INTRODUÇÃO: Este estudo tem como objetivo comparar os achados biomecânicos e anatomopatológicos de um modelo animal inédito de tendinopatia do tendão do calcâneo, induzido por injeções seriadas de baixa dose da enzima colagenase bacteriana, com o modelo mais comumente utilizado na literatura, induzido por injeção única de maior dose da enzima, e com os controles. A hipótese é que a utilização de injeções seriadas resultaria em alterações tendíneas mais progressivas e duradouras, similar à doença nos humanos. MÉTODOS: Quarenta e cinco (N=45) coelhos foram randomizados em três diferentes grupos de estudo (A, B e Controles). Animais do Grupo A (n=18) foram submetidos a três injeções seriadas de baixa dose de colagenase (0,1mg), em ambos os tendões do calcâneo, separadas por intervalo de duas semanas. Animais do Grupo B (n=18) foram injetados com dose única de maior dose (0,3mg). Já no Grupo Controle, animais (n=9) foram injetados bilateralmente com três doses seriadas de solução fisiológica 0,9%. Após a última injeção, foi realizada eutanásia do mesmo número de animais dos Grupos A e B (n=6), com 10 semanas (Subgrupos A1 e B1), 12 semanas (Subgrupos A2 e B2) e 16 semanas (Subgrupos A3 e B3). Todos os animais do Grupo controle foram eutanasiados após 16 semanas. Alterações anatomopatológicas, pelo escore de Bonar, e biomecânicas foram comparadas entre os grupos e dentro de cada grupo, para os diferentes momentos de eutanásia. Valores de p < 0,05 foram considerados estatisticamente significativos. RESULTADOS: Após 16 semanas, o escore anatomopatológico de Bonar foi significativamente maior para ambos os Grupos A (11,8±2,28) e B (5,6±2,51), quando comparados aos controles (2±0,76). Os valores para o grupo A também diferiram do Grupo B (p < 0,001). Para os desfechos biomecânicos, os grupos diferiram quanto à área de secção transversa do tendão (p=0,003), módulo de elasticidade (p=0,024), e tensões no limite da elasticidade (p=0,020) e na resistência máxima (p=0,022), com piores resultados encontrados nos animais do Grupo A. Na semana 12, também houve diferença entre os Grupos A e B para o escore anatomopatológico de Bonar (p=0,028) e para a tensão no limite da elasticidade(p=0,013), novamente com piores resultados no Grupo A. Já na 10a semana, foram os coelhos do Grupo B que demonstraram alterações mais pronunciadas quando comparados aos do Grupo A, com diferença significativa no Escore de Bonar (p=0,033), área de secção transversa do tendão (p=0,038), rigidez (p=0,048), módulo de elasticidade (p=0,024), força, tensão, energia e densidade de energia no limite da elasticidade (p=0,008, p=0,020, p=0,047 e p=0,0015, respectivamente) além de força e tensão no limite da resistência máxima (p=0,004 e p=0,008, respectivamente). A comparação dos desfechos dentro de cada grupo, entre os diferentes subgrupos, apresentou diferenças significativas no escore de Bonar em ambos os grupos A (p=0,012) e B (p < 0,001). Parâmetros biomecânicos não diferiram entre os subgrupos do Grupo A. Já os subgrupos do grupo B apresentaram diferenças na área de secção transversa do tendão (p=0,011), módulo de elasticidade (p=0,024), tensão no limite da elasticidade (p=0,023) e da resistência máxima (p=0,031), assim como na a densidade de energia no limite da elasticidade (p=0,017), com resultados mais pronunciados no subgrupo B1. CONCLUSÃO: O modelo animal de tendinopatia do tendão calcâneo induzida por injeções seriadas de colagenase apresentou alterações anatomopatológicas e biomecânicas mais avançadas na 16a semana, de caráter progressivo e duradouro, similar à doença dos humanos. Tal modelo experimental pode representar uma melhor opção na indução da tendinopatia do tendão do calcâneo, possibilitando a realização de estudos promissores no futuro / INTRODUCTION: This study aims to compare the biomechanical and histological findings of a new animal model of Achilles tendinopathy induced by serial low-dose injections of bacterial collagenase with the most commonly used high-dose single injection and to controls. The hypothesis of the study is that consecutive low-dose injections of collagenase would result in more progressive and long-lasting tendinopathic findings, reproducing better the disease in humans. METHODS: Forty-five (N=45) rabbits were randomly divided into three groups (A, B and Control). Animals in Group A (n=18) underwent three serial low-dose (0,1mg) injections of bacterial type I collagenase in both Achilles tendons, separated by a two-week interval. Animals in Group B (n=18) underwent bilateral single high dose injection (0,3mg) of the same enzyme. In the Control Group, animals (n=9) were injected bilaterally with three consecutive doses of saline solution, separated by a two-week interval. Following the last injection, the same number of rabbits from Groups A and B (n=6) were euthanized after 10 weeks (Subgroups A1 and B1), 12 weeks (Subgroups A2 and B2), and 16 weeks (Subgroups A3 and B3). Animals in the Control Group were