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1.
ABCD (São Paulo, Impr.) ; 28(1): 28-31, 2015. graf
Article in English | LILACS | ID: lil-742748

ABSTRACT

BACKGROUND: The surgical treatment of advanced megaesophagus has no consensus, being esophagectomy the more commonly used method. Since it has high morbimortality - inconvenient for benign disease -, in recent years an alternative has been introduced: the esophageal mucosal resection. AIM: To compare early and late results of the two techniques evaluating the operative time, length of ICU stay; postoperative hospitalization; total hospitalization; intra- and postoperative complication rates; mortality; and long-term results. METHODS: Were evaluated retrospectively 40 charts, 23 esophagectomies and 17 mucosectomies. In assessing postoperative results, interviews were conducted by using a specific questionnaire. RESULTS: Comparing the means of esophagectomy and mucosal resection, respectively, the data were: 1) surgical time - 310.2 min and 279.7 min (p> 0.05); 2) length of stay in ICU - 5 days and 2.53 days (p <0.05); 3) total time of hospitalization - 24.25 days and 20.76 days (p> 0.05); 4) length of hospital stay after surgery - 19.05 days and 14.94 days (p> 0.05); 5) presence of intraoperative complications - 65% and 18% (p <0.05); 6) the presence of postoperative complications - 65% and 35% (p> 0.05). In the assessment of late postoperative score (range 0-10) esophagectomy (n = 5) obtained 8.8 points and 8.8 points also got mucosal resection (n = 5). CONCLUSIONS: Esophageal mucosal resection proved to be good alternative for surgical treatment of megaesophagus. It was advantageous in the immediate postoperative period by presenting a lower average time in operation, the total hospitalization, ICU staying and complications rate. In the late postoperative period, the result was excellent and good in both operations. .


RACIONAL: O tratamento cirúrgico do megaesôfago avançado não é consensual sendo mais comumente usada a esofagectomia. Por tratar-se de técnica que apresenta maior morbimortalidade e empregada em doença benigna, foi introduzida nos últimos anos, como alternativa, a mucosectomia esofágica. OBJETIVO: Comparar os resultados imediatos e tardios das duas técnicas avaliando-se os tempos operatório, de internação em UTI, de internação do pós-operatório, de internação total; taxas de complicações intra-operatórias e pós-operatórias; taxa de mortalidade; e resultados a longo prazo. MÉTODOS: Foram avaliados 40 prontuários, retrospectivamente, sendo 23 esofagectomias e 17 mucosectomias. Na avaliação dos resultados pós-operatórios, foram realizadas entrevistas, mediante uso de questionário específico. RESULTADOS: Comparando-se as médias da esofagectomia e mucosectomia, respectivamente, os dados foram: 1) tempo cirúrgico - 310,2 min e 279,7 min (p>0,05); 2) tempo de internação em UTI - 5 dias e 2,53 dias (p<0,05); 3) tempo de internação total - 24,25 dias e 20,76 dias (p>0,05); 4) tempo de internação após a operação - 19,05 dias e 14,94 dias (p>0,05); 5) presença de complicações intra-operatórias - 65% e 18% (p<0,05); 6) presença de complicações pós-operatórias imediatas - 65% e 35% (p>0,05). Na avaliação do escore pós-operatório tardio (escala 0-10) a esofagectomia (n=5) obteve 8,8 pontos e também 8,8 pontos obteve a mucosectomia (n=5). CONCLUSÕES: A mucosectomia esofágica mostrou-se boa alternativa no tratamento cirúrgico do megaesôfago avançado. Foi vantajosa no pós-operatório imediato por apresentar menor média de tempo na operação, na internação total, na UTI e no índice de complicações. No pós-operatório tardio, o resultado foi excelente e bom nas duas operações. .


