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1.
PLoS One ; 15(2): e0228895, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32032388

RESUMO

BACKGROUND: Alpha-1-antitrypsin is a protein involved in avoidance of different processes that are seen in diabetic retinopathy pathogenesis. These processes include apoptosis, extracellular matrix remodeling and damage of vessel walls and capillaries. Furthermore, because of its anti-inflammatory effects, alpha-1-antitrypsin has been proposed as a possible therapeutic approach for diabetic retinopathy. Our group tested alpha-1-antitrypsin in a type 1 diabetes mouse model and observed a reduction of inflammation and retinal neurodegeneration. Thus, shedding light on the mechanism of action of alpha-1-antitrypsin at molecular level may explain how it works in the diabetic retinopathy context and show its potential for use in other retinal diseases. METHODS: In this work, we evaluated alpha-1-antitrypsin in an ARPE-19 human cell line exposed to high glucose. We explored the expression of different mediators on signaling pathways related to pro-inflammatory cytokines production, glucose metabolism, epithelial-mesenchymal transition and other proteins involved in the normal function of retinal pigment epithelium by RT-qPCR and Western Blot. RESULTS: We obtained different expression patterns for evaluated mediators altered with high glucose exposure and corrected with the use of alpha-1-antitrypsin. CONCLUSIONS: The expression profile obtained in vitro for the evaluated proteins and mRNA allowed us to explain our previous results obtained on mouse models and to hypothesize how alpha-1-antitrypsin hinder diabetic retinopathy progression on a complex network between different signaling pathways. GENERAL SIGNIFICANCE: This network helps to understand the way alpha-1-antitrypsin works in diabetic retinopathy and its scope of action.


Assuntos
Retinopatia Diabética/metabolismo , alfa 1-Antitripsina/metabolismo , alfa 1-Antitripsina/fisiologia , Animais , Apoptose/efeitos dos fármacos , Linhagem Celular , Retinopatia Diabética/patologia , Modelos Animais de Doenças , Glucose/metabolismo , Humanos , Inflamação/metabolismo , Camundongos , NF-kappa B/metabolismo , Retina/metabolismo , Epitélio Pigmentado da Retina/metabolismo , Epitélio Pigmentado da Retina/fisiologia , Transdução de Sinais/efeitos dos fármacos , Fator de Necrose Tumoral alfa/metabolismo
2.
Curr Eye Res ; 43(4): 466-473, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-29265937

RESUMO

PURPOSE: The objective is to analyze the antiangiogenic mechanism of suramab, a pharmaceutical compound of bevacizumab and suramin, in a rabbit model of corneal angiogenesis. MATERIAL AND METHODS: Corneal neovascularization was induced in four groups of six New Zealand White rabbits by applying a filter paper disk soaked in 1 M Na (OH) on the central cornea. Group one was treated after injury with intravenous suramab at a dose equivalent to 3 mg/kg of bevacizumab and 10 mg/kg of suramin. Group two was treated with intravenous bevacizumab (5 mg/kg). Group three was treated with 10 mg/kg of suramin while the control group received no treatment. Digital photographs were taken at days 9, 15, 21, and 35. Neovessel formation was quantified giving a 0-4 score to each quadrant according to the centripetal growth of the longest vessel (neovessel index, NVI). Animals were sacrificed at day 35. Corneas were processed for histology, immunohistochemistry, and Western-blot using primary antibodies against P2X2, basic fibroblast growth factor (bFGF), LYVE-1, PECAM-1, and vascular endothelial growth factor-A (VEGF-A). RESULTS: Suramab significantly reduced neovessel growth (mean NVI: 4.2) compared to bevacizumab (8.4), suramin (7.22), and control animals (12.2) at 35 days post-injury (p < 0.01). A lower protein expression of P2X2, bFGF, LYVE-1, PECAM-1, and VEGF-A was found in the cornea of suramab animals than in the other groups of animals. CONCLUSIONS: Joint downregulation of bFGF, P2X2, bFGF, and LYVE-1 constitutes a mechanism that induces greater and longer inhibition of corneal angiogenesis. Results might be relevant to ophthalmic care. Ocular administration of suramab is currently being investigated.


Assuntos
Bevacizumab/farmacologia , Córnea/patologia , Neovascularização da Córnea/tratamento farmacológico , Regulação para Baixo/efeitos dos fármacos , Fator 2 de Crescimento de Fibroblastos/biossíntese , Receptores Purinérgicos P2X2/biossíntese , Suramina/farmacologia , Animais , Western Blotting , Córnea/metabolismo , Neovascularização da Córnea/metabolismo , Neovascularização da Córnea/patologia , Modelos Animais de Doenças , Combinação de Medicamentos , Imuno-Histoquímica , Coelhos
3.
Rev. salud pública ; 15(1): 129-137, ene.-feb. 2013. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-703428