all euthanized after 16 weeks. Histological findings, using the Bonar tendinopathy score, and biomechanical properties of the Achilles tendons were compared between the groups and inside each the group, in the different time-points of euthanasia. Findings at 16 weeks were considered primary outcomes. P-values < 0,05 were considered significant. RESULTS: After 16 weeks, the Bonar score was significantly increased for both Groups A (11,8±2,28) and B (5,6±2,51), when compared to controls (2±0,76). Group A has also differed from Group B (p < 0,001). Regarding biomechanical findings, groups differed in cross-sectional area of the Achilles tendon (p=0,003), Young\'s modulus (p=0,024), Yield stress (p=0,020) and ultimate tensile strength (p=0,022), with the worst results in animals from Group A. At 12 weeks, comparison between Groups A and B have shown significant differences for Bonar score (p=0,028) and Yield stress (p=0,013), again with worse results in Group A. Conversely, at 10 weeks, rabbits in Group B showed worse results when compared to Group A, with significant differences in the Bonar score (p=0,033), cross sectional area of the tendon (p=0,038), stiffness (p=0,048), Young\'s modulus (p=0,024), Yield tension (0,008), Yield stress (p=0,020), energy Yield (p=0,047), ultimate tension (p=0,004), ultimate stress (p=0,008) and yield strain energy density (p=0,015). The comparison of outcomes inside each group, in the different time-points of follow-up, demonstrated significant differences in the Bonar score for Group A (p=0,012) and Group B (p < 0,001). Regarding biomechanical properties, Group A showed no differences between the subgroups for any of the parameters evaluated. Subgroups in Group B differed for cross-sectional area of the tendon (p=0,011), Young\'s modulus (p=0,024), Yield stress (p=0,023), ultimate stress (p=0,031) and yield strain energy density (p=0,017), with worst results in the earliest follow-up (Subgroup B1). CONCLUSIONS: The animal model of Achilles tendinopathy induced by consecutive injections of collagenase showed worse histological and biomechanical properties after 16 weeks, demonstrating more progressive and long lasting tendinopathic findings, reproducing better the disease in humans. This novel experimental model can represent a better option to induce Achilles tendinopathy, allowing promising future research on the subject

A direct bone tendon junction consists of four zones: tendon, uncalcified fibrocartilage, calcified fibrocartilage, and bone. The uncalcified and calcified fibrocartilage together forms the transition zone. This organization ensures a gradual transition in stiffness and material properties, and protects the junction from failure. Transition zone regeneration during bone tendon junction healing is important to restore this unique protective mechanism. / Bone tendon junction repair is involved in many orthopaedic reconstructive procedures. Healing is observed to be slow. The junction often heals by fibrous tissue formation. Previous attempts to enhance bone tendon junction healing have resulted in increased bone formation. However, fibrocartilage transition zone is not restored. / This thesis describes a series of studies on transition zone regeneration in bone tendon junction healing using two partial patellectomy animal models. The healing process inside a bone trough was first studied and characterized. Little transition zone regeneration was observed except near the articular cartilage cut surface. The possibility of using articular cartilage to stimulate transition zone regeneration was explored. Both articular cartilage autograft and allogeneic cultured chondrocyte pellet implantations resulted in significantly increased fibrocartilage transition zone regeneration. Cell tracking indicated that the regenerated tissue likely originated from host cells. To elucidate the mechanism of stimulation by allogeneic cultured chondrocyte pellet, the role of cellular and matrix component needed to be differentiated. Freezing and rapid freeze thaw cycles permanently devitalized the allogeneic cultured chondrocyte pellet, but retained its structural integrity and matrix contents. Preliminary results indicated that implantation of the devitalized allogeneic cultured chondrocyte pellet could still increase fibrocartilage transition zone regeneration. Cellular activity seemed not to be essential for the stimulatory effect. / With further research and development, it is envisioned that a cartilage-based stimulation method for fibrocartilage transition zone regeneration in bone tendon junction healing will be developed for clinical application. / Wong Wan Nar, Margaret. / Source: Dissertation Abstracts International, Volume: 70-06, Section: B, page: 3423. / Thesis (M.D.)--Chinese University of Hong Kong, 2008. / Includes bibliographical references (leaves 216-231). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstracts in English and Chinese. / School code: 1307.

