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1.
Clin J Gastroenterol ; 10(4): 361-363, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28589502

RESUMO

A 45-year-old woman visited our hospital complaining of abdominal pain 1 week after undergoing an annual medical checkup. Her vital signs and blood test results were normal, but tenderness was found in the lower abdomen. A high-density round structure found at the midline of the lower abdomen on an abdominal radiograph was thought to be an accumulation of barium (a barolith) from upper gastrointestinal barium radiography. Two liters of an oral gastrointestinal cleaning agent was administered, but defecation did not occur. Lower gastrointestinal endoscopy revealed that the barolith was impacted at the sigmoid colon. We unsuccessfully attempted to move it using a pressurized water jet and forceps, but it was too large to be captured by the net. Therefore, we broke it down using a snare. After a successful endoscopic procedure, 120 mL of a glycerin enema solution was injected through the forceps opening, causing the barolith to be excreted. There is only one similar case of successful endoscopic treatment of a barolith in the literature.


Assuntos
Sulfato de Bário/efeitos adversos , Meios de Contraste/efeitos adversos , Obstrução Intestinal/cirurgia , Litíase/cirurgia , Doenças do Colo Sigmoide/cirurgia , Colo Sigmoide/cirurgia , Colonoscopia , Feminino , Humanos , Obstrução Intestinal/etiologia , Litíase/induzido quimicamente , Pessoa de Meia-Idade , Doenças do Colo Sigmoide/etiologia
2.
World J Gastroenterol ; 22(21): 4988-98, 2016 Jun 07.
Artigo em Inglês | MEDLINE | ID: mdl-27275091

RESUMO

AIM: To provoke persistent/chronic multiorgan inflammatory response and to contribute to stones formation followed by fibrosis in hepatobiliary and pancreatic tissues. METHODS: Tumor necrosis factor receptors 1 and 2 (TNFR1/R2) deficient mice reared in-house were given dibutyltin dichloride (DBTC) twice within 10 d by oral gavage delivery. Sham control animals received vehicle treatment and naïve animals remained untreated throughout the study. Animals were monitored daily for symptoms of pain and discomfort. The abdominal and hindpaw hypersensitivity were assessed with von Frey microfilaments. Exploratory behaviors were recorded at the baseline, after initiation of treatment, and before study termination. Histopathological changes were examined postmortem in tissues. Collagen accumulation and fibrosis were confirmed with Sirius Red staining. RESULTS: Animals lost weight after oral administration of DBTC and developed persistent inflammatory abdominal and hindpaw hypersensitivity compared to sham-treated controls (P < 0.0001). These pain related secondary mechanical hypersensitivity responses increased more than 2-fold in DBTC-treated animals. The drastically diminished rearing and grooming rates persisted after DBTC administration throughout the study. Gross as well as micropathology at one month confirmed that animals treated with DBTC developed chronic hepatobiliary injuries evidenced with activation of stellate cells, multifocal necrosis, fatty degeneration of hepatocytes, periportal infiltration of inflammatory cells, and prominent biliary ductal dilation. The severity of hepatitis was scored 3.7 ± 0.2 (severe) in DBTC-treated animals vs score 0 (normal) in sham-treated animals. Fibrotic thickening was extensive around portal ducts, in hepatic parenchyma as well as in lobular pancreatic structures and confirmed with Sirius Red histopathology. In addition, pancreatic microarchitecture was presented with distortion of islets, and parenchyma, infiltration of inflammatory cells, degeneration, vacuolization, and necrosis of acinar cells and distention of pancreatic ducts. Extent of pancreatic damage and pancreatitis were scored 3.6 ± 0.4 (severe) for DBTC-treated in contrast to score 0 (normal) in sham-treated animals. The gall bladder became expanded with ductal distention, and occasional bile stones were detected along with microscopic hepatic lesions. DBTC-treated animals developed splenic hypertrophy with increased weight and length (P < 0.01) along with thymic atrophy (P < 0.001). Finally, colitic lesions and colitis were prominent in DBTC-treated animals and scored 3.4 ± 0.3 (moderately severe) vs 0 (normal) for the sham-treated animals. CONCLUSION: This is the first report of chronic inflammatory multiorgan hepatobiliary pancreatitis, along with fibrosis and calculi formation induced reliably utilizing oral DBTC administration in TNFR1/R2 deficient mice.