RESUMO

Lograr la certificación de la discapacidad en Colombia ha sido un reto que las personas con discapacidad se han impuesto y que el país ha asumido, en el marco de la legislación vigente y de los acuerdos internacionales a los que ha adherido Colombia. Para el efecto, se ha adoptado el modelo de clasificación internacional del funcionamiento, la discapacidad y la salud (CIF), en razón a que este instrumento, validado internacionalmente en diversos estudios, permite incorporar un estándar internacional de evaluación del estado funcional de los individuos. En este ensayo, inicialmente se define el concepto "discapacidad" y se ubica en el contexto histórico que lo precede, hasta llegar a la actual estructura de dominios y categorías de la CIF, instrumento que proporciona un marco común y generalizado, de forma tal que se permita proporcionar una adecuada asignación de servicios y beneficios generales, específicos, y a la vez se evalúa el diferencial existente entre el funcionamiento real y el potencial de las personas con discapacidad.


Certifying disability in Colombia has been demanded by disabled people; the country has assumed such challenge within the frame work of current legislation and international agreements signed by Colombia. A model of international classification of functioning (ICF), disability and healthwas thus adopted as it has been validated internationally in several studies; it incorporates international standards thereby allowing reliable evaluation of individuals' functional status. This essayinitially defines the concept of disabilityand locates it within a historical context leading to current ICF domain structure and categories. Such instrument provides a common, wide-ranging framework for providing suitable allocation of services and general and specific benefits, while assessing the differential between disabled people's current performance and their potential.


Assuntos
Humanos , Avaliação da Deficiência , Pessoas com Deficiência , Classificação Internacional de Funcionalidade, Incapacidade e Saúde , Controle Social Formal , Colômbia
4.
Arch Neurol ; 68(12): 1587-90, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22159057

RESUMO

OBJECTIVE: To describe a case of propylthiouracil-induced lupus, complicated with antiphospholipid syndrome and acute ischemic stroke. DESIGN: Case report. SETTING: Academic medical center. PATIENT: A 27-year-old man with a diagnosis of Graves disease developed multiple ischemic strokes 2 weeks after starting treatment with propylthiouracil. Thyrotoxicosis and abnormal hypercoagulable and rheumatological profiles were remarkable, with prolonged partial thromboplastin time, elevated anticardiolipin antibody level, and positive antinuclear antibody, lupus anticoagulant, Sjögren antibody, and anti-double-stranded DNA antibody test results, which were more than 8-fold greater than normal values. No clinical manifestations of systemic lupus erythematosus were present. INTERVENTION: Discontinuation of propylthiouracil and treatment with radioactive iodine. RESULTS: Hyperthyroidism resolved and anti-double-stranded DNA antibodies returned to normal levels. Eventually, antiphospholipid syndrome was diagnosed. He was treated with oral anticoagulation and remained asymptomatic for 1 year of follow-up. CONCLUSION: In this young man with Graves hyperthyroidism, treatment with propylthiouracil was associated with transient autoimmune reactions suggestive of drug-induced lupus, antiphospholipid syndrome, and acute ischemic stroke.


Assuntos
Síndrome Antifosfolipídica/induzido quimicamente , Antitireóideos/efeitos adversos , Isquemia Encefálica/induzido quimicamente , Propiltiouracila/efeitos adversos , Acidente Vascular Cerebral/induzido quimicamente , Adulto , Seguimentos , Doença de Graves/tratamento farmacológico , Doença de Graves/radioterapia , Humanos , Lúpus Eritematoso Sistêmico/induzido quimicamente , Masculino , Propiltiouracila/uso terapêutico
5.
Neurology ; 70(13): 1049-51, 2008 Mar 25.
Artigo em Inglês | MEDLINE | ID: mdl-18362285
6.
Quintessence Int ; 34(7): 509-14, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-12946069

RESUMO

Dental invagination or dens in dente is a rare malformation with a widely varied morphology. Radiographically, the affected tooth shows an infolding of the enamel and dentin that can extend to within the pulp cavity and the root and sometimes to the root apex. It can occur in both primary and permanent teeth, and its prevalence is reported to be 1.7% to 10%. The dental anomalies observed in association with dental invagination include taurodontia, microdontia, supernumerary teeth, gemination, and dentinogenesis imperfecta. This article presents a clinical case in which a radiographic finding could be compatible with the presence of a nasopalatine or globulomaxillary cyst and a dens in dente. It was decided to extract the invaginated tooth, and by 15 days postextraction, the radiolucid area had completely disappeared. The complex surgery that would have been required to remove the patient's supposed cyst was thus avoided. Clinical and radiographic examination is suggested before making further decisions that could complicate treatment when a lesion is associated with other dental anomalies.


Assuntos
Dens in Dente/complicações , Doenças Maxilares/complicações , Cistos não Odontogênicos/complicações , Criança , Dens in Dente/cirurgia , Feminino , Humanos , Doenças Maxilares/terapia , Cistos não Odontogênicos/terapia , Indução de Remissão , Extração Dentária
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