INTRODUÇÃO: Este estudo tem como objetivo comparar os achados biomecânicos e anatomopatológicos de um modelo animal inédito de tendinopatia do tendão do calcâneo, induzido por injeções seriadas de baixa dose da enzima colagenase bacteriana, com o modelo mais comumente utilizado na literatura, induzido por injeção única de maior dose da enzima, e com os controles. A hipótese é que a utilização de injeções seriadas resultaria em alterações tendíneas mais progressivas e duradouras, similar à doença nos humanos. MÉTODOS: Quarenta e cinco (N=45) coelhos foram randomizados em três diferentes grupos de estudo (A, B e Controles). Animais do Grupo A (n=18) foram submetidos a três injeções seriadas de baixa dose de colagenase (0,1mg), em ambos os tendões do calcâneo, separadas por intervalo de duas semanas. Animais do Grupo B (n=18) foram injetados com dose única de maior dose (0,3mg). Já no Grupo Controle, animais (n=9) foram injetados bilateralmente com três doses seriadas de solução fisiológica 0,9%. Após a última injeção, foi realizada eutanásia do mesmo número de animais dos Grupos A e B (n=6), com 10 semanas (Subgrupos A1 e B1), 12 semanas (Subgrupos A2 e B2) e 16 semanas (Subgrupos A3 e B3). Todos os animais do Grupo controle foram eutanasiados após 16 semanas. Alterações anatomopatológicas, pelo escore de Bonar, e biomecânicas foram comparadas entre os grupos e dentro de cada grupo, para os diferentes momentos de eutanásia. Valores de p < 0,05 foram considerados estatisticamente significativos. RESULTADOS: Após 16 semanas, o escore anatomopatológico de Bonar foi significativamente maior para ambos os Grupos A (11,8±2,28) e B (5,6±2,51), quando comparados aos controles (2±0,76). Os valores para o grupo A também diferiram do Grupo B (p < 0,001). Para os desfechos biomecânicos, os grupos diferiram quanto à área de secção transversa do tendão (p=0,003), módulo de elasticidade (p=0,024), e tensões no limite da elasticidade (p=0,020) e na resistência máxima (p=0,022), com piores resultados encontrados nos animais do Grupo A. Na semana 12, também houve diferença entre os Grupos A e B para o escore anatomopatológico de Bonar (p=0,028) e para a tensão no limite da elasticidade(p=0,013), novamente com piores resultados no Grupo A. Já na 10a semana, foram os coelhos do Grupo B que demonstraram alterações mais pronunciadas quando comparados aos do Grupo A, com diferença significativa no Escore de Bonar (p=0,033), área de secção transversa do tendão (p=0,038), rigidez (p=0,048), módulo de elasticidade (p=0,024), força, tensão, energia e densidade de energia no limite da elasticidade (p=0,008, p=0,020, p=0,047 e p=0,0015, respectivamente) além de força e tensão no limite da resistência máxima (p=0,004 e p=0,008, respectivamente). A comparação dos desfechos dentro de cada grupo, entre os diferentes subgrupos, apresentou diferenças significativas no escore de Bonar em ambos os grupos A (p=0,012) e B (p < 0,001). Parâmetros biomecânicos não diferiram entre os subgrupos do Grupo A. Já os subgrupos do grupo B apresentaram diferenças na área de secção transversa do tendão (p=0,011), módulo de elasticidade (p=0,024), tensão no limite da elasticidade (p=0,023) e da resistência máxima (p=0,031), assim como na a densidade de energia no limite da elasticidade (p=0,017), com resultados mais pronunciados no subgrupo B1. CONCLUSÃO: O modelo animal de tendinopatia do tendão calcâneo induzida por injeções seriadas de colagenase apresentou alterações anatomopatológicas e biomecânicas mais avançadas na 16a semana, de caráter progressivo e duradouro, similar à doença dos humanos. Tal modelo experimental pode representar uma melhor opção na indução da tendinopatia do tendão do calcâneo, possibilitando a realização de estudos promissores no futuro / INTRODUCTION: This study aims to compare the biomechanical and histological findings of a new animal model of Achilles tendinopathy induced by serial low-dose injections of bacterial collagenase with the most commonly used high-dose single injection and to controls. The hypothesis of the study is that consecutive low-dose injections of collagenase would result in more progressive and long-lasting tendinopathic findings, reproducing better the disease in humans. METHODS: Forty-five (N=45) rabbits were randomly divided into three groups (A, B and Control). Animals in Group A (n=18) underwent three serial low-dose (0,1mg) injections of bacterial type I collagenase in both Achilles tendons, separated by a two-week interval. Animals in Group B (n=18) underwent bilateral single high dose injection (0,3mg) of the same enzyme. In the Control Group, animals (n=9) were injected bilaterally with three consecutive doses of saline solution, separated by a two-week interval. Following the last injection, the same number of rabbits from Groups A and B (n=6) were euthanized after 10 weeks (Subgroups A1 and B1), 12 weeks (Subgroups A2 and B2), and 16 weeks (Subgroups A3 and B3). Animals in the Control Group were all euthanized after 16 weeks. Histological