This project addresses characterization of the material properties of aortic tissue. Understanding of these properties is important for a variety of studies including tissue engineering, effects of aging and diseases, stents engineering, and traumatic aorta rupture. The goal of the presented research was to characterize the stress-strain relationship of aorta in dynamic oscillatory biaxial loading. A setup was developed that supplied pressure loading from the physiological to sub-failure levels (between 7 and 76 kPa) to porcine aorta at frequencies ranging from 0.50Hz to 5.00Hz. Samples tested were constrained at both ends while the deformation and the pressure were recorded. Volumetric strain versus pressure was used to characterize the structural behavior of the material which showed frequency dependency and hysteresis indicating viscoelastic response. An offset method was developed to account for drifting behavior exhibited by some of the samples. The structural behavior of aorta was modeled using a quasi-linear viscoelastic (QLV) creep theory. The QLV model included a logarithmic steady state elastic function v = 0.663 +/- 0.040 + 0.241 +/- 0.011 ln(P) for pressure in kPa, and a Prony series creep function ( J0 = 0.472 +/- 0.021, J2 = 0.109 +/- 0.060, J3 = 0.419 +/- 0.056). Modeling results were then used to determine the relationships between the circumferential and longitudinal stresses and strains of the material. The results exhibited that the stress in the transverse direction was about 1.5 times larger than in the axial direction. However, in the axial direction material was stiffer and the deformation was 30% less. The relaxation function of the material was determined by linearizing the non-linear component of the QLV model and applying to it the linear viscoelastic theory. Furthermore, literature comparison revealed that aorta's creep function, as well as its elastic modulus, is within the range of what has been reported in the literature. In conclusion, an experimental model was developed that can be used to predict the behavior of porcine aorta under physiological and sub-failure conditions at quasi-static and dynamic loading. / Mechanical Engineering

No / Tunica adventitia, the outer layer of blood vessels, is an important structural feature, predominantly consisting of collagen fibrils. This study uses pseudostatic atomic force microscopy (AFM) nanoindentation at physiological conditions to show that the distribution of indentation modulus and viscous creep for the tunica adventitia of porcine aorta and pulmonary artery are distinct. Dynamic nanoindentation demonstrates that the viscous dissipation of the tunica adventitia of the aorta is greater than the pulmonary artery. We suggest that this mechanical property of the aortic adventitia is functionally advantageous due to the higher blood pressure within this vessel during the cardiac cycle. The effects on pulsatile deformation and dissipative energy losses are discussed.

Abdominal aortic aneurysm (AAA) is characterized by a bulge in the abdominal aorta. AAA development is mostly asymptomatic, but such a bulge may suddenly rupture, which is associated with a high mortality rate. Unfortunately, there is no medication that can prevent AAA from expanding or rupturing. Therefore, patients with detected AAA are monitored until treatment indication, such as maximum AAA diameter of 55 mm or expansion rate of 1 cm/year. Models of AAA development may help to understand the disease progression and to inform decision-making on a patient-specific basis. AAA growth and remodeling (G&amp;R) models are rather complex, and before the challenge is undertaken, sound clinical validation is required. In Paper A, an existing thick-walled model of growth and remodeling of one layer of an AAA slice has been extended to a two-layered model, which better reflects the layered structure of the vessel wall. A parameter study was performed to investigate the influence of mechanical properties and G&amp;R parameters of such a model on the aneurysm growth. In Paper B, the model from Paper A was extended to an organ level model of AAA growth. Furthermore, the model was incorporated into a Fluid-Solid-Growth (FSG) framework. A patient-specific geometry of the abdominal aorta is used to illustrate the model capabilities. In Paper C, the evolution of the patient-specific biomechanical characteristics of the AAA was investigated. Four patients with five to eight Computed Tomography-Angiography (CT-A) scans at different time points were analyzed. Several non-trivial statistical correlations were found between the analyzed parameters. In Paper D, the effect of different growth kinematics on AAA growth was investigated. The transverse isotropic in-thickness growth was the most suitable AAA growth assumption, while fully isotropic growth and transverse isotropic in-plane growth produced unrealistic results. In addition, modeling of the tissue volume change improved the wall thickness prediction, but still overestimated thinning of the wall during aneurysm expansion. / Bukaortaaneurysm (AAA) kännetecknas av en utbuktning hos aortaväggen i buken. Tillväxt