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1.
Rev. chil. urol ; 79(1): 51-53, 2014. ilus
Article in Spanish | LILACS | ID: lil-783419

ABSTRACT

La extravasación espontánea de orina, descrita por Albarrán y publicada por Sole se consideraba como un hallazgo radiológico poco frecuente y la definió en 198 como la salida de orina fuera del tracto urinario en ausencia de trauma, de intervención quirúrgica previa o reciente y tampoco sin antecedente de instrumentación urológica o de urografía excretora practicada con compresión externa. Se presenta a un paciente de 28 años, sin antecedentes de interés, que acudió con cuadro astenia de 1 mes de evolución, asociado a dolor en fosa lumbar izquierda. Que fue estudiado mediante ecografía y tomografía computarizada (TC). Las exploraciones radiológicas identificaron múltiples litiasis en uréter proximal y distal izquierdo. Voluminosa colección de baja densidad rodeando al riñón izquierdo, limitada por la fascia pararrenal sugestiva de urinoma, identificando solución de continuidad en cáliz superior, que se comunica con el urinoma. El tratamiento inicial del paciente fue la colocación de Nefrostomía percutánea de urgencia, para realizar posteriormente, ureteroscopia con ascensión de las litiasis y extracción de estas mediante pielolitotomía abierta. Conclusión: El conocimiento de la clínica y de los hallazgos radiológicos de la extravasación urinaria espontánea por litiasis ureteral en las distintas pruebas de imágenes son cruciales para el manejo de los pacientes afectados por esta infrecuente complicación...


Spontaneous extravasation of urine, described by Albarran and published by Sole was considered a rare radiological finding in 198 and defined as the flow of urine out of the urinary tract in the absence of trauma, previous surgery or recent nor no history of urological instrumentation or excretory urography performed with external compression. We report a patient of 28 years, with no history of interest came with asthenia of 1 month’s duration, associated with pain in left lumbar fossa. That was studied by ultrasound and computed tomography (CT). The radiological identified multiple stones in proximal and distal left ureter. Collection bulky low density surrounding the left kidney limited by suggesting pararenal urinoma fascia, identifying continuity solution upper calyx, which communicates with the urinoma. The patient’s initial treatment was percutaneous nephrostomy placement of urgency for later ascension of the stones with ureteroscopy and removal of these by open pyelolithotomy. The knowledge of the clinical and radiological findings of spontaneous urinary extravasation with ureteral stones in various imaging tests are crucial for the management of patients affected by this rare complication...


Subject(s)
Humans , Male , Adult , Kidney Diseases/etiology , Urine , Urologic Surgical Procedures/methods , Ureterolithiasis/surgery , Ureterolithiasis/complications , Urinoma
2.
Phytomedicine ; 16(10): 904-15, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19524419

ABSTRACT

Budlein A has been reported to exert some analgesic and anti-inflammatory properties. In this study, we have evaluated its effect on LPS-induced leukocyte recruitment in vivo and the mechanisms involved in its anti-inflammatory activity. In vivo, intravital videomicroscopy was used to determine the effects of budlein A on LPS-induced leukocyte-endothelial cell interactions in the murine cremasteric microcirculation. In vitro, the effects of budlein A on LPS-induced cytokine, chemokine and nitrites release, T-cell proliferative response as well as cell adhesion molecule expression (CAM) were evaluated. In vivo, intraperitoneal administration of budlein A (2.6 mM/kg) caused a significant reduction of LPS-induced leukocyte rolling flux, adhesion and emigration by 84, 92 and 96% respectively. In vitro, T-cell proliferative response was also affected by budlein A. When murine J774 macrophages were incubated with the sesquiterpene lactone, LPS-induced IL-1beta, tumor necrosis factor-alpha (TNF-alpha) and keratinocyte-derived chemokine (KC) release were concentration-dependently inhibited. In human umbilical vein endothelial cells (HUVECs), budlein A also reduced the production of TNF-alpha, monocyte chemoattractant protein-1 (MCP-1), IL-8, nitrites and CAM expression elicited by LPS. Budlein A is a potent inhibitor of LPS-induced leukocyte accumulation in vivo. This effect appears to be mediated through inhibition of cytokine and chemokine release and down-regulation of CAM expression. Thus, it has potential therapeutic interest for the control of leukocyte recruitment that occurs in different inflammatory disorders.


Subject(s)
Asteraceae/chemistry , Endothelial Cells/drug effects , Immunosuppressive Agents/isolation & purification , Lactones/pharmacology , Leukocyte Rolling/drug effects , Sesquiterpenes/pharmacology , Animals , Cell Adhesion Molecules/metabolism , Cell Communication/drug effects , Cell Line , Cell Proliferation/drug effects , Chemokines/metabolism , Dexamethasone , Humans , Lactones/isolation & purification , Lipopolysaccharides , Macrophages/drug effects , Male , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Microcirculation , Nitric Oxide/metabolism , Nitrites/metabolism , Plant Extracts/pharmacology , Sesquiterpenes/isolation & purification , T-Lymphocytes/drug effects
3.
Eur J Pharm Biopharm ; 70(3): 784-90, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18640269

ABSTRACT

PGE(2), an arachidonic acid metabolite produced by various type of cells regulates a broad range of physiological activities in the endocrine, cardiovascular, gastrointestinal, and immune systems, and is involved in maintaining the local homeostasis. In the immune system, PGE(2) is mainly produced by APCs and it can suppress the Th1-mediated immune responses. The aim of this study was to develop PGE(2)-loaded biodegradable MS that prolong and sustain the in vivo release of this mediator. An o/w emulsion solvent extraction-evaporation method was chosen to prepare the MS. We determined their diameters, evaluated the in vitro release of PGE(2), using enzyme immunoassay and MS uptake by peritoneal macrophages. To assess the preservation of biological activities of this mediator, we determined the effect of PGE(2) released from MS on LPS-induced TNF-alpha release by murine peritoneal macrophages. We also analyzed the effect of encapsulated PGE(2) on inflammatory mediators release from HUVECs. Finally, we studied the effect of PGE(2) released from biodegradable MS in sepsis animal model. The use of this formulation can provide an alternative strategy for treating infections, by modulating or inhibiting inflammatory responses, especially when they constitute an exacerbated profile.


Subject(s)
Dinoprostone/pharmacology , Endothelial Cells/drug effects , Immunologic Factors/pharmacology , Inflammation Mediators/metabolism , Macrophages, Peritoneal/drug effects , Microspheres , Phagocytosis/drug effects , Animals , Cells, Cultured , Chemistry, Pharmaceutical , Chemokine CCL2/metabolism , Delayed-Action Preparations , Dinoprostone/chemistry , Disease Models, Animal , Drug Compounding , Emulsions , Endothelial Cells/immunology , Humans , Immunologic Factors/chemistry , Macrophages, Peritoneal/immunology , Mice , Nitric Oxide/metabolism , Oils/chemistry , Particle Size , Sepsis/immunology , Sepsis/prevention & control , Solubility , Time Factors , Tumor Necrosis Factor-alpha/metabolism , Water/chemistry
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