findings, using the Bonar tendinopathy score, and biomechanical properties of the Achilles tendons were compared between the groups and inside each the group, in the different time-points of euthanasia. Findings at 16 weeks were considered primary outcomes. P-values < 0,05 were considered significant. RESULTS: After 16 weeks, the Bonar score was significantly increased for both Groups A (11,8±2,28) and B (5,6±2,51), when compared to controls (2±0,76). Group A has also differed from Group B (p < 0,001). Regarding biomechanical findings, groups differed in cross-sectional area of the Achilles tendon (p=0,003), Young\'s modulus (p=0,024), Yield stress (p=0,020) and ultimate tensile strength (p=0,022), with the worst results in animals from Group A. At 12 weeks, comparison between Groups A and B have shown significant differences for Bonar score (p=0,028) and Yield stress (p=0,013), again with worse results in Group A. Conversely, at 10 weeks, rabbits in Group B showed worse results when compared to Group A, with significant differences in the Bonar score (p=0,033), cross sectional area of the tendon (p=0,038), stiffness (p=0,048), Young\'s modulus (p=0,024), Yield tension (0,008), Yield stress (p=0,020), energy Yield (p=0,047), ultimate tension (p=0,004), ultimate stress (p=0,008) and yield strain energy density (p=0,015). The comparison of outcomes inside each group, in the different time-points of follow-up, demonstrated significant differences in the Bonar score for Group A (p=0,012) and Group B (p < 0,001). Regarding biomechanical properties, Group A showed no differences between the subgroups for any of the parameters evaluated. Subgroups in Group B differed for cross-sectional area of the tendon (p=0,011), Young\'s modulus (p=0,024), Yield stress (p=0,023), ultimate stress (p=0,031) and yield strain energy density (p=0,017), with worst results in the earliest follow-up (Subgroup B1). CONCLUSIONS: The animal model of Achilles tendinopathy induced by consecutive injections of collagenase showed worse histological and biomechanical properties after 16 weeks, demonstrating more progressive and long lasting tendinopathic findings, reproducing better the disease in humans. This novel experimental model can represent a better option to induce Achilles tendinopathy, allowing promising future research on the subject

Magnetic Resonance Imaging (MRI) is an imaging modality that acquires an image with little to no damage to the tissue. MRI does not introduce foreign particles or high energy radiation into the body, making it one of the least invasive medical imaging modalities. MRI can achieve excellent soft tissue contrast and is therefore useful for diagnosis of a wide variety of diseases. While there are a wide variety of available techniques for generating contrast in MRI, there are still many open areas for research. For example, many tissues in the human body exhibit such rapid signal decay that they are difficult to image with MRI: they are "MRI invisible". Furthermore, some of the newer MRI imaging techniques have not been fully validated to ensure that they are truly revealing accurate information about the underlying anatomical microstructure that they purport to image. This dissertation focuses on the development of new techniques in two distinct areas. First, a novel method for accurately assessing the MRI signal decay properties of tissues that are normally MRI invisible, such as tendons, ligaments, and certain pathological chemical deposits in the brain, is presented. This is termed "ultrashort MRI relaxometry". Second, two new image processing algorithms that operate on high resolution images of stained histological slices of the ex vivo brain are presented. The first of these image processing algorithms allows the semi-automated extraction of nerve fiber directionality from the histological slice images, a process that is normally done manually, is incredibly time consuming, and is prone to human error. This new technique represents one significant step in the complicated problem of attempting to validate a popular MRI technique, Diffusion Tensor Imaging (DTI), by ensuring that DTI results correlate with the true underlying physiology revealed by histological slicing and staining. The second of these image processing algorithms attempts to extract and segment regions of different "cytoarchitectonic characteristics" from stained histological slices of ex vivo brain. Again, traditional cytoarchitectonic segmentation relies on manual segmentation by an expert neuroanatomist, which is slow and sometimes inconsistent. The new technique is a first step towards automated this process, potentially providing greater accuracy and repeatability of the segmentations in a much shorter time. Together, these contributions represent a significant contribution to the body of MR imaging techniques, and associated image processing techniques for validation of newer MR neuroimaging techniques against the gold standard of stained histological slices of ex vivo brain.

