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1.
J Am Soc Nephrol ; 27(10): 3117-3128, 2016 10.
Artículo en Inglés | MEDLINE | ID: mdl-26961347

RESUMEN

Like many organs, the kidney stiffens after injury, a process that is increasingly recognized as an important driver of fibrogenesis. Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ) are related mechanosensory proteins that bind to Smad transcription factors, the canonical mediators of profibrotic TGF-ß responses. Here, we investigated the role of YAP/TAZ in the matrix stiffness dependence of fibroblast responses to TGF-ß In contrast to growth on a stiff surface, fibroblast growth on a soft matrix led to YAP/TAZ sequestration in the cytosol and impaired TGF-ß-induced Smad2/3 nuclear accumulation and transcriptional activity. YAP knockdown or treatment with verteporfin, a drug that was recently identified as a potent YAP inhibitor, elicited similar changes. Furthermore, verteporfin reduced YAP/TAZ levels and decreased the total cellular levels of Smad2/3 after TGF-ß stimulation. Verteporfin treatment of mice subjected to unilateral ureteral obstruction similarly reduced YAP/TAZ levels and nuclear Smad accumulation in the kidney, and attenuated renal fibrosis. Our data suggest that organ stiffening cooperates with TGF-ß to induce fibrosis in a YAP/TAZ- and Smad2/3-dependent manner. Interference with this YAP/TAZ and TGF-ß/Smad crosstalk likely underlies the antifibrotic activity of verteporfin. Finally, through repurposing of a clinically used drug, we illustrate the therapeutic potential of a novel mechanointerference strategy that blocks TGF-ß signaling and renal fibrogenesis.


Asunto(s)
Proteínas Adaptadoras Transductoras de Señales/fisiología , Riñón/patología , Fosfoproteínas/fisiología , Proteína Smad2/fisiología , Proteína smad3/fisiología , Factores de Transcripción/fisiología , Factor de Crecimiento Transformador beta/fisiología , Aciltransferasas , Animales , Proteínas de Ciclo Celular , Fibrosis/etiología , Masculino , Ratones , Ratones Endogámicos C57BL , Transducción de Señal , Proteínas Señalizadoras YAP
2.
Ir J Med Sci ; 193(1): 509-516, 2024 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-37365446

RESUMEN

BACKGROUND: Acute retinal necrosis (ARN) is a progressive necrotizing retinitis caused by viral infection. Optimal management strategies have not been established for this detrimental disease. Previous literature published suggests that Varicella-zoster virus (VZV) and Herpes simplex virus-1 (HSV1) are the most common promoters of acute retinal necrosis (ARN). AIMS: The purpose of our study was to investigate the viral distribution, demographic, and treatment outcomes of ARN. METHODS: A retrospective chart review evaluated data from PCR-positive ARN patients diagnosed between 2009 and 2018. RESULTS: Analysis of fourteen eyes from 12 patients found CMV and VZV as the commonest causes of ARN. Patients on 1 g of valacyclovir three times a day (V1T) had worse vision between first and final visits (mean difference of 1.25 ± 0.65, n = 2) compared with patients treated with 2 g of valacyclovir three times a day (V2T), or 900 mg twice a day of valganciclovir (V9B) (mean difference of - 0.067 ± 0.13, n = 6, and 0.067 ± 0.067, n = 6, respectively). Both V1T patients developed retinal detachments (RD). Both CMV patients treated with intravitreal triamcinolone developed ARN, elevated IOP, and one developed multiple RD. CONCLUSIONS: Our review found increased incidence of CMV-positive ARN. Patients with zone 1 disease had worse initial visual acuity. Moreover, patients had more favorable outcomes with V2T and V9B compared to V1T. CMV-positive patients clinically worsened after intravitreal steroid injections, further underscoring the value of a PCR diagnosis to tailor the patients' treatment plan accordingly.


