Diss. (sammanfattning) Linköping : Univ., 2004. / I publikationen felaktig serie: Linköping studies in health sciences. Härtill 4 uppsatser.

A isquemia aguda mesentérica é uma condição de grande emergência vascular, que é fatal na população mundial em 60% a 80% dos casos. O objetivo desse trabalho foi estudar, os efeitos da isquemia/reperfusão intestinal sobre o receptor P2X2 e diferentes classes neuronais no plexo mioentérico. Foram analisados o íleo de ratos: controle, Sham e isquemia/reperfusão intestinal (I/R-i) com de 24h e 1 semana de reperfusão. Foram realizadas colocalização do receptor P2X2 com a NOS, ChAT, Calb, Calr, S100 e anti-HuC/D. Os resultados mostraram diminuição de neurônios P2X2-ir colocalizados com a NOS, ChAT e Hu, e um aumento com S100 no grupo I/R-i 1 semana. A densidade apresentou um aumento de células P2X2-ir e S100 e diminuição de ChAT e Hu no grupo I/R-i de 1 semana. O perfil neuronal apresentou um aumento nos neurônios NOS-ir, ChAT, Calb (Dogiel Tipo II) e Calr. Conclui-se que a isquemia levou a alterações diferenciadas no receptor P2X2, células gliais e neurônios entéricos, que podem causar disfunções gastrintestinais, como por exemplo, problemas na motilidade intestinal. / The acute mesenteric ischemia is a vascular condition of extreme emergency, which is fatal in the world population by 60% to 80% of cases. The aim of this work was to study the effects of intestinal ischemia/reperfusion on the P2X2 receptor and different neuronal classes in the myenteric plexus. We analyzed the ileum of rats: control, Sham and ischemia/reperfusion (I/R-i) with 24 hours and 1 week of reperfusion. The colocalization were performed by P2X2 receptor with NOS, ChAT, Calb, Calr, S100 and anti-HUC/D. The results showed a decrease of P2X2-ir neurons colocalizated with ChAT and Hu, and an increase in the group with S100 in the I/R-i 1 week group. The density of cells showed an increase of P2X2-ir and S100 and a decrease of Hu and ChAT in I/R-i 1 week group. The profile area showed an increase in NOS-ir, ChAT-ir, Calb (Dogiel Type II) and Calr-ir neurons. We conclude that ischemia led to different changes in P2X2 receptor, enteric neurons and glial cells, which can cause gastrointestinal disorders, such as intestinal motility disorder.

Admite-se que mais de 40% das crianças são acometidas pela desnutrição crônica em Moçambique (África Oriental). A doença pode estar relacionada, entre outros fatores, à qualidade da dieta que é oferecida à população, já que é bastante precária, pois exibe sérias deficiências de ferro, gordura e, principalmente, proteína animal em sua composição. Essa insuficiência proteica poderia acarretar em prejuízo ao desenvolvimento do organismo, pois a proteína animal é considerada uma boa fonte de aminoácidos essenciais, em decorrência de sua maior digestibilidade e absorção no intestino delgado, quando comparadas às fontes de origem vegetal. Na presente pesquisa foi reproduzida em laboratório, a dieta básica da população de Moçambique (DM), com o objetivo de avaliar seus efeitos nos componentes do plexo mioentérico e na mucosa dos segmentos do intestino delgado de ratos Wistar. Para isso, os animais foram divididos nos grupos Controle, com dieta AIN-93G com adição de 20% de caseína (NN21 e NN42); Dieta de Moçambique (DM21 e DM42) e Dieta Moçambique suplementada, acrescida de 20% de caseína (NM21 e NM42); e grupo Renutrido (RM42), composto por animais do grupo DM21 que, a partir do 22º dia, receberam a dieta NM até atingirem 42 dias de vida. Os segmentos foram coletados e submetidos às técnicas histoquímicas da NADH-diaforase e da NADPH-diaforase para evidenciação de neurônios do plexo mioentérico; histológicas (HE, Picro-sírius, Weigert) para avaliação da parede intestinal, mucosa, gânglios e seu tecido conjuntivo associado; de microscopia eletrônica de varredura (MEV) para observação da estrutura da mucosa; e de microscopia eletrônica de transmissão (MET) para a ultraestrutura dos componentes ganglionares. Estatisticamente, o peso corporal e o comprimento dos animais submetidos à dieta de Moçambique estavam abaixo dos valores encontrados para os animais controle. Na análise qualitativa, observou-se a presença de fibras elásticas, elaunínicas e oxitalânicas, assim como predominância de fibras colágenas do tipo I nos grupos NN42 e DM42, e do tipo III nos grupos NM42 e RM42 ao redor dos gânglios. A mucosa apresentou uma menor área no grupo DM21 com recuperação em DM42, com diminuição da altura das vilosidades nos dois grupos. Foram observadas alterações na organização do retículo endoplasmático rugoso e disposição dos materiais fibrilares e granulares do nucléolo dos animais DM. Sob MEV as vilosidades do grupo DM42 apresentaram superfície mais lisa, com poucas delimitações entre elas. A densidade dos neurônios reativos à NADH diminuiu de 21 para 42 dias em todos os grupos; porém, o DM21 e DM42 apresentou uma maior densidade. Os neurônios reativos à NADPH apresentaram a diminuição da densidade de 21 para 42 dias nos grupos DM e NM, quando comparados ao controle. Assim, conclui-se que a dieta vegetal de Moçambique levou à alterações na morfologia da mucosa, parede intestinal e neurônios entéricos, como uma forma de adaptação à dieta imposta / It is assumed that more than 40% of children are affected by chronic malnutrition in Mozambique (East Africa). The disease may be related, among other factors, the quality of diet that is offered to the population, since it is quite precarious, because it displays serious deficiencies of iron, fat and especially animal protein in their composition. This protein failure could result in damage to the development of the organism, as animal protein is considered a good source of essential amino acids, due to its higher digestibility and absorption