Subject(s)
Animals , Male , Mice , Energy Metabolism , /metabolism , Insulin/metabolism , Myocardial Contraction/physiology , Myocytes, Cardiac/metabolism , Signal Transduction/physiology , Hypoxia/metabolism , Cells, Cultured , Clathrin/metabolism , /genetics , Mice, Transgenic , Myocytes, Cardiac/cytology , Protein Transport/physiology , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Sarcolemma/metabolism , Sarcolemma/ultrastructure
2.
Indian J Biochem Biophys ; 2013 Oct; 50(5): 428-435
Article in English | IMSEAR | ID: sea-150252

ABSTRACT

Membrane repair is a conserved cellular process, where intracellular vesicles translocate to sites of plasma membrane injury to actively reseal membrane disruptions. Such membrane disruptions commonly occur in the course of normal physiology, particularly in skeletal muscles due to repeated contraction producing small tears in the sarcolemmal membrane. Here, we investigated whether prolonged exercise could produce adaptive changes in expression levels of proteins associated with the membrane repair process, including mitsugumin 53/tripartite motif-containing protein 72 (MG53/TRIM72), dysferlin and caveolin-3 (cav3). Mice were exercised using a treadmill running protocol and protein levels were measured by immunoblotting. The specificity of the antibodies used was established by immunoblot testing of various tissue lysates from both mice and rats. We found that MG53/TRIM72 immunostaining on isolated mouse skeletal muscle fibers showed protein localization at sites of membrane disruption created by the isolation of these muscle fibers. However, no significant changes in the expression levels of the tested membrane repair proteins were observed following prolonged treadmill running for eight weeks (30 to 80 min/day). These findings suggest that any compensation occurring in the membrane repair process in skeletal muscle following prolonged exercise does not affect the expression levels of these three key membrane repair proteins.


Subject(s)
Animals , Carrier Proteins/metabolism , Caveolin 3/metabolism , Gene Expression Regulation , Male , Membrane Proteins/metabolism , Mice , Muscle, Skeletal/cytology , Muscle, Skeletal/physiology , Myocardium/cytology , Physical Conditioning, Animal , Protein Transport , Rats , Sarcolemma/metabolism , Time Factors
3.
Braz. j. med. biol. res ; 41(7): 615-620, July 2008. ilus, tab, graf
Article in English | LILACS | ID: lil-489520

ABSTRACT

Obesity is a complex multifactorial disorder that is often associated with cardiovascular diseases. Research on experimental models has suggested that cardiac dysfunction in obesity might be related to alterations in myocardial intracellular calcium (Ca2+) handling. However, information about the expression of Ca2+-related genes that lead to this abnormality is scarce. We evaluated the effects of obesity induced by a high-fat diet in the expression of Ca2+-related genes, focusing the L-type Ca2+ channel (Cacna1c), sarcolemmal Na+/Ca2+ exchanger (NCX), sarcoplasmic reticulum Ca2+ ATPase (SERCA2a), ryanodine receptor (RyR2), and phospholamban (PLB) mRNA in rat myocardium. Male 30-day-old Wistar rats were fed a standard (control) or high-fat diet (obese) for 15 weeks. Obesity was defined as increased percent of body fat in carcass. The mRNA expression of Ca2+-related genes in the left ventricle was measured by RT-PCR. Compared with control rats, the obese rats had increased percent of body fat, area under the curve for glucose, and leptin and insulin plasma concentrations. Obesity also caused an increase in the levels of SERCA2a, RyR2 and PLB mRNA (P < 0.05) but did not modify the mRNA levels of Cacna1c and NCX. These findings show that obesity induced by high-fat diet causes cardiac upregulation of Ca2+ transport_related genes in the sarcoplasmic reticulum.


