étudié. Notre objectif est de déterminer l’expression de HGF dans la moelle épinière murine suite à une axotomie, avec ou sans stimulation électrique, directe ou transcutanée. Méthodes: Soixante souris C57BL/6 adultes ont été divisées en 5 groupes : Contrôle (n=12), Placebo (n=12), Axotomie (n=12, lacération et réparation immédiate du nerf sciatique), Directe (n=12, lacération, réparation immédiate et stimulation électrique directe proximale du nerf sciatique, 1h, 20 Hz) et Transcutanée (n=12, lacération, réparation immédiate et stimulation électrique transcutanée proximale du nerf sciatique, 1h, 20 Hz). Les moelles épinières ont été recueillies 1, 3, 7 et 14 jours suivant l’intervention. L’expression de HGF a été évaluée par technique d’hybridation in situ. Résultats: Nos résultats démontrent une augmentation de l’expression de HGF dans les moelles épinières murines suite à l’axotomie. Cette augmentation est plus rapide suite à la stimulation électrique, autant directe que transcutanée. L’expression de HGF devient localisée aux zones motrices de la moelle épinière murine dans les groupes Axotomie, Directe et Transcutanée. Conclusions: HGF, facteur neurotrophique impliqué de le développement et la survie des motoneurones, a une expression altérée suite à la lacération du nerf sciatique. Ceci suggère fortement qu’il participe aussi à la régénération des nerfs moteurs. De plus, l’expression plus rapide de HGF suite à la stimulation électrique suggère son implication dans l’augmentation de la régénération nerveuse. / Purpose: Hepatocyte Growth Factor (HGF) plays a role in promoting axonal growth and survival of motoneurons during embryonic development. This factor might also be important in directing the regeneration of adult motoneurons following laceration. We aim to identify the expression patterns of HGF following axotomy, with or without direct or transcutaneous electrical nerve stimulation in a mouse model. Methods: Sixty adult C57BL/6 mice were divided into 5 groups: Control (n=12), Sham (n=12), Axotomy (n=12, sciatic nerve laceration and immediate repair), Direct (n=12, sciatic nerve laceration, immediate repair and application of direct electrical stimulation on the proximal nerve end, 1h, 20 Hz) and Transcutaneous (n=12, nerve laceration and immediate repair followed by proximal transcutaneous electrical stimulation, 1h, 20 Hz). Spinal cords were harvested at 1, 3, 7 and 14 days post-surgery. The expression patterns of HGF were measured using in situ hybridization. Results: Our results showed an upregulation of HGF expression in mouse spinal cords following sciatic nerve axotomy. This occurred more quickly following electrical stimulation in both Direct and Transcutaneous groups. The expression pattern of HGF became localized to the motor neuron pools in the Axotomy, Direct and Transcutaneous groups. Conclusions: HGF, a growth factor involved in directing the outgrowth of motor axons in development, has an altered expression pattern following sciatic nerve laceration, suggesting it may also play a role in directing motoneuron regeneration. Furthermore, rapid change in the expression pattern of HGF following electrical stimulation suggests it may also be involved in the upregulation of nerve regeneration following electrical stimulation.

Introduction : Les conduits nerveux synthétiques représentent une alternative chirurgicale aux autogreffes dans la réparation des traumatismes aux nerfs périphériques. Afin d’améliorer la régénération nerveuse périphérique, plusieurs biomatériels, tels que la multicouche polyélectrolyte de soie (MPE), et modèles ont été étudiés. Dans le cadre de ma maitrise, nos objectifs de recherche sont d’établir si la MPE de soie permet d’améliorer la régénération nerveuse périphérique in vivo et si notre nouveau modèle de conduit (« jelly roll ») peut mener à une meilleure régénération du nerf sciatique chez le rat que le modèle de conduit creux. Méthodes : Dans cette étude, une technique chirurgicale in vivo de lacération et de réparation du nerf sciatique chez le rat fut utilisé. Cinq conditions expérimentales de conduits (autogreffe, conduit creux avec et sans MPE de soie et « jelly roll » avec et sans MPE de soie) furent implantées (n= 2 rats par condition). Après 4 semaines, les conduits furent récupérés et marqués par immunohistochimie avec le neurofilament et la protéine basique de la myéline (MBP). La performance de chaque conduit fut évaluée par sa capacité à supporter l’excroissance axonale à travers le long du conduit et à travers la largeur de ce dernier à divers endroits. Résultats : Chaque condition expérimentale a supporté une régénération axonale avec différents degrés de succès. Globalement, l’autogreffe a supporté une plus longue croissance de fibres. De plus, la surface de fibres obtenue était plus large que les autres conditions. Les conduits avec la MPE de soie ont eu une performance similaire à leurs homologues sans soie. De plus, le modèle de conduit creux a mené à une meilleure régénération axonale que le modèle du « jelly roll ». Conclusion : L’autogreffe demeure le meilleur conduit pour supporter la régénération nerveuse périphérique. Les conduits avec la MPE de soie peuvent supporter une régénération nerveuse similaire aux conduits sans soie tandis que le modèle de « jelly roll » a généré des performances inférieures au modèle de conduit creux. / Background: Synthetic nerve conduits constitute alternative surgical options to autografts in the repair of peripheral nerve injuries. Silk polyelectrolyte multilayer (PEM) as a biomaterial and novel conduit designs have been proposed to improve peripheral nerve regeneration. In my master’s project, my objective is to assess whether silk PEM can improve peripheral nerve regeneration in vivo and to assess whether our novel conduit design (“jelly roll”) can better support rat sciatic nerve regeneration than a hollow conduit design. Methods: In this study, an in vivo rat model of sciatic nerve laceration and repair was used. Five experimental conduit conditions (autograft, hollow conduit with and without silk PEM, and jelly roll with and without silk PEM) were implanted (n=2 rats per condition). After 4 weeks, the conduits were harvested and immuno-stained for neurofilament and myelin basic protein (MBP). Conduit performance was assessed by its ability to support axonal outgrowth throughout the conduit’s length and at various locations along its width. Results: Each condition supported axonal regeneration at varying levels of success. Overall, the autograft group outperformed all other groups by supporting the longest and widest occupying regenerating fibers. Conduits with silk PEM performed similarly to conduits without silk PEM. In addition, the hollow conduit design demonstrated better regenerative outcomes than the jelly roll design. Conclusion: The autograft remains the superior conduit to support peripheral nerve regeneration. Conduits with silk PEM support nerve regeneration in the same capacity as non silk-coated conduits while the jelly roll design underperformed in comparison to the hollow conduit design.