av en AAA är oftast asymtomatisk, men en sådan utbuktning kan plö̈tsligt brista, vilket har hög dödlighet. Tyvärr finns det inga mediciner som kan förhindra AAA från att expandera eller brista. Patienter med upptä̈ckt AAA hålls därför under uppsikt tills operationskrav är uppnådda, såsom maximal AAA-diameter på 55 mm eller expansionstakt på 1 cm/år. Modeller för AAA-tillväxt kan bidra till att öka förståelsen för sjukdomsförloppet och till att förbättra beslutsunderlaget på en patientspecifik basis. AAA modeller för tillväxt och strukturförändring (G&amp;R) är ganska komplicerade och innan man tar sig an denna utmaning krävs de god klinisk validering. I Artikel A har en befintlig tjockväggig modell för tillväxt av ett skikt av en AAA-skiva utö̈kats till en två-skiktsmodell. Denna modell återspeglar bättre den skiktade strukturen hos kärlväggen. Genom en parameterstudie undersö̈ktes påverkan av mekaniska egenskaper och G&amp;R-parametrar hos en sådan modell för AAA-tillväxt. I Artikel B utvidgades modellen från Artikel A till en organnivå-modell för AAA-tillväxt. Vidare inkorporerades modellen i ett “Fluid–Solid–Growth” (FSG) ramverk. En patientspecifik geometri hos bukaortan användes för att illustrera möjligheterna med modellen. I Artikel C undersöktes utvecklingen av patientspecifika biomekaniska egenskaper hos AAA. Fyra patienter som skannats fem till åtta gånger med “Computed Tomography-Angiography” (CT-A) vid olika tillfällen analyserades. Flera icke triviala statistiska samband konstaterades mellan de analyserade parametrarna. I Artikel D undersöktes effekten av olika tillväxt-kinematik för AAA tillväxt. En modell med transversellt-isotrop-i-tjockleken-tillväxt var den bäst lämpade för AAA tillväxt, medans antagandet om fullt-isotrop-tillväxt och transversellt-isotrop-i-planet-tillväxt producerade orimliga resultat. Dessutom gav modellering av vävnadsvolymsförändring ett förbättrat väggtjockleks resultat men en fortsatt överskattning av väggförtunningen under AAA-expansionen. / <p>QC 20161201</p>

Introdução: Modelos experimentais em suíno são essenciais para pesquisa e treinamento em transplante de fígado. No entanto, este animal apresenta instabilidade hemodinâmica grave durante a fase anepática, exigindo um curto período anepático (não apropriado para fins de treinamento) ou o uso de circulação extracorpórea (que está associado a significativas complicações intra-operatórias). Além disso, a maioria dos modelos em suíno é alogênico, o que não é nem eticamente nem economicamente adequado para treinamento cirúrgico. Objetivo: Desenvolver e testar um modelo de autotransplante hepático em suínos sem o uso de circulação extracorpórea. Métodos: Onze porcos da raça Sus domesticus foram submetidos a cirurgia simulada (SHAM; n = 3) ou autotransplante de fígado (grupo experimental (GE); n = 8) sem o uso de circulação extracorpórea. Após a realização de uma incisão em \"J\", o hilo hepático foi inteiramente dissecado abaixo do nível da artéria gastroduodenal e o fígado completamente mobilizado. A aorta supracelíaca foi então dissecada através do pilar esquerdo do diafragma. Nenhuma outra etapa foi realizada no grupo SHAM. No GE, a partir de então, procedeu-se o autotransplante ortotópico de fígado empregando-se a técnica convencional com duas anastomoses de veia cava, semelhante à técnica clássica utilizada na prática clínica. Durante a fase anepática, foi utilizando o clampeamento da aorta supracelíaca a fim de manter a estabilidade hemodinâmica e evitar o uso do by-pass. Os animais foram submetidos a eutanásia 1h após o término do procedimento cirúrgico. Parâmetros hemodinâmicos e exames laboratoriais foram sistematicamente coletados em 4 tempos distintos: basal, pré-reperfusão, 5min após reperfusão e ao término do experimento. Foi realizada a análise histopatológica do enxerto após a reperfusão. A análise estatística foi feita comparando amostras relacionadas, no GE, e duas amostras independentes, entre os grupos. Resultados: Empregando a técnica por nós padronizada, obteve-se 100% de sobrevida dos animais, todos estáveis hemodinamicamente. Os tempos médios de observação pós-reperfusão e anepático foram de 136±12,50min e 47,88±8,03min, respectivamente. Não houve diferença estatística na pressão arterial média (PAM) entre o início e término do experimento no GE, nem entre os grupos durante a fase anepática. Ao término do experimento, a PAM foi significantemente maior no grupo SHAM quando comparado ao GE. A análise comparativa dos exames laboratoriais entre os grupos demonstrou que o pH, o bicarbonato e o base excess foram significantemente inferiores no GE 5min após a reperfusão e ao término do experimento. O lactato mostrou-se ser significantemente inferior ao término do experimento no grupo SHAM. Conclusão: De acordo com os métodos utilizados no presente estudo, desenvolveu-se um modelo de autotransplante de fígado em suínos sem a utilização de mecanismo de circulação extracorpórea. Para tanto, utilizou-se o clampeamento da aorta supracelíaca durante o período anepático. O modelo proposto é factível por cirurgiões em treinamento e com baixa mortalidade / Background: Experimental swine