in the small intestine when compared to vegetable sources. In this research has been reproduced in the laboratory, the staple diet of the population of Mozambique (DM), in order to evaluate its effects on components of the myenteric plexus and the mucosa of the small intestine segments of Wistar rats. For this, the animals were divided into control groups with AIN-93G diet with the addition of 20% casein (NN21 and NN42); Diet Mozambique (DM21 and DM42) and diet supplemented Mozambique, plus 20% casein (NM21 and NM42); and Refeeding group (RM42), consisting of the animals DM21 group, from the 22th day, given NM diet until they reached 42 days of life. The segments were collected and submitted to histochemical techniques of NADH-diaphorase and NADPH-diaphorase for disclosure of neurons of the myenteric plexus; histologic (HE, Sirius red, Weigert) for evaluation of the intestinal wall, mucosa, lymph nodes and its associated connective tissue; scanning electron microscopy (SEM) for observation of mucosal structure; and Transmission electron microscopy (TEM) ultrastructure to ganglion components. Statistically, body weight and length of the animals submitted to Mozambique diet were below the values found for control animals. Qualitative analysis showed the presence of elastic fibers, and elauninic oxytalan, and predominance of type I collagen fibers in the NN42 and DM42 groups, and type III in the NM42 and RM42 groups around the ganglia. The mucosa showed a smaller area in DM21 group recovery DM42, with a decrease in villus height in both groups. There have been changes in the organization of the rough endoplasmic reticulum and arrangement of fibrillar and granular materials nucleolus of DM animals. Under SEM the villi of the DM42 group showed smoother surface, with few boundaries between them. The density of reactive NADH decreased from 21 to 42 days in all groups; however, the DM21 and DM42 had a higher density. Reactive neurons to NADPH had decreased from 21 to 42 days density in DM and NM groups when compared to the control. Thus, it is concluded that vegetable diet Mozambique led to changes in the morphology of the mucosa, the intestinal wall and enteric neurons, as a way to adapt to the imposed diet

nÃo hà / Està bem estabelecido que a regulaÃÃo dos lÃquidos corporais seja garantida pela interaÃÃo funcional entre os sistemas cardiovascular e renal. Atualmente, evidÃncias clÃnicas e experimentais sugerem que o trato gastrintestinal (TGI) ajusta seu padrÃo motor e absortivo apÃs variaÃÃes agudas da volemia. Embora a insuficiÃncia renal parcial ou total promova variaÃÃes dos volumes corporais circulantes, poucos estudos apontam a relaÃÃo entre a insuficiÃncia renal e o funcionamento do trato gastrintestinal. Neste trabalho, estudamos o efeito da dieta salina sobre a motilidade gastrintestinal [esvaziamento gÃstrico (EG) e o trÃnsito gastrintestinal (GI) de lÃquidos] e transporte intestinal (IT) de Ãgua e eletrÃlitos (Na+, K+ e Cl-) em ratos nefrectomizados parcialmente (nefre5/6) ou falso-operados (FO) em condiÃÃes de hidrataÃÃo e desidrataÃÃo. Para tanto, 138 ratos Wistar, machos (180-220g), submetidos à nefrectomia parcial (nefre5/6) em duas etapas (0 e 7 dias). ApÃs nefre 5/6 ou FO, os animais foram distribuÃdos em dois grupos diferentes, a saber: raÃÃo e salina 1% ou raÃÃo e Ãgua. ApÃs 3d e, sob jejum de 24h com livre acesso à salina ou Ãgua, 1,5ml da refeiÃÃo teste (vermelho fenol 0,5mg/ml e glicose 5%) foi administrada por gavagem em animais acordados. Decorridos 10, 20 ou 30min, os animais foram sacrificados por deslocamento cervical, seguidos da exÃrese das vÃsceras abdominais para determinaÃÃo da taxa de EG e trÃnsito GI. AlÃm disso, um experimento semelhante foi realizado utilizando 5ml de polietilenoglicol-PEG (30% - 20.000 DA) injetado por via subcutÃnea em ratos quatro horas antes do inÃcio do experimento, a fim de simular as condiÃÃes de desidrataÃÃo. Para os estudos do transito intestinal de Ãgua e eletrÃlitos, os animais anestesiados, foram submetidos à perfusÃo ileal com Ringer + vermelho fenol durante 60min. Para todos os experimentos, monitoramos os parÃmetros hemodinÃmicos (pressÃo arterial-PA, pressÃo venosa central-PVC, frequÃncia cardÃaca-FC e volume sanguÃneo-VS) e ainda as concentraÃÃes bioquÃmicas plasmÃticas de Ur, Cr, Na+, K+ e Cl- foram determinadas. Em relaÃÃo ao grupo FO a dieta salina nÃo modificou o EG ou transito GI, nem os parÃmetros hemodinÃmicos ou bioquÃmicos, porÃm promoveu secreÃÃo ileal de Ãgua e eletrÃlitos. Por outro lado, a dieta salina nos animais nefre5/6 promoveu: i) aumento da retenÃÃo gÃstrica de 47%, 26% e 38% (10, 20 e 30 minutos de tempo pÃs-prandial, respectivamente), ii aceleraÃÃo do trÃnsito GI, iii) aumento na secreÃÃo ileal de Ãgua e eletrÃlitos e, iv) aumento da PA, PVC, FC, BV. A desidrataÃÃo aguda com PEG preveniu as alteraÃÃes da motilidade, da secreÃÃo GI e dos parÃmetros hemodinÃmicos secundÃrios hipervolemia crÃnica à custa da nefrectomia 5/6 associada à dieta salina. A motilidade gastrintestinal e o ajuste da absorÃÃo, devido à dieta salina sobre os animais submetidos à nefrectomia parcial, estÃo relacionados aos nÃveis do volume do sangue e pode ser revertida por desidrataÃÃo aguda. Em conclusÃo, trato gastrointestinal pode ajustar tanto o seu motor, bem como atividades de absorÃÃo apÃs desequilÃbrios crÃnicos volume de sangue. / It is well established that the regulation of the corporal fluids is guaranteed by functional interaction between cardiovascular and renal systems. Currently, clinical and experimental evidences suggest that gastrointestinal (GI) tract (GIT) adjust their motor and absorptive activities due to acute changes in the blood volume. Although total or partial renal failure promotes corporal fluids changing. Several studies