Dans un contexte de performance sportive, de réhabilitation ou de santé, les étirements sont couramment utilisés dans le but de préparer le système neuromusculaire à l’exercice subséquent. Si la littérature montre majoritairement que les étirements altèrent de façon aigue la performance musculaire et/ou fonctionnelle, il existe toutefois des études dont les résultats diffèrent, suggérant l’influence d’un certain nombre de facteurs sur la variabilité des réponses du système neuromusculaire. Pour une meilleure compréhension de cette variabilité et des mécanismes impliqués, cette thèse avait pour objectif d’examiner l’influence de différents paramètres sur le système neuromusculaire : la durée d’étirement, le groupe musculaire et la modalité d’étirement. Au travers de quatre études, il a été montré que les étirements statiques pouvaient altérer la production de force maximale et les propriétés neuromusculaires indépendamment de la durée d’étirement. Cependant, il est apparu que ces modulations étaient spécifiques au muscle, et plus précisément à la raideur relative du système musculo-tendineux. Indépendamment de la durée d’étirement, les étirements statiques ne seraient pas efficaces pour préparer le système neuromusculaire à une activité musculaire subséquente, et notamment pour des muscles raides. Plus particulièrement, les étirements dynamiques ne paraissent pas plus efficaces. Même si les effets néfastes ont été diminués comparativement aux étirements statiques, ils ne favoriseraient pas davantage la production de force ni la commande nerveuse. Toutefois, il est intéressant de noter qu’une durée courte d’étirements dynamiques peut réduire la résistance passive à l’étirement, et donc augmenter potentiellement l’amplitude articulaire maximale, sans affecter les capacités de production de force. Finalement, les étirements dynamiques pourraient être envisagés comme une activité musculaire dynamique, qui compense partiellement les effets néfastes de l’étirement sur la performance musculaire. D’un point de vue pratique, ceci suggère que ce type d’étirements peut être réalisé avant une performance, mais néanmoins accompagnés d’une activité musculaire de plus haute intensité, afin d’optimiser les effets de l’échauffement musculaire sur le système neuromusculaire. En définitive, la variabilité des réponses du système neuromusculaire serait dépendante de facteurs spécifiques, tels que la modalité d’étirement et la raideur relative du système musculo-tendineux, soulignant l’importance de les prendre en considération dans la pratique. / Stretching is traditionally incorporated into pre-exercise routines in health, rehabilitation and sporting environments to condition the neuromuscular system for exercise. While a large body of evidence reported that stretching may acutely impair the subsequent muscular performance, some conflicting results highlight possible mitigating factors of neuromuscular responses variability. Because the limited data available do not present a clear consensus, the aim of this thesis was to investigate the effects of different factors on neuromuscular responses to stretch: the muscle group, the stretch duration and modality. By means of four studies, it has been shown that static stretching may alter maximal voluntary torque and neuromuscular properties, irrespective of the stretch duration. However, these modulations were dependent on the muscle group, and more specifically on the intrinsic stiffness of the muscle-tendon system. Regardless of the stretch duration, static stretching appears to be not effective, or even detrimental, to prepare the musculotendinous system for subsequent exercises, and especially for stiff muscles. It is also relevant that dynamic stretching was not better than static stretching. Even if stretch-induced impairments were mitigated compared to static stretching, dynamic stretching would not optimize muscle strength capacities and central nervous system. However, a short duration of dynamic stretching may be sufficient to reduce passive resistive torque, and therefore potentially increase maximal range of motion, without affecting muscle strength capacities. Finally, dynamic stretching could be considered as dynamic muscle activity, which would partly counteract deleterious muscle-tendon stretching effects. From a practical point of view, dynamic stretching could be a part of warm-up procedure, but should be associated to stronger contractions to optimize the improvement in muscle strength capacities. In summary, the variability of neuromuscular responses to stretch would be dependent on specific factors, such as stretching modality and relative stiffness of the musculotendinous system, emphasizing the importance of taking it into consideration in practice.

