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1.
Hepatobiliary Pancreat Dis Int ; 15(6): 647-654, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27919855

RESUMO

BACKGROUND: Uncoupling protein 2 (UCP2) has been suggested to inhibit mitochondrial production of reactive oxygen species (ROS) by decreasing the mitochondrial membrane potential. Experimental acute pancreatitis is associated with increased UCP2 expression, whereas UCP2 deficiency retards regeneration of aged mice from acute pancreatitis. Here, we have addressed biological and molecular functions of UCP2 in pancreatic stellate cells (PSCs), which are involved in pancreatic wound repair and fibrogenesis. METHODS: PSCs were isolated from 12 months old (aged) UCP2-/- mice and animals of the wild-type (WT) strain C57BL/6. Proliferation and cell death were assessed by employing trypan blue staining and a 5-bromo-2'-deoxyuridine incorporation assay. Intracellular fat droplets were visualized by oil red O staining. Levels of mRNA were determined by RT-PCR, while protein expression was analyzed by immunoblotting and immunofluorescence analysis. Intracellular ROS levels were measured with 2', 7'-dichlorofluorescin diacetate. Expression of senescence-associated beta-galactosidase (SA beta-Gal) was used as a surrogate marker of cellular senescence. RESULTS: PSCs derived from UCP2-/- mice proliferated at a lower rate than cells from WT mice. In agreement with this observation, the UCP2 inhibitor genipin displayed dose-dependent inhibitory effects on WT PSC growth. Interestingly, ROS levels in PSCs did not differ between the two strains, and PSCs derived from UCP2-/- mice did not senesce faster than those from corresponding WT cells. PSCs from UCP2-/- mice and WT animals were also indistinguishable with respect to the activation-dependent loss of intracellular fat droplets, expression of the activation marker alpha-smooth muscle actin, type I collagen and the autocrine/paracrine mediators interleukin-6 and transforming growth factor-beta1. CONCLUSIONS: A reduced proliferative capacity of PSC from aged UCP2-/- mice may contribute to the retarded regeneration after acute pancreatitis. Apart from their slower growth, PSC of UCP2-/- mice displayed no functional abnormalities. The antifibrotic potential of UCP2 inhibitors deserves further attention.


Assuntos
Proliferação de Células , Células Estreladas do Pâncreas/metabolismo , Proteína Desacopladora 2/metabolismo , Animais , Biomarcadores/metabolismo , Proliferação de Células/efeitos dos fármacos , Células Cultivadas , Relação Dose-Resposta a Droga , Perfilação da Expressão Gênica , Regulação da Expressão Gênica , Genótipo , Iridoides/farmacologia , Camundongos Endogâmicos C57BL , Camundongos Knockout , Células Estreladas do Pâncreas/efeitos dos fármacos , Células Estreladas do Pâncreas/patologia , Fenótipo , Espécies Reativas de Oxigênio/metabolismo , Transdução de Sinais , Proteína Desacopladora 2/antagonistas & inibidores , Proteína Desacopladora 2/deficiência , Proteína Desacopladora 2/genética
2.
J Surg Case Rep ; 2023(5): rjad232, 2023 May.
Artigo em Inglês | MEDLINE | ID: mdl-37153831

RESUMO

Common left iliac vein compression, otherwise known as May-Thurner Syndrome (MTS), is a medical condition that refers to chronic compression of an anatomical variant of the left iliac vein by the overlying right common iliac artery and is a predisposing factor for deep vein thrombosis of the left lower limb (LDVT). Although MTS is not often, its true prevalence is underestimated due to misdiagnose, fact that can result to life-threatening conditions such as the development of LDVT and pulmonary embolism. In this paper, we present a case of MTS presenting at our department with unilateral leg swelling without LDTV that was treated through endovascular management along with long-term anticoagulation. With this presentation, the authors wish to emphasise the importance of MTS as a frequently under-diagnosed condition that needs to be ruled out in unilateral left leg swelling with or without LDVT.

3.
J Surg Case Rep ; 2023(5): rjad250, 2023 May.
Artigo em Inglês | MEDLINE | ID: mdl-37201107

RESUMO

Spontaneous idiopathic pneumoperitoneum (SIP) is a rare condition in the surgical practice. We introduce a case of an alcoholic male who presented with nausea, vomiting and diarrhea without clinical signs of peritonitis. A computed tomography of the abdomen showed free air distributed mainly along the ascending colon. We performed an emergency laparoscopy, which revealed no signs of perforation or bowl ischemia but showed air bubbles in the mesentery along the ascending colon. Subsequent endoscopy revealed unclassified inflammatory bowel disease manifesting in the rectum, erythematous mucosa and epithelialized erosions of the stomach. The patient discharged himself on Day 8 after the surgery. The causes of SIP are unknown, but some authors assume microperforation. SIP can be a challenge for the choice of therapy. Laparoscopy may be particularly beneficial in patients with generalized peritonitis, while patients with moderate symptoms may benefit from conservative treatment.

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