indicate a relationship among renal failure and GIT functions. In this work, we study the effect of a salt diet on GIT motility [gastric emptying (GE) and GI transit of liquids] and intestinal transport (IT) of H2O and electrolytes (Na+, K+ and Cl-) in partial nephrectomized (nefre5/6) or false-operated (FO) rats under hydrated and dehydrate conditions. For that, 138 male Wistar rats (180-220g) submitted to partial nephrectomy (nefre5/6) in two steps (0 and 7 days). After nefre5/6 or FO procedures, animals were distributed into 2 different experiments both containig two groups as follows: feed+1% saline or feed+water. For the hydrate conditions experiment, after 3d and under 24-hour fasting with free access to water or saline, 1.5ml of the test meal (phenol red 0.5 mg/mL containg 5% glucose) was gavaged in the awake animals. Next 10, 20 or 30 minutes, the animals were sacrificed by cervical dislocation. Following, excision of the abdominal viscera was performed in order to determine the GE rate and GI transit. Additionally, similar experiment were performed using 5mL of polyethylene glycol-PEG (30% - 20,000 DA) injected subcutaneous in the rats 4 hours before the beginning of the experiment in order to simulate the dehydrate conditions. For IT studies, anesthetized animals underwent ileal perfusion with Ringer+phenol red solution and were monitored along 60 min. For all experiments, mean arterial pressure - MAP, central venous pressure-CVP, heart rate-HR and blood volume-BV were monitored. Also, plasmatic concentrations of Ur, Cr, Na+, K+ and Cl- were determined. Compared with FO group, nefre5/6 did not change the GE or GI transit, neither hemodynamic or biochemical parameters, but promotes ileal secretion of water and electrolytes. On the other hand, comparing the salt diet and standard diet, the nefre5/6 animals caused: i) increases on the gastric retention of 47%, 26% and 38% (at 10, 20 and 30 minutes of postprandial time, respectively), ii) acceleration of the GI transit, iii) increases on the ileal secretion of water and electrolytes and, iv) increases BP, CVP, HR and BV. However, changes on the other plasmatic biochemical parameters were not observed in this study. The acute dehydration with PEG prevented gut motility and hemodynamic changes and the increase of gastrointestinal secretions. Gastrointestinal motility and absorptive adjustments due to salt diet on the partial nephrectomized animals, is related to blood volume levels and, can be reversed by acute dehydration. In conclusion, gastrointestinal tract can adjust both their motor as well as absorptive activities after chronic blood volume imbalances.

Thesis (Ph. D.)--University of Oklahoma. / Includes bibliographical references (leaves 148-162).

Inadequate delivery of nutrition to the critically ill is common, and may adversely affect clinical outcomes, including survival. This thesis reports studies designed to characterise the gastrointestinal dysfunction underlying feed intolerance in the critically ill, as well as the pathophysiology of these dysfunctions, and investigate potential therapeutic measures. While it has been established that enteral nutrition is frequently unsuccessful in the critically ill, assessment of the success of feeding in an Australian intensive care unit (ICU) had not been performed previously. A prospective survey examined the incidence of, and risk factors for, feed intolerance in the ICU at the Royal Adelaide Hospital and demonstrated that, in 40 patients receiving enteral feeding, only about 60% of their nutritional requirements were met at the end of the first week. The main cause for this lack of success was large gastric residual volumes, indicative of delayed gastric emptying (GE). This study, accordingly, quantified the limitations of nutritional delivery in contemporary practice in a local ICU. The results suggest that a better understanding of the pathogenesis underlying this problem is warranted in order to direct research into improved therapies. Scintigraphy is the most accurate technique to measure GE, but is difficult to perform in the ICU. A simpler, more convenient, test would increase the accessibility of GE measurement for both research and clinical purposes. A study comparing a breath test technique and gastric residual volume measurement to the scintigraphic measurement of GE in 25 mechanically ventilated patients demonstrated that GE measured by a breath test technique closely correlated with that measured by scintigraphy. While the breath test had a specificity of 100% it only had a sensitivity of about 60% in the prediction of delayed GE. Similarly, gastric residual volume measurement correlated with scintigraphic measurement of GE but also lacked sensitivity. The breath test has previously been demonstrated to be highly reproducible and it represents a useful option for repeated measurement of GE in the same patient. It is therefore likely to be useful to determine changes in GE over time or in response to a therapeutic intervention. There is a lack of information about the prevalence and determinants of delayed GE in the critically ill. Previous studies have substantial limitations and scintigraphic measurement of GE has only rarely been used. A study comparing GE measured by scintigraphy in 25 patients to 14 healthy subjects demonstrated that GE was delayed in approximately 50% of the ICU patients (>10% retention at 4h) and markedly delayed in about 20% (>50% retention at 4h). Patients with trauma and sepsis appeared to have a relatively higher prevalence of delayed GE (80% and 75% respectively). In addition, the longer the patient had been in ICU the more normal the rate of GE. Quantification of delayed GE may prove useful by defining patients who may benefit from preventative or therapeutic