Subject(s)
Animals , Male , Rats , Calcium Channels/genetics , Calcium-Binding Proteins/genetics , Calcium-Transporting ATPases/genetics , Myocardium/metabolism , Obesity/metabolism , Sarcoplasmic Reticulum Calcium-Transporting ATPases/genetics , Sodium-Calcium Exchanger/genetics , Calcium Channels/metabolism , Calcium-Binding Proteins/metabolism , Calcium-Transporting ATPases/metabolism , Homeostasis , Myocardium/chemistry , Obesity/genetics , Rats, Wistar , Reverse Transcriptase Polymerase Chain Reaction , RNA, Messenger , Sarcolemma/chemistry , Sarcolemma/metabolism , Sarcoplasmic Reticulum Calcium-Transporting ATPases/metabolism , Sodium-Calcium Exchanger/metabolism , Up-Regulation
4.
Indian J Physiol Pharmacol ; 2006 Apr-Jun; 50(2): 99-113
Article in English | IMSEAR | ID: sea-108723

ABSTRACT

This is a concise review of important calcium-transporters on the sarcolemma and organellar membranes of myocardial cells, and their functional roles in cell physiology. It briefly addresses L and T type calcium channels, store-operated calcium channel (SOC), sodium-calcium exchanger (NCX), and the plasma membrane calcium ATPase (PMCA) on the sarcolemma, ryanodine receptor (RyR), IP3 receptor (IP3R) and the sarcoplasmic reticulum (SR) calcium ATPase (SAERCA) on the SR membrane and their contributions to contraction and rhythm-generation. Several agonists and blockers for every transporter that are commonly used in research, and those with therapeutic applications have also been discussed.


Subject(s)
Animals , Calcium Channels/physiology , Calcium Channels, L-Type/physiology , Calcium Channels, T-Type/physiology , Calcium-Transporting ATPases/physiology , Cation Transport Proteins/physiology , Humans , Inositol 1,4,5-Trisphosphate Receptors , Myocardium/metabolism , Myocytes, Cardiac/metabolism , Plasma Membrane Calcium-Transporting ATPases , Receptors, Cytoplasmic and Nuclear/physiology , Ryanodine Receptor Calcium Release Channel/physiology , Sarcolemma/metabolism , Sarcoplasmic Reticulum Calcium-Transporting ATPases , Sodium-Calcium Exchanger/physiology
5.
Rev. chil. cardiol ; 25(1): 85-91, ene.-mar. 2006. ilus, tab
Article in Spanish | LILACS | ID: lil-485645

ABSTRACT

Antecedentes: Episodios breves de ejercicio previos a la oclusión prolongada de una arteria coronaria disminuyen el tamaño del infarto inducido por ésta. Objetivo: Dado que la administración intracoronaria de Ca2+ induce precondicionamiento, y el ejercicio probablemente aumenta el calcio citosólico, decidimos estudiar si el precondicionamiento por ejercicio está mediado por Ca2+. Material y método: Para ello analizamos el efecto del bloqueo de los canales de calcio del sarcolema, con verapamilo, sobre la acción precondicionante del ejercicio. Se midió tamaño del infarto en perros entrenados a correr en cinta sin finasignados aleatoriamente a los siguientes grupos. I: Isquemia inducida por oclusión coronaria durante 1 hora seguida de reperfusión por 4 hrs. E+I: Similar al grupo I, pero los perros hicieron ejercicio antes de inducir la isquemia. V+I: Similar al grupo I, pero se administró verapamilo antes de inducir la isquemia. V+E+I : Similar al grupo E+I, pero se administró verapamilo antes del ejercicio. Para estudiar el posible rol mediador del retículo sarcoplasmático (RS) en los efectos de la isquemia y de verapamilo, se midió la captación y la liberación de calcio en vesículas de RS de la pared del ventrículo izquierdo sometida a isquemia con o sin verapamilo en perros con y sin precondicionamiento con ejercicio. Los resultados, expresados como promedio +/- ES, se analizaron mediante ANOVA seguido del test de Holm para comparaciones múltiples. Resultados: Verapamilo revirtió el efecto protector del ejercicio sobre el tamaño del infarto (E+I: 6,0 +/- 9,4; N=12 vs V+E+I: 27,7+/-9,6; N=15; P<0.05), pero no modificó el efecto protector del ejercicio precondicionante sobre los trastornos de transporte de calcio en el RS inducidos por la isquemia. Conclusiones: Nuestros resultados sugieren que el precondicionamiento inducido por ejercicio está mediado por la entrada de calcio a la célula...