Assuntos
Ductos Biliares/metabolismo , Doença Hepática Induzida por Substâncias e Drogas/metabolismo , Colangite/metabolismo , Litíase/metabolismo , Cirrose Hepática Experimental/metabolismo , Fígado/metabolismo , Pâncreas/metabolismo , Pancreatite/metabolismo , Receptores Tipo II do Fator de Necrose Tumoral/deficiência , Receptores Tipo I de Fatores de Necrose Tumoral/deficiência , Dor Abdominal/induzido quimicamente , Dor Abdominal/genética , Dor Abdominal/metabolismo , Animais , Comportamento Animal , Ductos Biliares/patologia , Doença Hepática Induzida por Substâncias e Drogas/etiologia , Doença Hepática Induzida por Substâncias e Drogas/genética , Doença Hepática Induzida por Substâncias e Drogas/psicologia , Colangite/induzido quimicamente , Colangite/genética , Colangite/psicologia , Colite/induzido quimicamente , Colite/genética , Colite/metabolismo , Comportamento Exploratório , Predisposição Genética para Doença , Asseio Animal , Células Estreladas do Fígado/metabolismo , Células Estreladas do Fígado/patologia , Hiperalgesia/induzido quimicamente , Hiperalgesia/genética , Hiperalgesia/metabolismo , Litíase/induzido quimicamente , Litíase/genética , Litíase/psicologia , Fígado/patologia , Cirrose Hepática Experimental/induzido quimicamente , Cirrose Hepática Experimental/genética , Cirrose Hepática Experimental/psicologia , Camundongos Knockout , Compostos Orgânicos de Estanho , Percepção da Dor , Pâncreas/patologia , Células Estreladas do Pâncreas/metabolismo , Células Estreladas do Pâncreas/patologia , Pancreatite/genética , Pancreatite/psicologia , Fenótipo , Receptores Tipo I de Fatores de Necrose Tumoral/genética , Receptores Tipo II do Fator de Necrose Tumoral/genética , Baço/metabolismo , Baço/patologia , Redução de Peso
3.
Oxid Med Cell Longev ; 2015: 813737, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25883748

RESUMO

Nephrolithiasis is a complex disease that results from a combination of factors related to both urine composition and kidney morphoanatomy. Development of calcium oxalate monohydrate papillary calculi is linked to initial subepithelial calcification of renal papilla. Progressive tissue calcification depends on preexisting injury and involves reactive oxygen species. Many plant extracts that protect against oxidative stress manifest antilithiasic activity. Our study focused on determining the effects of polyphenols on a lithiasis rat model. Rats were pretreated with polyphenols and grape seed extracts, followed by posterior induction of hyperoxalosis via treatment with ethylene glycol plus NH4Cl. The concentrations of calcium and other elements in kidney were determined, along with histological examination of kidney and 24 h urine analysis. Significant differences were observed in the renal calcium content between the control plus ethylene glycol-treated group and the epicatechin plus ethylene glycol-treated, red grape seed extract plus ethylene glycol-treated, and white grape seed extract plus ethylene glycol-treated groups, with reductions of about 50%. The antioxidant activity of polyphenols extracted from red and white grape seeds may be critical in the prevention of calcium oxalate monohydrate papillary calculus formation, particularly if calculi are induced by lesions caused by cytotoxic compounds with oxidative capacity.


Assuntos
Nefropatias/patologia , Rim/efeitos dos fármacos , Polifenóis/farmacologia , Vitis/química , Cloreto de Amônio/toxicidade , Animais , Peso Corporal/efeitos dos fármacos , Cálcio/análise , Cálcio/urina , Catequina/farmacologia , Etilenoglicol/toxicidade , Extrato de Sementes de Uva/química , Rim/metabolismo , Rim/patologia , Nefropatias/induzido quimicamente , Nefropatias/prevenção & controle , Litíase/induzido quimicamente , Litíase/patologia , Litíase/prevenção & controle , Magnésio/análise , Magnésio/urina , Masculino , Fósforo/análise , Fósforo/urina , Polifenóis/isolamento & purificação , Polifenóis/uso terapêutico , Ratos , Ratos Wistar , Sementes/química , Sementes/metabolismo , Vitis/metabolismo
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