La corrosion dans le béton précontraint est considérée parmi les pathologies les plus dangereuses dans le secteur du génie civil. En effet ce phénomène se caractérise par la gravité de ses conséquences économiques et sécuritaires. L’objectif de ce travail consiste à évaluer l’efficacité d’un inhibiteur à base de phosphates Na3PO4.12H2O contre la corrosion des aciers de précontrainte. L’étude a été d’abord menée en milieu synthétique simulant le béton chloruré sur des armatures tendues à 80% Rm, puis d’une part sur des éprouvettes en mortier précontraint conçues à l’échelle laboratoire, et d’autre part en utilisant la technique de cellule de diffusion pour tester l’efficacité de l’inhibiteur à long terme. Les résultats issus de l’étude réalisée dans le milieu simulant ont révélé que la présence des phosphates entraine l’augmentation du seuil critique d’amorçage de corrosion localisée R=[Cl-]/[OH-] jusqu’à la valeur de 5 au lieu de 0,4. Ceci semble être dû à deux actions inhibitrices des phosphates à savoir : la stabilisation de la couche protectrice à base d’oxyde de fer et la formation de composés phosphatés très peu solubles qui bloquent les sites anodiques actifs, augmentant ainsi la résistance de l’acier à la corrosion localisée. L’emploi de Na3PO4.12H2O en tant qu’adjuvant diminue légèrement la résistance à la compression du mortier. Cependant les composés phosphatés provenant de la réaction de l’inhibiteur avec les hydrates de ciment colmatent les pores du mortier et freinent la diffusion des chlorures. Ceci améliore le comportement à la corrosion des armatures enrobées de mortier précontraint. Enfin, lorsque le triphosphate de sodium est utilisé comme inhibiteur migrateur ou comme moyen de prétraitement des armatures, la technique de la cellule de diffusion a montré son efficacité à long terme, grâce à l’augmentation de la période précédant l’amorçage d’une corrosion localisée, où l’armature est en état passif. / Corrosion in prestressed concrete is considered among the most dangerous pathologies in the civil engineering sector. Indeed, this phenomenon is characterized by the seriousness of its economic and security consequences. The objective of this work is to evaluate the efficiency of a phosphate based inhibitor Na3PO4.12H2O against the corrosion of prestressing steels. The study was first conducted on wires tensioned at 80% Rm and immersed in simulating concrete pore solution. Then it concerned, on one hand, prestressed mortar specimens designed on a laboratory scale and, on the other hand, the long term efficiency of the inhibitor using diffusion cell technique. The results obtained from the study carried out in the concrete simulating medium revealed that the presence of the phosphates causes the increase in the critical threshold of localized corrosion initiation R = [Cl -] / [OH-] up to the value of 5 instead of 0.4. This seems to be due to two phosphate inhibiting actions, namely: the stabilization of the iron oxide protective layer and the formation of very insoluble phosphate compounds which block the active anodic sites, increasing prestressing steel resistance to localized corrosion. The use of Na3PO4.12H2O as an additive slightly reduces the compressive strength of the mortar. However, phosphate compounds resulting from the reaction of the inhibitor with the cement hydrates clog the pores of the mortar and slow down the diffusion of the chlorides. This improves the corrosion behavior of prestressed mortar reinforcement. Finally, when sodium triphosphate is used as a migratory inhibitor or as a means of steel reinforcement pretreatment, the diffusion cell technique has shown its long-term efficiency, thanks to the increase of the period preceding the initiation of a localized corrosion, where the reinforcement is in a passive state.