models have been essential for liver transplantation research and training. However, it experiences severe hemodynamic instability during the anhepatic phase, requiring either a short anhepatic phase (not appropriate for training purposes) or an extracorporeal circulation (which is linked to significant intraoperative complications). Furthermore, most of swine models are allograft ones, which is neither ethically nor financially suitable for surgical training. Objective: To develop and test a liver autotransplantation model in pig without venovenous bypass. Methods: Eleven Sus domesticus pigs underwent either sham surgery (SHAM group; n=3) or liver autotransplantation without venovenous bypass (experimental group (GE); n=8) by resident or fellow from Digestive Organs Transplant Division. After performing a rightsided J-shaped incision, hepatic hilum was entirely dissected under the level of the gastroduodenal artery and liver completely mobilized. Supraceliac aorta was then dissected through the diaphragm\'s left crus. No further step was performed in SHAM group. In the GE, thereafter, a liver autotransplantation was performed applying conventional bicaval anastomosis technique, similar to the classic technique used in clinical setting. During anhepatic phase, supraceliac aorta cross-clamping maneuver was carried out to sustain hemodynamic stability and avoid venovenous bypass. Animals underwent euthanasia one hour after the end of surgical procedure. Hemodynamic variables and blood samples were systematically collected at 4 different times: baseline, pre-reperfusion, 5min after reperfusion and at the end of experiment. Histological analysis of the graft was performed after reperfusion. Statistical analysis was accomplished comparing related samples in the GE and two independent samples between groups. Results: Applying the technique standardized by us, 100% survival was accomplished, all the animals hemodynamically stable. The mean post-reperfusion observation and anhepatic phase times were 136 ± 12.50 min and 48.38 ± 7.80 min, respectively. There was no statistical difference in mean arterial pressure (MAP) between baseline and the end of the experiment time in the GE, nor between the groups during the anhepatic phase. At the end of the experiment, MAP was significantly higher in the SHAM group compared to the experiment group. Blood samples statistical analysis between groups showed that pH, bicarbonate and base excess were significantly lower at 5 min post-reperfusion time and at the end of the experiment in the GE. The lactate was shown to be significantly lower in the SHAM group at the end of the experiment. Conclusion: According to the methods applied in the present study, a model of liver autotransplantation in swine was developed without the use of an extracorporeal circulation mechanism. For this purpose, supraceliac aortic cross-clamping maneuver was carried out during the anhepatic phase. The advocated model is feasible for training purpose with low mortality

Toxinas que atuam em canais para Na+ operados por voltagem são as principais responsáveis pelos efeitos tóxicos do envenenamento escorpiônico e podem ser divididas em duas classes: a- e b-neurotoxinas. TsTX-V e TsTX-I da peçonha de Tityus serrulatus (TsV) são, respectivamente, exemplos destas toxinas. Neste trabalho, foram avaliados os efeitos da TsV e destas toxinas sobre a pressão arterial média (PAM) e liberação de catecolaminas em ratos conscientes e não imobilizados, previamente cateterizados, bem como a captação de GABA, dopamina (DA) e glutamato (Glu) em sinaptosomas isolados de cérebro de ratos e a concentração citoplasmática de Ca+2 ([Ca+2 ]C) em células de músculo liso vascular de aorta de ratos. As toxinas foram isoladas por cromatografia de troca iônica (TsTX-I) seguida por CLAE de fase reversa (TsTX-V). As toxinas (15 e 30 g/kg) e TsV (50 e 100 g/kg) foram injetadas intravenosamente. A PAM foi monitorada continuamente através do cateter femoral. Os níveis plasmáticos de adrenalina (ADR) e noradrenalina (NA) foram determinados por CLAE de fase reversa com detector eletroquímico, em 10 min antes e 2,5, 30 e 90 min após os tratamentos. Efeitos pressores máximos foram observados em 2,5?3,5 min. TsV induziu um intenso aumento de longa duração na PAM, bem como a TsTX-I. A TsTX-V mostrou efeitos pressores menores. TsV mostrou os maiores efeitos sobre a liberação de catecolaminas, seguido pela TsTX-I e TsTX-V com um efeito máximo em 2,5 min, seguido por uma gradual redução, permanecendo, todavia, maior que os controles. Embora ambas as classes de toxinas atuem em canais para Na+, TsTX-I mostrou efeitos mais significantes e intensos sobre a liberação de catecolaminas e pressão arterial que a TsTX-V. Parece que a toxicidade da TsTX-V não está somente relacionada à sua capacidade de liberar catecolaminas, indicando que outros neutrotransmissores podem estar envolvidos em sua toxicidade. Nem a TsV ou suas toxinas foram capazes de afetar a captação de 3H-Glu. TsTXI inibiu somente a captação de 3H-DA (IC50 = 28,41 nM). Por outro lado, TsV (0,43ng/mL) inibiu a captação de 3H-GABA e 3H-DA (~50%). TsTX-V mostrou IC50 = 