options. The abnormalities in gastrointestinal motility underlying delayed GE in the critically ill are poorly characterised. Simultaneous manometric and gastric emptying measurements were performed in 15 mechanically ventilated patients and 10 healthy subjects. These studies demonstrated that delayed GE was associated with reduced antral activity, increased pyloric activity and increased retrograde duodenal activity in the patients. Persistent fasting motility during feeding was also frequently observed. Furthermore, the feedback response to small intestinal nutrients was enhanced. This latter observation may provide an explanation for the delayed GE and warrants further investigation. Recent studies suggest that the hormone cholecystokinin may be a mediator of increased small intestinal feedback and, if confirmed, this has clear therapeutic implications. Nutrient absorption has rarely been measured in the critically ill. GE and glucose absorption (using 3-O-methyl glucose) were measured simultaneously in 19 ICU patients and compared to 19 healthy subjects. Glucose absorption was shown to be markedly reduced in the patients. Slow GE was associated with delayed, and reduced, absorption. However, glucose absorption was also reduced in patients with normal GE suggesting that reduced glucose absorption in critical illness is only partly due to delayed GE. Accordingly, measures to improve the effectiveness of GE and thereby improve overall nutritional status may be compromised by abnormal small intestinal absorption. The mechanisms underlying this warrant further investigation. A number of therapeutic options directed at improving the delivery of nutrition were examined. In a study involving 20 mechanically ventilated patients, administration of 200mg erythromycin intravenously was shown to be superior to placebo for treating feed intolerance. The optimal dose of erythromycin, however, was unclear. In a subsequent study involving 35 ICU patients, GE was measured using a breath test technique, before and after 2 different doses of erythromycin or placebo and a ‘low’ intravenous dose (70mg) of erythromycin appeared to be as effective as a ‘moderate’ dose (200mg). Both doses were only effective in subjects who had delayed GE at baseline. Based on the outcome of these studies, low doses of erythromycin have subsequently been routinely used to treat feed intolerance in the critically ill patients at the Royal Adelaide Hospital. Animal and human studies suggested that the antibiotic, cefazolin, may have a prokinetic effect. Cefazolin, however, did not demonstrate similar prokinetic activity at a ‘low’ dose (50mg) in a critically ill cohort. The results of this study do not support the use of this agent, at this dose, as a prokinetic, in this population. If nasogastric administration of nutrition proves unsuccessful an alternative is to infuse nutrient directly into the small intestine. However, the placement of feeding tubes distal to the pylorus is technically difficult. A novel technique for postpyloric tube insertion was examined with promising results. In summary, the studies described in this thesis have provided a number of insights relevant to the management of the critically ill by quantifying the prevalence of feed intolerance and delayed GE, characterising some of the disturbances in gastrointestinal motility underlying this problem, and evaluating a number of therapeutic interventions. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1345143 / Thesis (Ph.D.) -- University of Adelaide, School of Medicine, 2008

Inadequate delivery of nutrition to the critically ill is common, and may adversely affect clinical outcomes, including survival. This thesis reports studies designed to characterise the gastrointestinal dysfunction underlying feed intolerance in the critically ill, as well as the pathophysiology of these dysfunctions, and investigate potential therapeutic measures. While it has been established that enteral nutrition is frequently unsuccessful in the critically ill, assessment of the success of feeding in an Australian intensive care unit (ICU) had not been performed previously. A prospective survey examined the incidence of, and risk factors for, feed intolerance in the ICU at the Royal Adelaide Hospital and demonstrated that, in 40 patients receiving enteral feeding, only about 60% of their nutritional requirements were met at the end of the first week. The main cause for this lack of success was large gastric residual volumes, indicative of delayed gastric emptying (GE). This study, accordingly, quantified the limitations of nutritional delivery in contemporary practice in a local ICU. The results suggest that a better understanding of the pathogenesis underlying this problem is warranted in order to direct research into improved therapies. Scintigraphy is the most accurate technique to measure GE, but is difficult to perform in the ICU. A simpler, more convenient, test would increase the accessibility of GE measurement for both research and clinical purposes. A study comparing a breath test technique and gastric residual volume measurement to the scintigraphic measurement of GE in 25 mechanically ventilated patients demonstrated that GE measured by a breath test technique closely correlated with that measured by scintigraphy. While the breath test had a specificity of 100% it only had a sensitivity of about 60% in the prediction of delayed GE. Similarly, gastric residual volume measurement correlated with scintigraphic measurement of GE but also lacked sensitivity. The breath test has previously been demonstrated to be highly reproducible and it represents a useful option for repeated measurement of GE in the same patient. It is therefore likely to be useful to determine changes in GE over