Background: Brief episodes of exercise prior to a prolonged occlusion of a coronary artery substantially reduce infarct size. Aim: Since the intracoronary administration of Ca2+ induces preconditioning and exercise most likely increases cytosolic calcium we put forward the hypothesis that preconditioning by exercise is mediated by calcium. Methods: For this purpose we analyzed the effect of verapamil, a sarcolemmal calcium channel blocker, on preconditioning by exercise. We measured infarct size in dogs randomly assigned to one of the following groups. I: Ischemia induced by coronary occlusion during 1 hour followed by reperfusion during 4 hours. E+I: Similar to group I, but the dogs run on a treadmill prior to ischemia. V+I: Similar to group I but verapamil was administered before the coronary occlusion. V+E+I: Similar to group E+I but verapamil was administered before exercise. SR vesicles from ventricular tissue were isolated from dogs subjected to the same experimental protocols and calcium release and active calcium uptake were measured. Results were expressed as Mean +/- SE and analyzed by ANOVA followed by Holm test for multiple comparisons. Results: Verapamil reverted the protective effect of exercise on infarct size (E+I: 6,0 +/- 9,4; N=12 vs V+E+I: 27,7 +/- 9,6;N=15; P<0.05) however it did not modify the protective effect of exercise on the alterations produced by ischemia on calcium transport in the RS. Conclusions: These results suggest that the preconditioning effect of exercise is mediated by calcium entering the cell through the sarcolemma but not by exercise effects on SR calcium transport.


Subject(s)
Animals , Calcium/metabolism , Myocardial Infarction/metabolism , Ischemia/metabolism , Ischemic Preconditioning, Myocardial , Verapamil/pharmacology , Analysis of Variance , Calcium Channel Blockers/pharmacology , Control Groups , Dogs , Myocardial Infarction/physiopathology , Exercise Test/methods , Sarcoplasmic Reticulum/metabolism , Sarcolemma , Sarcolemma/metabolism
7.
Medicina (B.Aires) ; 53(5): 445-58, sept.-oct. 1993. ilus
Article in Spanish | LILACS | ID: lil-129405

ABSTRACT

Es aceptado que los movimientos iónicos a través de diferentes sistemas membranosos (sarcolema, retículo, sarcoplásmico y mitocondria) juegan un papel importante en el metabolismo del músculo cardíaco. Por otra parte, tanto su participación relativa como el gasto de energía asociado a dichos movimientos, no han sido definitivamente establecidos. Mediciones biofísicas y bioquímicas de los diferentes mecanismos de intercambio iónico, han provisto datos que llevaron a postular diferentes modelos funcionales para el metabolismo de reposo y el metabolismo activo del músculo cardíaco. El presente trabalho analisa, desde un punto de vista energético, datos bioquímicos y biofísicos extraídos de la literatura calculando el rango del consumo de energia que sería atribuible a cada mecanismo. Particularmente, son analizados los movimientos de sodio, potasio y calcio durante el estado de reposo y/o el estado activo y se discute la participación fraccional de las distintas organelas (sarcolema, retículo sarcoplásmico y mitocondria). Con este análisis y a partir de la cantidad conocida de energía liberada ( o la cantidad de oxígeno consumido) por el músculo es posible determinar la existencia de suficiente energía para un modelo dado de intercambio iónico durante el proceso de excitación-contracción. Además del análisis mencionado, se presenta una revisión de estudios energéticos realizados en condiciones patológicas. En particular, se analizan patologías con compromiso energético directo tal como la hipertrofia cardíaca, la isquemia y la anoxia en las que la alteración de los mecanismo de transporte iónico parecen jugar un papel crucial


Subject(s)
Humans , Calcium/metabolism , Myocardial Contraction/physiology , Energy Metabolism , Potassium/metabolism , Sodium/metabolism , Heart Diseases/physiopathology , Mitochondria, Heart/metabolism , Sarcoplasmic Reticulum/metabolism , Sarcolemma/metabolism
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