9,37 nM e 22,2 nM para a captação de 3H-GABA e 3HDA, respectivamente. Esses efeitos foram abolidos pelo pré-tratamento com TTX, indicando o envolvimento de canais para Na+ neste processo. Na ausência de Ca+2 e em baixas concentrações de toxinas, a redução não é tão singnificante como na presença de Ca+2. TsTX-V não reduziu a captação de 3H-GABA em células COS-7 expressando os transportadores de GABA, GAT-1 e GAT-3, sugerindo que esta toxina reduz indiretamente o transporte. A redução da captação de 3H-GABA pelos sinaptosomas pode ser devido a rápida e intensa despolarização celular, como revelado por microscopia confocal em células de glioma C6. Assim, TsTX-V causou redução da captação de 3H-GABA e 3H-DA de uma maneira independente de Ca+2, não afetando diretamente os transportadores de GABA, mas em consequencia da despolarização, envolvendo canais para Na+ operados por voltagem. TsV e suas toxinas foram capazes de aumentar a ([Ca2+ ]C , provavelmente por interargir com canais para Na+. Quando comparado aos efeitos despolarizantes do KCl 60 mM (100 %), TsV (100 e 500 g/mL) exibiu um aumento de 49,60 ± 2,58 % e 103,66 ± 5,17 %, respectivamente, enquanto que a TsTX-I e TsTX-V (50 e 100 g/mL de cada) exibiu 43,92 ± 3,06 % e 121,8 ± 8,9 %; 52,56 ± 8,33 % e 79,5 ± 6,1 % de aumento, respectivamente. TsTX-I (100 g/mL) mostrou-se mais potente nesta preparação, visto que uma dose de 100 g/mL causou efeito muito mais intenso do que a TsTX-V na mesma concentração. É possível que as diferenças observadas sobre os efeitos induzidos pela TsTX-I e TsTX-V sejam conseqüência de alterações estruturais entre canais para Na+ presentes em vários tipos de tecidos e inervações. / Voltage-gated Na+ channel toxins are mainly responsible for the toxic effects of scorpion envenoming and can be classified into two classes: a- and b-neurotoxins. TsTX-V and TsTX-I from Tityus serrulatus venom (TsV) are, respectively, examples of these toxins. In this work, were evaluate the effects of TsV and its toxins on mean arterial pressure (MAP) and catecholamines release in conscious unrestrained rats previously catheterized, as well as GABA, dopamine (DA) and glutamate (Glu) uptake in isolated rat brain synaptosomes and cytosolic Ca2+ concentration ([Ca2+ ]C) in vascular smooth muscle cells from rat aorta. Toxins were isolated by ion exchange chromatography (TsTX-I) followed by RP-HPLC (TsTX-V). The toxins (15 and 30 g/kg) and TsV (50 and 100 g/kg) were injected intravenously. MAP was continuously monitored through femoral catheter. Epinephrine (E) and norepinephrine (NE) plasma levels were determined by RP-HPLC with electrochemical detection, at 10 min before and 2.5, 30 and 90 min after treatments. Maximal pressor effects were observed at 2.5 3.5 min. TsV induced intense long lasting increase in MAP, as did TsTX-I. TsTX-V showed the lowest pressor effects. TsV showed the highest effects on catecholamines release, followed by TsTX-I and TsTX-V with maximal effect at 2.5 min, followed by a gradual reduction, however remaining higher than controls. Although both toxins act on Na+ channels, TsTX-I displayed significant and more intense effects on catecholamines release and blood pressure than TsTX-V. It seems that the toxicity of TsTX-V is not related only with its ability to release catecholamines, indicating that other neurotransmitters, may be involved in its toxicity. Neither the TsV or its toxins was capable to affect the 3H-Glu uptake. TsTX-I inhibited only 3H-DA uptake (IC50 = 28.41 nM). On the other hand, TsV (0.43ng/mL) inhibited both 3H-GABA and 3H-DA uptake (~50%). TsTX-V showed IC50 = 9.37 nM and 22.2 nM for 3H-GABA and 3H-DA uptake, respectively. These effects were abolished by pre-treatment with TTX, indicating the involvement of Na+ channels in this process. In the absence of Ca2+ and at low concentrations of toxin, the reduction is not as significant as in the presence of Ca2+. TsTX-V did not reduce 3H-GABA uptake in COS-7 cells expressing GABA transporters GAT-1 and GAT-3, suggesting that this toxin indirectly reduces the transport. The reduced 3H-GABA uptake by synaptosomes could be due to fast and intense cell depolarization as revealed by confocal microscopy of C6 glioma cells. Thus, TsTX-V causes reduction on 3H-GABA and 3H-DA uptake in a Ca2+-independent manner, not affecting directly GABA transporters, but, in consequence of depolarization, involving voltage-gated Na+ channels. TsV and its toxins were able to increase the ([Ca2+ ]C , probably by interact with Na+ channels. When compared to KCl 60 mM depolarizing effect (100 %), TsV (100 and 500 ?g/mL), showed an increase of 49.60 ± 2.58 % and 103.66 ± 5.17 %, respectively, whereas TsTX-I and TsTX-V (50 and 100?g/mL of each) showed 43.92 ± 3.06 % and 121.8 ± 8.9 %; 52.56 ± 8.33 % and 79.5 ± 6.1 %, respectively. TsTX-I (100 ?g/mL) showed most potent effects in this type of preparation, since induced most intense effect that TsTX-V in the same concentration. Thus, it is possible that the differences observed on the effects induced by both toxins are consequence of structural changes among Na+ channels present in several types of tissues and innervations .