time or in response to a therapeutic intervention. There is a lack of information about the prevalence and determinants of delayed GE in the critically ill. Previous studies have substantial limitations and scintigraphic measurement of GE has only rarely been used. A study comparing GE measured by scintigraphy in 25 patients to 14 healthy subjects demonstrated that GE was delayed in approximately 50% of the ICU patients (>10% retention at 4h) and markedly delayed in about 20% (>50% retention at 4h). Patients with trauma and sepsis appeared to have a relatively higher prevalence of delayed GE (80% and 75% respectively). In addition, the longer the patient had been in ICU the more normal the rate of GE. Quantification of delayed GE may prove useful by defining patients who may benefit from preventative or therapeutic options. The abnormalities in gastrointestinal motility underlying delayed GE in the critically ill are poorly characterised. Simultaneous manometric and gastric emptying measurements were performed in 15 mechanically ventilated patients and 10 healthy subjects. These studies demonstrated that delayed GE was associated with reduced antral activity, increased pyloric activity and increased retrograde duodenal activity in the patients. Persistent fasting motility during feeding was also frequently observed. Furthermore, the feedback response to small intestinal nutrients was enhanced. This latter observation may provide an explanation for the delayed GE and warrants further investigation. Recent studies suggest that the hormone cholecystokinin may be a mediator of increased small intestinal feedback and, if confirmed, this has clear therapeutic implications. Nutrient absorption has rarely been measured in the critically ill. GE and glucose absorption (using 3-O-methyl glucose) were measured simultaneously in 19 ICU patients and compared to 19 healthy subjects. Glucose absorption was shown to be markedly reduced in the patients. Slow GE was associated with delayed, and reduced, absorption. However, glucose absorption was also reduced in patients with normal GE suggesting that reduced glucose absorption in critical illness is only partly due to delayed GE. Accordingly, measures to improve the effectiveness of GE and thereby improve overall nutritional status may be compromised by abnormal small intestinal absorption. The mechanisms underlying this warrant further investigation. A number of therapeutic options directed at improving the delivery of nutrition were examined. In a study involving 20 mechanically ventilated patients, administration of 200mg erythromycin intravenously was shown to be superior to placebo for treating feed intolerance. The optimal dose of erythromycin, however, was unclear. In a subsequent study involving 35 ICU patients, GE was measured using a breath test technique, before and after 2 different doses of erythromycin or placebo and a ‘low’ intravenous dose (70mg) of erythromycin appeared to be as effective as a ‘moderate’ dose (200mg). Both doses were only effective in subjects who had delayed GE at baseline. Based on the outcome of these studies, low doses of erythromycin have subsequently been routinely used to treat feed intolerance in the critically ill patients at the Royal Adelaide Hospital. Animal and human studies suggested that the antibiotic, cefazolin, may have a prokinetic effect. Cefazolin, however, did not demonstrate similar prokinetic activity at a ‘low’ dose (50mg) in a critically ill cohort. The results of this study do not support the use of this agent, at this dose, as a prokinetic, in this population. If nasogastric administration of nutrition proves unsuccessful an alternative is to infuse nutrient directly into the small intestine. However, the placement of feeding tubes distal to the pylorus is technically difficult. A novel technique for postpyloric tube insertion was examined with promising results. In summary, the studies described in this thesis have provided a number of insights relevant to the management of the critically ill by quantifying the prevalence of feed intolerance and delayed GE, characterising some of the disturbances in gastrointestinal motility underlying this problem, and evaluating a number of therapeutic interventions. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1345143 / Thesis (Ph.D.) -- University of Adelaide, School of Medicine, 2008

Orientador: Madileine Francely Américo / Resumo: Os imunossupressores são utilizados após o transplante de órgãos e no tratamento de doenças autoimunes, desencadeando diversos efeitos colaterais. No esquema tríplice de imunossupressão pós-transplante, cada droga ou a combinação delas podem alterar a estrutura e/ou funcionamento do trato gastrintestinal. Apesar da importância do trato gastrintestinal e de conhecer os efeitos da ingesta oral de imunossupressores, há poucos estudos enfocando esses aspectos e vários desafios éticos para essas avaliações no homem. Desse modo, objetivou-se avaliar as alterações provocadas pela imunossupressão nos parâmetros de esvaziamento gástrico, frequência e amplitude das contrações gástricas, bem como as alterações histológicas no estômago de ratos. Para isso foram utilizados a Biosusceptometria de Corrente Alternada (BAC) e a Eletrogastrografia (EGG). No primeiro capítulo, avaliou-se individualmente sete imunossupressores de diferentes classes (Tacrolimo, Ciclosporina, Micofenolato Mofetil, Azatioprina, Sirolimo, Everolimo e Prednisona) comumente utilizados na terapia imunossupressora. Todos os imunossupressores estudados, exceto o Micofenolato Mofetil causaram alguma alteração nos parâmetros gastrintestinais analisados em ratos. Já o segundo capítulo apresenta os efeitos da terapia imunossupressora combinada, baseada em três classes de imunossupressores (inibidores da calcineurina, antimetabólitos e glicocorticoides). Um dos grupos experimentais recebeu Tacrolimo associado à Micofenolato S... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Immunosuppressants are used after organ transplantation and in the treatment of autoimmune diseases, triggering several side effects. In the triple regimen of post - transplant immunosuppression, each drug or combination of them may alter the structure and / or function of the gastroin testinal tract. Despite the importance of gastrointestinal tract and knowledge of the effects of oral intake of immunosuppressants, there are few studies focusing on these aspects and several ethical challenges for these evaluations in humans. The aim of t his study was to evaluate the effects provoked by immunosuppression in gastric emptying parameters, frequency and amplitude of gastric contractions, as well as the histological aspects in the stomach of rats. Alternating Current Biosusceptometry (BAC) and Electrogastrography (EGG) were used. In the first chapter, seven immunosuppressants from different classes (Tacrolimus, Cyclosporine, Mycophenolate Mofetil, Azathioprine, Sirolimus, Everolimus and Prednisone) commonly used in immunosuppressive therapy were evaluated individually. All immunosuppressants studied except Mycophenolate Mofetil , caused some alteration in the gastrointestinal parameters analyzed in rats. The second chapter presents the effects of combined immunosuppressive therapy based on three c lasses of immunosuppressants (calcineurin inhibitors, antimetabolites and glucocorticoids). One of the experimental groups received Tacrolimus associated with Mycophenolate Sodium and Pr... (Complete abstract click electronic access below) / Doutor

Made available in DSpace on 2015-07-22T20:49:55Z (GMT). No. of bitstreams: 0 Previous issue date: 2010-05-26 / Objetivo: Determinar o efeito do ácido ursodesoxicólico e o papel da mucosa no aparecimento de alterações motoras, na musculatura esofagiana de cobaias. Métodos: Trabalho experimental realizado com 18 cobaias albinas do sexo masculino pesando entre 200 e 250g. Os animais foram distribuídos em 03 grupos, sendo assim constituídos: Grupo (A)- 06 animais formaram o grupo experimental – Esôfago com mucosa, Grupo (B)- 06 animais formaram o grupo experimental – Esôfago sem mucosa e Grupo (C)- 06 animais formaram o grupo controle. Os animais foram sacrificados e o esôfago distal foi removido. Após identificação da transição epitelial escamo-colunar, foi realizada a secção ao nível da mesma desprezando-se a câmara gástrica. Os espécimes de esôfago foram encaminhados para prova de avaliação contrátil, utilizando-se câmaras de perfusão de órgãos e um sistema de aquisição de dados com o programa KITCAD 8. Os espécimes foram mantidos em solução salina oxigenada por 01 hora, com estiramento de 01 grama a fim de readquirirem sua tensão basal e foram estimulados com 40mM de KCl. Após a verificação da manutenção contrátil e avaliação da amplitude contrátil inicial, os fragmentos foram banhados na solução de 100 mM de ácido ursodesoxicólico, nos grupos A e B, e em solução salina fisiológica, no grupo C, por 01 hora, e, então, novamente estimulados com 40mM de KCl, e realizados cinco estímulos com intervalo de cinco minutos para o registro da amplitude contrátil. Resultados: A média da amplitude de contração antes da incubação (pré) variou entre os grupos (p=0,006) com médias de 1,319(A), 0,306(B) e 1,795(C). Após a incubação (pós), a média da amplitude de contração foi de 0,709 , 0,278 e 1,353 para os grupos A, B e C, respectivamente. Antes da incubação, não houve diferença na amplitude de contração entre os grupos A e C (p=0,633) e houve diferença entre os grupos A e B (p=0,039) e B e C (p=0,048). Após a incubação, quando comparamos as diferenças das médias dentro dos grupos nos momentos pré e pós, encontramos apenas diferenças no grupo A (p=0,030). Conclusões: A exposição esofagiana ao ácido ursodexosicólico, componente da bile, induz a uma diminuição da amplitude de contração esofagiana. A mucosa esofagiana desempenha importante papel na motilidade esofagiana. / Background and Aims: Esophageal motor abnormalities are frequently found in patients with gastroesophageal reflux disease. The role of bile in reflux-induced dysmotility is still elusive. Furthermore, it is questionable weather mucosal or muscular stimulation leads to motor modification. The aims of this study were: (a) analyze the effect of bile infusion in the amplitude of esophageal contractions and (b) analyze the effect of mucosal vs muscular stimulation. Methods: 18 guinea-pig esophagi were isolated and its contractility assessed with force transducers. Three groups were studied. In group A (n= 6) the entire esophagus was used and incubated in 100 ìML ursodeocycholic acid for 2 hours. In group B (n=6) the mucosal layer was removed and the muscular layer incubated in 100 ìML ursodeocycholic acid for 1 hours. In group C (n=6) (control group) the entire esophagus was used and incubated in saline solution. In all groups, five sequential contractions spaced by 1 minute were measured before and after incubation. Contractions were recorded after KCl 40 mM stimulation. Results: Contractions before incubation did differed among groups (p= 0,006) and averaged 1,319(A),0,306(B) and 1,795(C). After incubation amplitude of contraction was 0,709 , 0,278 and 1,353 for groups A, B and C respectively. Before incubation there were no diferrences between groups A and C (p=0,633) there was difference between groups A and B (p=0,039) and B and C (p=0,048). After incubation when we compare average within groups (before and after) there was difference only in group A (p=0,030). Conclusion: Our results show that bile exposure may induce ineffective esophageal motility and the mucosa seems to take an important role in esophageal motility. Disclosure Statement: No author has commercial associations that might create a conflict of interest. No competing financial interests exist. / TEDE / BV UNIFESP: Teses e dissertações

CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior / Estudamos o efeito do citrato de sildenafil (ViagraÂ), vasodilatador largamente utilizado na terapÃutica da disfunÃÃo erÃtil, sobre o comportamento motor do trato gastrintestinal (TGI) de ratos Wistar. Para tanto, utilizamos 175 animais machos, pesando entre 200 a 350g, distribuÃdos nos quatro seguintes grupos de estudo: efeitos do citrato de sildenafil sobre o i) esvaziamento gÃstrico (EG) e os trÃnsitos gastrintestinal (GI) e ii) intestinal de lÃquido em ratos acordados; iii) a complacÃncia gÃstrica de ratos anestesiados e iv) a contratilidade de tiras isoladas do duodeno de ratos ex vivo. i) Avaliamos, em 64 ratos acordados sob jejum e livre acesso à Ãgua por 24h, o efeito da injeÃÃo (0,2mL; e.v.) de sildenafil (4mg/Kg) ou veÃculo (HCl 0,01N) sobre o EG e o trÃnsito GI de lÃquido, bem como sobre a pressÃo arterial (PA). Mediante gavagem, 1,5mL da refeiÃÃo-teste (vermelho de fenol - 0,5mg/mL em glicose a 5%) foi injetada no estÃmago. Depois de 10, 20 ou 30min, sacrificamos os animais e, apÃs laparotomia, obstruÃmos o piloro, o cÃrdia e o Ãleo terminal. Removemos e dividimos o TGI em: estÃmago e segmentos consecutivos do intestino delgado (40% iniciais; 30% mediais e 30% terminais). ApÃs o processamento destas porÃÃes viscerais, determinamos as absorbÃncias das amostras a 560nm. A retenÃÃo fracional de vermelho fenol em cada segmento permitiu o cÃlculo do EG e trÃnsito GI. Em um grupo separado de animais, a PA foi monitorada continuamente por meio de um sistema digital de aquisiÃÃo de dados durante 20min antes e 30min apÃs o tratamento com sildenafil ou diluente. Comparado ao grupo controle, houve aumento significativo da retenÃÃo gÃstrica (44,2Â2,0 vs 53,2Â2,1; 25,4Â1,3 vs 37,3Â1,6; 20,9Â2,5 vs 32,5Â2,9%) nos animais tratados com sildenafil e sacrificados aos 10, 20, ou 30min, respectivamente, bem como retarde significativo no trÃnsito GI. Embora o sildenafil tenha provocado hipotensÃo, a PA retoma nÃveis basais logo apÃs 10min. O prÃ-tratamento com omeprazol (bloqueador da secreÃÃo Ãcida estomacal) nÃo modificou o efeito do sildenafil sobre os valores de retenÃÃo gÃstrica e intestinal nem nos nÃveis de PA. ii) Noutros animais (n=44), sob jejum de 24h e dotados previamente (3d) de uma cÃnula crÃnica no bulbo duodenal, estudamos o efeito do sildenafil sobre a progressÃo ao longo do intestino delgado de uma refeiÃÃo teste (10MBq de TecnÃcio ligado a fitato e diluÃdo em 1mL de salina 0,9%). Decorridos 20, 30 ou 40min da injeÃÃo (0,2mL e.v.) de sildenafil (4mg/Kg) ou diluente (HCL 0,01N), sacrificamos os animais e, apÃs laparotomia e remoÃÃo do TGI, dividimo-o em: estÃmago, cinco segmentos congruentes e consecutivos de intestino delgado e o intestino grosso. A contagem da radiatividade foi determinada num colimador de gama-cÃmara. O sildenafil promoveu retarde (p<0,05) do TI, indicado pelos retardes dos centros geomÃtricos da refeiÃÃo de 2,8&#61617; 0,2 vs 3,3&#61617; 0,1; 3,0&#61617; 0,2 vs 3,7&#61617; 0,1 e 3,4&#61617; 0,1 vs 4,2&#61617; 0,2 em relaÃÃo ao grupo controle, aos 20, 30 ou 40min. iii) Os estudos de complacÃncia gÃstrica foram conduzidos em 39 ratos anestesiados, sob jejum de 24h. As variaÃÃes do volume gÃstrico (VG), foram medidas por pletismografia, enquanto a PA foi monitorada continuamente por um sistema digital de aquisiÃÃo de dados. Em relaÃÃo aos valores basais (2,91Â0,19mL) o sildenafil (3mg/Kg â e.v.) aumentou (p<0,05) o VG apÃs 10, 20 e 30min (3,08Â0,18; 3,10Â0,17 e 3,09Â0,17mL). A PA basal (105,8Â2,28mmHg) caiu significativamente com o sildenafil (59,8Â3,2; 64,8Â3,7 e 59,3Â4,6mmHg) enquanto o diluente (HCl 0,01N) nÃo modificou seja o VG ou a PA. O prÃ-tratamento mediante esplancnotomia ou injeÃÃo e.v. com azul de metileno (3mg/Kg-bloqueador da guanilato ciclase), L-NNA (3mg/Kg-bloqueador da NO sintetase) ou propranolol (2mg/Kg-Ã-bloqueador) preveniram o aumento do VG pelo sildenafil; jà o pÃs-tratamento com nitroprussiato de sÃdio (1mg/Kg - e.v.) o ampliou significativamente. iv) Avaliamos ainda o efeito do sildenafil sobre a contratilidade de tiras isoladas do duodeno de ratos ex vivo (n=28), sacrificados por deslocamento cervical. Tiras dissecadas do duodeno foram suspensas longitudinalmente em cuba de vidro (10mL), plena de soluÃÃo de Tyrode (37oC e pH 7,4), e submetidas a uma tensÃo inicial de 1g. ApÃs 1h de estabilizaÃÃo, a contratilidade espontÃnea ou induzida das tiras foi registrada continuamente por um sistema digital de aquisiÃÃo de dados. O sildenafil em doses crescentes e cumulativas (0,1 a 300Âmol/L) relaxou (EC50 de 9,6Âmol/L) o duodeno, mais atà que o zaprinaste ou a papaverina (bloqueadores de FDEs) (EC50 91,6 e 78,5Âmol/L, nesta ordem). Observamos ademais que o sildenafil inibiu as contraÃÃes induzidas por acetilcolina ou carbacol (IC50 26,7 e 16,2Âmol/L, respectivamente). Jà o prÃ-tratamento com azul de metileno, ODQ (bloqueador da guanilato ciclase) ou L-NAME (bloquedor da NO sintetase), mas nÃo o D-NAME (isÃmero inativo da NO sintetase) preveniram o efeito do sildenafil. O efeito mio-relaxante do sildenafil foi ampliado pela L-arginina (substrato do NO sintetase) ou nitroprussiato de sÃdio (doador de NO). O prÃ-tratamento com forskolina (estimulador da adenilato ciclase) tambÃm aumentou o efeito mio-relaxante do sildenafil. Em resumo, observamos que o sildenafil diminui a motilidade gastrintestinal, retardando o EG, os trÃnsitos GI e intestinal de lÃquido em ratos acordados; aumenta a complacÃncia gÃstrica em ratos anestesiados alÃm de