Asunto(s)
Infecciones por Citomegalovirus , Desprendimiento de Retina , Síndrome de Necrosis Retiniana Aguda , Humanos , Síndrome de Necrosis Retiniana Aguda/diagnóstico , Síndrome de Necrosis Retiniana Aguda/etiología , Valaciclovir , Estudios Retrospectivos , Herpesvirus Humano 3/genética , Resultado del Tratamiento , Reacción en Cadena de la Polimerasa , Infecciones por Citomegalovirus/complicaciones
3.
Retin Cases Brief Rep ; 14(2): 170-173, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-29176535

RESUMEN

PURPOSE: To describe a case of spontaneous improvement of syphilis chorioretinitis and review the literature. METHODS: Case report and literature review of cases with untreated syphilis chorioretinitis. RESULTS: A 58-year-old man presented to the emergency department with counting fingers vision, normal fundus, and disruption of the outer retinal layers on optical coherence tomography of the right eye. Examination by a retina specialist 3 weeks later revealed visual acuity of 20/50 and partial restoration of outer retinal layers on optical coherence tomography. Workup showed positive serology for syphilis and human immunodeficiency virus. Treatment with intravenous penicillin resulted in further vision improvement. Literature review showed six cases of spontaneous improvement of syphilis chorioretinitis. CONCLUSION: Spontaneous improvement of syphilis chorioretinitis is possible. Clinicians should keep a high index of suspicion and consider syphilis chorioretinitis in diseases that affect the outer retina even with spontaneous improvement.


Asunto(s)
Coriorretinitis/diagnóstico , Coroides/patología , Infecciones Bacterianas del Ojo/diagnóstico , Retina/patología , Sífilis/diagnóstico , Agudeza Visual , Angiografía con Fluoresceína , Estudios de Seguimiento , Fondo de Ojo , Humanos , Masculino , Persona de Mediana Edad , Remisión Espontánea , Tomografía de Coherencia Óptica/métodos
4.
Nutrients ; 9(4)2017 Mar 31.
Artículo en Inglés | MEDLINE | ID: mdl-28362355

RESUMEN

Individuals living with metabolic syndrome (MetS) such as diabetes and obesity are at high risk for developing chronic kidney disease (CKD). This study investigated the beneficial effect of whole grape powder (WGP) diet on MetS-associated CKD. Obese diabetic ZSF1 rats, a kidney disease model with MetS, were fed WGP (5%, w/w) diet for six months. Kidney disease was determined using blood and urine chemical analyses, and histology. When compared to Vehicle controls, WGP intake did not change the rat bodyweight, but lowered their kidney, liver and spleen weight, which were in parallel with the lower serum glucose and the higher albumin or albumin/globin ratio. More importantly, WGP intake improved the renal function as urination and proteinuria decreased, or it prevented kidney tissue damage in these diabetic rats. The renal protection of WGP diet was associated with up-regulation of antioxidants (Dhcr24, Gstk1, Prdx2, Sod2, Gpx1 and Gpx4) and downregulation of Txnip (for ROS production) in the kidneys. Furthermore, addition of grape extract reduced H2O2-induced cell death of cultured podocytes. In conclusion, daily intake of WGP reduces the progression of kidney disease in obese diabetic rats, suggesting a protective function of antioxidant-rich grape diet against CKD in the setting of MetS.


Asunto(s)
Antioxidantes/uso terapéutico , Diabetes Mellitus Tipo 2/complicaciones , Nefropatías Diabéticas/dietoterapia , Suplementos Dietéticos , Preparaciones de Plantas/uso terapéutico , Insuficiencia Renal Crónica/dietoterapia , Vitis/química , Animales , Antioxidantes/aislamiento & purificación , Antioxidantes/metabolismo , Biomarcadores/sangre , Biomarcadores/orina , Línea Celular , Cruzamientos Genéticos , Nefropatías Diabéticas/complicaciones , Nefropatías Diabéticas/metabolismo , Nefropatías Diabéticas/fisiopatología , Progresión de la Enfermedad , Frutas/química , Regulación de la Expresión Génica , Riñón/metabolismo , Riñón/patología , Riñón/fisiopatología , Masculino , Síndrome Metabólico/complicaciones , Ratones , Tamaño de los Órganos , Estrés Oxidativo , Preparaciones de Plantas/aislamiento & purificación , Preparaciones de Plantas/metabolismo , Podocitos/metabolismo , Podocitos/patología , Distribución Aleatoria , Ratas Endogámicas SHR , Ratas Zucker , Insuficiencia Renal Crónica/complicaciones , Insuficiencia Renal Crónica/metabolismo , Insuficiencia Renal Crónica/fisiopatología
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