O aneurisma de aorta abdominal (AAA) é uma doença assintomática na maioria dos casos, podendo acometer 5% das pessoas do gênero masculino com idade superior a 65 anos, predispondo ao risco de ruptura com mortalidade em torno de 80%. O presente estudo teve como objetivo avaliar os perfis de expressão gênica e de metilação do DNA no tecido, como também os microRNAs no plasma e no tecido de indivíduos com e sem AAA na tentativa de identificar marcadores biológicos e alvos terapêuticos para o diagnóstico, monitoramento e tratamento precoce do AAA. Os perfis de expressão gênica, miRNA e metilação de DNA dos tecidos da aorta abdominal (n=6) obtidos durante a cirurgia aberta para correção de AAA foram comparados com tecidos da aorta abdominal de doadores de órgãos sem AAA (n=6). Também foram comparados os perfis de miRNAs circulantes no plasma do grupo AAA (n=6) com o grupo-controle de voluntários com as características semelhantes, porém sem AAA (n=6). Para a análise da expressão gênica, utilizou-se a qPCR Array, analisando-se genes relacionados ao endotélio vascular humano (PAHS-015Z, QIAGEN®). A análise do perfil de miRNA foi realizada utilizando-se Human miFinder 384HC miScript miRNA PCR Array (MIHS-3001Z, QIAGEN®) e, para análise de metilação do DNA, utilizou-se a qPCR array com 22 genes das vias de estresse e toxicidade EpiTect Methyl II (EAHS-581Z, QIAGEN®). O software Ingenuity Pathway analysis (IPA®) foi utilizado para identificação das prováveis relações entre os microRNAs e a expressão gênica realizada nesta pesquisa. No estudo da expressão gênica, quatro genes (SPHK-1, TYMP, ALOX5 e HIF1A) foram identificados como mais expressos e outros 6 genes (PTGIS, CX3CL1, ITGB1, COL18A-1, FN1 e AGTR1) apresentaram expressão reduzida nos tecidos de AAA. Na análise do perfil de miRNAs, 24 miRNAs foram significantemente mais expressos e 35 miRNAs menos expressos no tecido. No plasma de indivíduos com AAA, 8 miRNAs apresentaram-se mais expressos e 9 miRNAs menos expressos. Dois miRNAs, miR-328-3p e let-7c-5p demonstraram expressões comuns entre tecido e plasma. Quanto ao padrão de metilação de DNA, somente o gene GDF15 teve grau de metilação maior nos tecidos de AAA quando comparado ao grupo-controle. A análise funcional revelou que o gene PTGIS (prostaciclina sintetase), um potente vasodilatador e inibidor da atividade plaquetária, foi reprimido pelo miR-150-5p, que se mostrou 7,5 vezes mais expresso no tecido de AAA, e teve uma possível interação com o miR-328-3p, cuja expressão foi 3,7 vezes mais baixa no tecido. Os genes com expressão reduzida nos tecidos do AAA foram alvos de miRNAs com expressão aumentada, evidenciando a importância e influência dos fatores epigenéticos tanto para o desenvolvimento quanto para a gravidade do AAA. / Abdominal aortic aneurism (AAA) is an asymptomatic disease in the majority of cases that may occur in 5% of males over age 65, predisposing to the risk of rupture leading to a mortality rate of 80%. The aim of this study was to evaluate the DNA metilation and gene expression profile in tissue, and microRNA expression pattern in both plasma and tissue samples from individuals with and without AAA to identify biological markers and therapeutic targets for an early diagnosis and treatment of AAA, respectively. Genes and miRNA expression and DNA metilation profiles in AAA tissues (n= 6) were compared to abdominal aortic tissues obtained from organ donators without AAA (n = 6). We also compared circulating miRNAs profiles in plasma samples, between AAA (n = 6) and the control group without AAA (n = 6). For the gene expression analysis we used a qPCR Array (PAHS-015Z, QIAGEN®) to analyze genes related to human vascular endothelium. For the miRNA expression pattern and for DNA methylation analysis we used the Human miFinder 384HC miScript miRNA PCR Array (MIHS-3001Z, QIAGEN®) and EpiTect Methyl II (EAHS-581Z, QIAGEN®), respectively. The Ingenuity software was used to identify the interactions between the miRNAs and genes evaluated in this study. Four genes (SPHK-1, TYMP, ALOX5 and HIF1A) were upregulated and six other genes (PTGIS, CX3CL1, ITGB1, COL18A-1, FN1 e AGTR1) were downregulated in AAA tissues. In addition, the miRNAs analysis showed 24 miRNAs more expressed and 35 miRNAs less expressed in AAA tissue than controls. Although in plasma samples, AAA group presented 8 miRNAs more expressed and 8 miRNAs less expressed than controls. Only, miR-328-3p and let-7c-5p were differently expressed between AAA and controls in both tissue and plasma samples. DNA methylation analysis showed that the gene GDF15 was hypermethylated in AAA tissues when compared to the control group. Functional analysis revealed that PTGIS, a potent vasodilator and platelet activity inhibitor was supressed by miR-150-5p, which had a seven-fold increase in AAA tissues. Moreover, a possible interaction between PTGIS and miR-328-3p, about 4-fold decreased in AAA tissues, was showed. Thus, the downregulated genes in AAA tissues are targets of miRNAs with increased expression in the same biological sample. These results highlight the importance and influence of epigenetic factors for both development and severity of AAA.