apresentar efeitos antiespasmÃdico e mio-relaxante sobre tiras isoladas de duodeno de ratos ex vivo; por estimulaÃÃo do sistema nervoso simpÃtico e tendo como provÃvel mecanismo de aÃÃo ao nÃvel do miÃcito gastrintestinal a via do NO/GMP cÃclico. / We evaluated the effect of sildenafil citrate (ViagraÂ) a vasodilator largely used for the treatment of male erectile dysfunction, on the gastrointestinal motility in rats. Experiments were performed on 175 male, Wistar rats, weighing 200-350g. Four groups of study were done: the sildenafil effects on the: i) Gastric emptying (GE) and gastrointestinal (GI) transit and ii) Intestinal transit (IT) of liquid in awake rats; iii) Gastric compliance in anesthetized rats and iv) Contractility of rat duodenal isolated strips. i) In 64 rats fasted for 24h with previous vascular access (right jugular vein and left carotid artery), we studied the effect of an i.v. injection (0.2mL) of sildenafil (4mg/Kg) or vehicle (0.01N HCl) on GE and GI transit of a liquid meal, as well as on arterial pressure (AP) in a separated group of rats. Animals were gavage-fed with 1.5mL of a test meal (0.5mg/mL of phenol red in 5% glucose). After 10, 20 or 30min, animals were sacrificed and submitted to a laparotomy to obstruct the pylorus, cardia and terminal ileus. The gut was removed and then divided into: stomach and consecutive three small intestine segments (40% proximal; 30% medial and 30% terminal). After processing these segments, the dye retention was determined at 560nm. The percentage of dye retention in each segment permitted to evaluate GE and GI transit. Arterial pressure was continuously monitored by a digital acquisition system during 20min before and 30min after sildenafil injection. We observed a significant increase of gastric retention in sildenafil treated rats at 10, 20, or 30min after the test meal (44,2Â2,0 vs 53,2Â2,1; 25,4Â1,3 vs 37,3Â1,6; 20,9Â2,5 vs 32,5Â2,9%, respectively), as well as a significant GI transit delay. Despite of sildenafil inducing hypotension, AP returned to basal levels 10min afterwards. Acid gastic secretion blocking pre-treatment with omeprazol did not modify the sildenafil effect on gastric retention, GI transit or AP. ii) In another group we evaluated the sildenafil (4mg/Kg) or diluente (0.01N HCl, 0.2mL) effects on the IT in awake rats, fasted for 24h. Animals were studied 3d after the insertion of a silastic cannula (0.6cm ID) into the duodenal bulb. We evaluated the progression of a radioactive liquid test meal fed (10MBq of 99mTc â 1mL of saline 0,9%) administered through the inserted cannula into the small intestine. After 20, 30 or 40min, animals were sacrificed by anesthetic overdose. After laparotomy, we removed and divided the gut in: stomach, five congruent and consecutive segments of the small intestine and the large intestine. Radioactivity counting was obtained in a gamma-chamber collimator. Sildenafil promoted an IT delay (p<0.05), indicated by shifting the center of mass to the proximal portions of the TGI (2.8Â0.2 vs 3.3Â0.1; 3.0Â0.2 vs 3.7Â0.1 and 3.4Â0.1 vs 4.2Â0.2) in relation to control group. iii) Gastric compliance study was performed on 39 anesthetized rats after 24h of fasting. Gastric volume (GV) variations were measured by plethysmography while AP was continuously monitored. We have also observed that GV increased (p<0.05) after sildenafil treatment (3mg/Kg - e.v) (3.08Â0.18; 3.10Â0.17 and 3.09Â0.17mL vs 2.91Â0.19mL) at 10, 20 and 30min after drug administation, respectively. Basal AP (105.8Â2.28mmHg) dropped by the sildenafil injection (59.8Â3.2; 64.8Â3.7 and 59.3Â4.6mmHg-p<0.05) while vehicule (0.01N HCl) did not change either GV or AP. After splanchnotomy or pre-treatments (e.v.) with methylene blue (3mg/Kg-guanilate cyclase blocker), L-NNA (3mg/Kg - NO synthase blocker) or propranolol (2mg/Kg - Ã-blocker) prevented GV increase due to sildenafil; while post-treatment with sodium nitroprusside (1mg/Kg - NO donor) raised it. iv) The in vitro contractility studies were performed on isolated duodenal strips obtained from rats (n=28) killed by cervical dislocation. Duodenal strips were suspended longitudinally in a glass chamber (10mL), filled with Tyrode solution (37oC and pH 7.4). After 1h of stabilization under 1g of initial tension, the spontaneous or induced contractility were continuously recorded by a digital acquisition system. Increasing and cummulative doses of sildenafil (0.1 to 300Âmol/L) relaxed (9.6Âmol/L of EC50) the duodenal strips. This effect was more intense than those displayed by zaprinast or papaverine (PDEs blockers) (91.6 and 78.5Âmol/L of EC50, in this order). Sildenafil showed significant antispasmodic and myorelaxant effects on the duodenal contractions induced by acetylcholine or carbamylcholine (IC50 26.7 and 16.2Âmol/L, respectively). Pre-treatment with methylene blue, ODQ (guanilato cyclase blocker) or L-NAME (NO synthase blocker) also prevented these sildenafil effects, but D-NAME (an inactive substrate for NO synthase) did not. Myorelaxant sildenafil effect was reverted by L-arginine (substrate for NO synthase) and contrarily it was largely increased by sodium nitroprusside. Forskolin adenylate cyclase activation pre-treatment also increased the myorelaxant effect of sildenafil. In summary, we have observed that sildenafil slowed down the gastrointestinal motility, delaying GE, GI and intestinal transits of a liquid meal in awake rats; Gastric compliance was also increased in anesthetized rats treated with sildenafil. Sildenafil also exhibited both antispasmodic and myorelaxant effects on isolated strips of duodenum of ex vivo rats. Besides central or peripheral sympathetic nervous system activation, sildenafil possibly acts at the gastrointestinal myocite level by activating the NO/GMPc system.