Bei jugendlichen Athleten wirken sowohl die körperliche Reifung als auch die erhöhte mechanische Belastung auf die Entwicklung des Muskel- und Sehnengewebes. Die Interaktion dieser beiden adaptationswirksamen Stimuli könnte, insbesondere bei Sportlern aus Sprungdisziplinen, Dysbalancen des Kraftpotenzials der Muskulatur und der Widerstandsfähigkeit der Sehne auslösen und somit potentiell das Verletzungsrisiko der Sehne erhöhen. Vor diesem Hintergrund untersucht die vorliegende Arbeit mittels Magnetresonanztomographie, Ultraschall und Dynamometrie die Entwicklung der morphologischen und mechanischen Eigenschaften der Knieextensoren und der Patellarsehne bei jugendlichen Kader-Volleyballathleten. Durch eine Querschnitts- und zwei Längsschnittstudien konnte Evidenz dafür erbracht werden, dass sich unter dem Einfluss der sportartspezifischen Belastung Kraft und Morphologie des Muskels in Relation zu den mechano-morphologischen Eigenschaften der Patellarsehne bei den jugendlichen Athleten nicht ausgewogen entwickeln, was zu einer erhöhten chronischen Belastung und Beanspruchung des Sehnengewebes führt. Darüber hinaus können muskulotendinöse Dysbalancen im Trainingsprozess durch erhöhte Fluktuationen der Muskelkraft und einer nicht-adäquaten Modulation der Widerstandsfähigkeit der Sehne zu episodischen Spitzen der mechanischen Beanspruchung der Sehne führen. Eine derart unausgewogene Entwicklung von Muskel und Sehne könnte für die Ausprägung von Überlastungsbeschwerden in der hier untersuchten Risikogruppe für Tendinopathien prädisponieren. Im Rahmen der Forschungsbemühungen wurde darüber hinaus ein Verfahren zur Vorhersage des Volumens von Oberschenkelmuskeln auf der Basis einfach zu erhebender Parameter entwickelt. Durch das Verfahren ließe sich zukünftig der Zeit- und Kostenaufwand muskelmorphologischer Diagnostik deutlich reduzieren. / In adolescent athletes, the development of muscle and tendon tissue is influenced both by maturation and mechanical loading. The interaction of these two driving stimuli could initiate imbalances in the development of the muscle strength capacity and tendon stiffness, especially in athletes from sports that feature a high frequency of jumps. A consequence could be an increased mechanical demand placed upon the tendon by the working muscle, which might increase the risk of tendon injury. Considering the lack of information on the effects of maturation and superimposed mechanical loading on the muscle-tendon unit during adolescence, the present work examines the development of the morphological and mechanical properties of the knee extensors and patellar tendon in adolescent elite volleyball athletes by means of magnetic resonance imaging, ultrasound and dynamometry. A cross-sectional comparison and two longitudinal studies provided evidence that the two-fold stimulus of sport-specific loading and maturation results in and imbalanced development of muscle strength and morphology in relation to the mechano-morphological properties of the patellar tendon in mid-adolescent volleyball athletes and results in increased tendon stress and strain. Moreover, during a training process, fluctuations of muscle strength and an inadequate modulation of tendon stiffness initiate episodes of high-level tendon strain during maximum muscle contractions. Such an imbalanced development of muscle and tendon could predispose for the development of tendon overuse injury in adolescent volleyball athletes, which are known to be at high risk of developing tendinopathy. Moreover, in the context of the described research endeavour, a method for the volume prediction of thigh muscles on the basis of easily measurable parameters has been developed, which could greatly reduce the time and costs involved in the diagnostics of muscle morphology in the future.

Die klinischen Langzeitergebnisse des vorderen Kreuzbandersatz mit dem Patellarsehnentransplantat nach durchschnittlich 13,8 Jahren waren nicht zufriedenstellend. Hauptursachen hierfür waren operativ-technische Mängel, wie Fehlpositionierung der Bohrkanäle und die Fixierung der Transplantate in einer zu hohen Kniebeugestellung. Diese Abweichungen führten zu signifikant schlechteren Bewegungsausmaßen sowohl in der Streckung als auch in der Beugung. Insbesondere bei zu weit ventral positionierter femoraler Bohrkanalanlage resultierte ein erhebliches Beugedefizit mit Stressbelastung auf das femorotibiale Kompartiment, ähnlich einem Nußknackerphänomen. Bei zu weit ventral positioniertem tibialen Bohrkanal wurde eine signifikante Verringerung der Extension beobachtet. Die Patienten mit gleichzeitiger Meniskusresektion hatten signifikant höhere arthrotische Veränderungen. Sowohl die zum damaligen Zeitpunkt allgemein anerkannte Operationstechnik als auch die postoperative Rehabilitation ist zeitlich überholt und entspricht nicht den gegenwärtigen internationalen Standards. In der experimentellen Untersuchung zum Einwachsverhalten einer autologen vorderen Kreuzbandplastik am Kaninchenmodell konnte der Einfluss und die Wirkung von manipulativ wirkenden Faktoren auf die Ausbildung eines stabilen Bindegewebsregenerates belegt werden. Sowohl der fibrinstabilisierende Faktor XIII als auch die eingesetzte Transplantat-Splitting-Technik zeigten eine positive Wirkung auf den Ein- und Umbau sowie den biomechanischen Ausrissfestigkeiten der Transplantate. Die alleinige Wirkung des Faktor XIII spielt vor allem in der Frühphase eine stimulierende Rolle auf die Initiierung der Umbauvorgänge und der ossären Intergration der Knochenblöcke. Mittel- und langfristig wird die Ausbildung von belastungsstabilen Kollagenfibrillen durch andere weitestgehend unbekannte