INTRODUÇÃO: A isquemia da medula espinhal continua sendo uma importante complicação nas cirurgias das doenças da aorta descendente torácica e toracoabdominal. OBJETIVOS: Células-tronco são capazes de promover a regeneração do tecido nervoso. Células-tronco derivadas do cordão umbilical humano (CTCUH) são fortes candidatas para uso nas lesões da medula espinhal devido à sua baixa imunogenicidade e pronta disponibilidade. O estudo avaliou os efeitos da administração de CTCUH na lesão isquêmica da medula espinhal em ratos. MÉTODOS: Quarenta ratos Wistar receberam injeção intratecal de 10 uL de solução de HemoHes (6 %) e albumina humana (20 %) contendo 1x104 CTCUH, 30 minutos antes (grupo Tcpré; n=10) e 30 minutos após (grupo Tcpós n=10) oclusão da aorta torácica descendente através de um balão intraluminal por 12 minutos. Os grupos controle receberam apenas a solução de Hemohes (6 %) e albumina humana (20 %) (grupo Cpré; n=10 e grupo Cpós; n=10). O período observacional, para avaliação da função motora dos animais, foi de 28 dias. Cortes de três segmentos tóraco-lombares da medula espinhal foram submetidos à análise histológica e imunohistoquímica para detecção de apoptose (TUNEL) e quantificação de células-tronco humanas hematopoiéticas CD45 +. RESULTADOS: Todos os grupos mostraram incidência semelhante de paraplegia e mortalidade. A média de pontuação da função motora não mostrou diferença durante o período observacional nos grupos, com exceção do grupo Tcpós o qual melhorou de 8,14 ± 8,6 para 14,28 ± 9,8 (p < 0,01). Número de neurônios viáveis foi maior no grupo Tcpós (p=0,14) e a média de apoptose foi mais baixa nesse mesmo grupo (p=0,048), porém sem diferença estatística significativa em relação ao controle. Foi confirmada a presença de células CD45 + quatro semanas após a injeção intratecal em ambos os grupos terapêuticos, principalmente, no grupo Tcpós. CONCLUSÕES: A injeção intratecal de CTCUH é factível e melhora a função motora da medula espinhal em um modelo de oclusão endovascular da aorta torácica descendente / BACKGROUND: Spinal cord ischemia remains a complication after surgical repair of descending and thoracoabdominal aortic diseases. OBJECTIVES: Stem cells have the potential to induce nervous tissue regeneration processes. Human stem cells derived from the umbilical cord are one of strong candidates used in cell therapy for spinal cord injury due to weak immunogenicity and ready availability. We sought to evaluate the use of Human Umbilical Cord Blood Stem Cells (HUCBSC) attenuates the neurologic effects of spinal cord ischemia. METHODS: Fourty Wistar rats received intrathecally injection of 10 uL Hemohes (6 %) and human albumin (20 %) solution contained 1x104HUCBSC, 30 minutes before (Tcpré group; n=10) and 30 minutes after (Tcpós group; n=10) descending thoracic aortic occlusion by intraluminal balloon during 12 minutes. Control groups received only PBS solution (Cpré group; n=10 and Cpós group; n=10). During a 28-day observational period, animals motor function was assessed. Three segments of thoraco-lombar spinal cord specimens were analyzed for histologic and immunohistochemical assessment for detection and quantification of human hematopoietic cells CD45+ and apoptosis (TUNEL). RESULTS: All groups showed similar incidence of paraplegia and mortality. The mean motor function scores showed no difference during time, excepting for Tpos group which improved from 8.14(8.6) to 14.28(9.8)(p < 0,01). Number of viable neurons was higher in Tcpós group (p = 0.14) and apoptosis average was lower in the same animals (p = 0.048), but showed no difference with its respective control. We confirmed the presence of CD45+ cells four weeks after intrathecal injection in both therapeutic groups but mainly in Tpos group. CONCLUSIONS: Intrathecal transplantation of HUCBSC is feasible and improved spinal cord function in a model of endovascular descending aortic occlusion

INTRODUÇÃO: Os enxertos vasculares sintéticos disponíveis atualmente apresentam baixos índices de patência, quando utilizados na revascularização de vasos de pequeno calibre, e possuem resultados inferiores quando comparados ao uso de veias autólogas em derivações infrageniculares. Nova prótese de pequeno calibre confeccionada em silicone (polidimetilsiloxano, PDMS) com reforço de tecido de poliéster foi desenvolvida e comparada à prótese de PTFE. OBJETIVOS: Analisar, em modelo experimental em coelhos, o tubo de PDMS como material para prótese vascular e compará-lo a prótese de PTFE. MÉTODOS: Quarenta coelhos foram submetidos a interposição na aorta infrarrenal de próteses de 4mm de diâmetro, sendo 20 animais com PDMS e 20 com PTFE (grupo controle). Foi medido o tempo de clampeamento e realizada arteriografia retrógrada da aorta para avaliar a patência das próteses. Para avaliar a endotelização das próteses foi realizada microscopia eletrônica de maneira amostral pareada. RESULTADOS: Vinte e cinco animais (62,5%) não apresentaram intercorrências pós-operatórias; oito (20%) morreram precocemente e sete (17,5%) ficaram paraplégicos no pós-operatório imediato (e foram sacrificados), sendo que esses animais não foram incluídos nas análises de patência. Não foi observada diferença entre os grupos quanto à evolução com complicações pós-operatórias (p=0,526) e quanto ao tempo de clampeamento da aorta (p=0,299). A patência em 30 dias foi de 100% para as duas próteses. Aos 60 dias, a taxa de patência do PDMS foi de 92,3% (± 7,4), e de 73,8% (±13,1) em 90 dias; as próteses de PTFE tiveram taxas de patência de 87,5% (± 11,7) aos 60 e 90 dias. Não foi