Einflussfaktoren bestimmt. Die neuartig entwickelte Transplantat-Splitting-Technik erwies sich für den Transplantatumbau ebenfalls als vorteilhaft. Mit dieser Transplantatbearbeitung wurde die Grundlage für eine frühzeitige synoviale Ernährung der Bündel gewährleistet. Durch die artifizielle Gewebsläsion werden reparative Vorgänge beschleunigt. Auf der Grundlage der experimentell gewonnenen Daten kann die Transplantat-Splitting- Technik für die klinische Erprobung und Praxiseinführung empfohlen werden. / The clinical long term results mean 13,8 years after anterior cruciate ligament reconstructions with bone-patellar tendon-bone transplant were not satisfied. Main reasons were technical errors, malpositioning of the bone tunnels and fixation of the transplant in a too high degree of flexion. As a result the patients had significant reductions of motion in extension as well as in flexion. Especially in cases with an anterior femoral bone tunnel position the patients had a loss of flexion and high degree of shear forces in the femoro-tibial compartment similar a nutcracker phenomenon. In ACL reconstructions with an anterior tibial bone tunnel position could be observed a loss of extension. Patients with concomitant meniscal resection showed significant higher rate of osteoarthrotic changes. Both, the former operative technique and the postoperative rehabilitation programme had no clinical relevance today and are replaced by new standards. In an experimental study regarding to the remodeling process of an autologous anterior cruciate ligament plasty in a rabbit model could be examined factors which influencing the maturation process of the graft. The fibrin stabilizing factor XIII as well as the transplant splitting technique showed a positive effect in the remodelling process and the pull-out strength of the transplants. In the early phase the factor XIII activated the initial remodeling and the osseous ingrowth of the bone blocks. In middle and long term period of remodeling there plays unknown factors an important role for building of force restraint collagen fibrils. The new developed splitting technique had some additional advantages. Using these technique the basis of early synovial nutrition could be realized. The artificial tissue lesion leads to an acceleration of the reparative response. On the basis of the experimental data the transplant splitting technique can be recommended and introduce in the clinical trial.

For small diameter (<6 mm) blood vessel replacements, lack of collaterals and vascular disease preclude homografts; while synthetic analogs, ePTFE, expanded polytetrafluoroethylene, and PET, polyethyleneterephathalate, are prone to acute thrombosis and restenosis. It is postulated that the hierarchical assembly of cell populated matrices fabricated from protein analogs provides a new design strategy for generating a structurally viable tissue engineered vascular graft. To this end, synthetic elastin and collagen fiber analogs offer a novel strategy for creating tissue engineered vascular grafts with mechanical and biological properties that match or exceed those of native vessels. This work details techniques developed for the fabrication of prosthetic vascular grafts from a series of extracellular matrix analogs composed of nanofibrous collagen matrices and elastin-mimetic proteins, with and without cells, and subsequent evaluation of their biocompatibility and mechanical properties. The work details the fabrication and mechanical analysis of vascular grafts made from aforementioned protein analogs. Subesequent studies detail seeding and proliferation of rodent mesenchymal stem cells on protein-based composites to recapitulate the media of native vasculature. Finally detailing in vivo biocompatibility and stability of tissue engineered vascular grafts.

The interface between tendon/ligament and bone tissue is a complex transition of biochemical, cellular, and mechanical properties. Investigating computational and tissue engineering models that imitate aspects of this interface may supply critical design parameters for designing future tissue replacements to promote increased biochemical and mechanical integration between tendon/ligament and bone. Strategies for modeling this tissue have typically focused on the development of heterogeneous structures to create gradients or multiphasic materials that mimic aspects of the transition. However, further work is required to elucidate the role of specific mechanical and material stimuli in recapitulating features of the tendon/ligament-bone insertion. In particular, in constructs that exhibit variation in both mechanical and biochemical properties, the interplay of mechanical, material, and chemical signals can complicate understanding of the particular factors at work in interface formation. Thus, the overall goal of this dissertation was to provide insight into the role of mechanical strain and scaffold degradability on cell behavior within heterogeneous biomaterials. Specifically, a method for determining cell vertical position within a degradable gel through a laminated interface was developed. A computational model was created to examine possible variation in local mechanical strain due to heterogeneity in mechanical properties and different interface geometries. Finally, the influence of biomaterial degradability on changes in encapsulated human mesenchymal stem cell morphology under response to cyclic mechanical strain was explored. Together, these studies provide insight into mechanical and material design considerations when devising tissue engineering strategies to regenerate the tendon/ligament-bone interface.