observada diferença significativa entre as taxas de patência dos grupos (p=0,62). Não houve diferença siginificativa entre os grupos quanto ao grau de estenose das próteses patentes (p=0,650) à avaliação angiográfica. A microscopia eletrônica mostrou crescimento endotelial limitado às regiões próximas às anastomoses nos dois tipos de próteses. CONCLUSÃO: O PDMS mostrou-se passível de utilização como prótese vascular, com resultados comparáveis aos do PTFE no modelo utilizado / INTRODUCTION: Synthetic vascular grafts currently available have suboptimal patency rates in small-diameter vessels and inferior outcomes in below-the-knee arterial bypass procedures when compared to the use of autologous vein. A new small vessel prosthesis made of silicone (polydimethylsiloxane, PDMS) and reinforced with polyester fabric was developed and compared to the standard PTFE prosthesis. OBJECTIVES: On a rabbit experimental model, we compared the outcomes of new PDMS vascular prostheses with PTFE vascular prostheses. METHODS: Forty rabbits underwent infra-renal aorta replacement with 4 mm diameter prostheses, twenty animals with PDMS and twenty animals with PTFE (control group). Aortic clamping time was measured and retrograde aortic angiography was performed to assess patency. Histological graft samples were examined by electron microscopy to evaluate prostheses endothelialization. RESULTS: Twenty-five (62,5%) animals had good surgical outcome; eight animals (20%) expired and seven animals (17.5%) became paraplegic (and subsequently sacrificed) during early follow up and were not included in anastomosis patency analysis. Postoperative complications (death, paraplegia) rates (p=0,526) and aortic clamping times (p=0,299) were comparable in both groups. Patency rates in 30 days were 100% for both grafts. At 60 days, patency rate for PDMS was 92,3% (±7,4), and 73,8% (±13,1) at 90 days. PTFE grafts had patency rates of 87,5% (±11,7) at 60 and 90 days. No statistically significant difference was found in between groups for patency rates (p=0,62). No statistically significant difference for stenosis was found on angiographical analysis in between groups (p=0,650). Electron microscopy revealed limited anastomotic endothelial ingrowth in both prostheses used. CONCLUSION: In this experimental model, PDMS and PTFE vascular prostheses had comparable outcomes and PDMS prosthesis could be used as a vacular graft

Orientador: João Batista Campos Silva / Resumo: Nas últimas décadas, há uma crescente preocupação em mensurar os parâmetros dinâmicos do sangue, dadas as imensas perdas de vidas por doenças cardiovasculares sendo, muitas delas, por aneurismas. A formação e desenvolvimento de um aneurisma é, predominantemente, degenerativo e provém de uma complexa interação entre os efeitos biológicos da parede arterial, os estímulos de escoamento e tensões provenientes da hemodinâmica. A tensão cisalhante na parede e o cíclico campo de pressão são um dos principais fatores responsáveis pela formação e crescimento de um aneurisma. Logo, há a necessidade de se conhecer os campos de velocidades e pressão além das tensões cisalhantes e efetivas na parede. Uma análise numérica é mais promissora que uma experimental. Uma análise experimental in-vivo possui impasses éticos e morais, sem contar a necessidade de um grande investimento. Outra vantagem de um estudo numérico é a disponibilidade de softwares livres de extração de tomografias que permite a extração da geometria sem a necessidade de um método invasivo que ocorreria em estudo experimental in vivo. Portanto com o auxílio de simulações numéricas (Ansys®), considerando o efeito multi-física de interação fluido estrutura (FSI) pela metodologia de elementos e volumes finitos foi possível verificar o efeito dos fatores que levam a formação e crescimento de aneurisma na aorta abdominal. Os aneurismas estudados foram modelos geométricos e reais sendo um dos reais obtidos através de imagens DICOM... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: In recent decades, there is growing concern in measuring the dynamic parameters of the blood, given the immense loss of life from cardiovascular disease in human history, including, aneurysms. The formation and development of an aneurysm is predominantly degenerative and results from a complex interaction between the biological effects of the arterial wall and the flow and stress effects from hemodynamics. The stress in the wall and in the cyclic field of pressure is one of the main factors for the formation and growth of an aneurysm that degenerates until its rupture. Therefore, it is necessary to know the velocity and pressure fields as well as the shear stress and effective stress on the wall. A numerical analysis is more promising than an experimental one since an in-vivo experimental analysis has ethical and moral impasses, not counting the need for a large investment. Another advantage of a numerical study is the availability of free softwares for tomography analysis that allows the extraction of the geometry without the need for an invasive method that would occur in an in vivo experimental study. Therefore, with the aid of numerical simulations (Ansys®), considering the multi-physical effect of fluid structure interaction (FSI) by the methodology of finite elements and finite volumes it was possible to verify the effect of factors that lead to the formation and growth of abdominal aortic aneurysm. The studied aneurysms came from geometric models and from real examples... (Complete abstract click electronic access below) / Mestre

Materials which exhibit non-linear mechanical behaviors under large deformations are generally classified as “soft matter”. Elastomers represent an important class of soft materials which have wide commercial applications and isotropic non-linear behavior. In contrast, biological materials have anisotropic responses due to their heterogeneous and composite architectures. The underlying microstructure determines the arterial macroscopic behavior and is represented through constitutive models to describe the stress-strain relationships. Mechanical characterization and development of constitutive models that describe these non-linear and anisotropic properties are essential to our understanding of the structure-property relationships in these materials. In this study, we use two model systems to link the local microstructure to the overall macroscopic behaviors of soft matter. First, we delineate the roles of individual network topological factors in determining the overall macroscopic behavior of isotropic silicone elastomers using specimens fabricated with differential amounts of crosslinking. We performed mechanical experiments, within a theoretically motivated continuum mechanical framework, using a custom made planar biaxial testing instrument. These experiments demonstrate the contributions of physical entanglements and chemical crosslinks to the overall mechanical properties of silicone elastomers. Further, we show that the slip-link form of strain energy function is better suited to describe the material properties in the low to moderate regions of the stress-strain behavior. However, this model does not predict the stiffening response of elastomers at higher deformations, which is better captured using the Arruda-Boyce form of strain energy function. To explore the effects of individual topological factors on the overall network properties, we performed swelling experiments of silicone specimens in xylene and quantified variations in the polymer-solvent interaction parameter, χ, given by the Frenkel-Flory-Rehner (FFR) model. Further, we characterized the viscoelastic properties using dynamic mechanical analysis. Our results show that χ is not a constant, as assumed in the FFR model, but bears a linear relation to the equilibrium polymer volume fraction. To characterize the contribution of trapped entanglements to the overall mechanical behaviors, we use scaling laws in polymer physics and investigate the dependence of equilibrium volume fraction and experimentally obtained elastic moduli. Further, dynamic mechanical analysis demonstrated an increase in complex modulus with increase in the cross linking density. Finally, we examined variations in the uniaxial and the dynamical mechanical properties of silicone elastomers with storage time. Our results show that the time dependent increase in the modulus correlated with the formation of slip-links in the samples aged for a significantly long time in air. Together, these comprehensive studies show the importance of individual network features which affect the overall macroscopic properties of elastomers. Second, we use a multilayered and composite arterial model system to explore the passive material properties of arteries due to anisotropic layouts of extracellular matrix proteins, collagen and elastin. We characterized the mechanical properties of diseased human ascending thoracic aortic dissected (TAD) tissues, obtained from consenting patients undergoing emergency surgical repair to replace the diseased region, using multiple biaxial tests. We fit these results to micro structurally motivated Holzapfel-Gasser-Ogden model which is frequently used in the arterial mechanics literature. Our results show a higher stiffness for TAD tissues as compared to control aorta, without the presence of atherosclerotic plaques or other arterial disease. To study the directional variation in the mechanical properties of TAD tissues, we compared the stiffness in circumferential longitudinal directions at high and low stress region of equibiaxial experimental data. We observed no differences in the stiffness of TAD tissues in the circumferential and longitudinal directions. Further, we do not see any directional variations in the ultimate tensile stress, maximum extensibility, and modulus calculated in the low stretch region of uniaxial stress-strain response in TAD tissues. Histological analysis of TAD tissues showed a decrease in elastin content and an increase in collagen content as compared to control tissues. Higher TAD tissue stiffness also correlated with reduced elastin content in the arterial walls. To investigate the strain rate dependence of measured mechanical properties we use high testing rates of 1mm/sec to show that the TAD tissues have higher stiffness in the circumferential direction as compared to longitudinal direction. Finally, we used peel experiments to quantify the rupture potential of aortic dissected tissues. Our results show that TAD tissues have reduced delamination strength between layers as compared to control aortic tissues. To the best of our knowledge, no previous study has reported the mechanical property of human TAD tissues and these are the only biomechanical results on TAD tissues reported in specimens from South Asian patients. We hope that such studies will be useful for researchers who rely on microstructure based constitutive models to accurately describe the mechanical environment of cells which are important in the remodeling of tissues and in numerical models to assess mechanical criteria which may lead to the growth or dissection of arterial tissues.