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1.
J Cereb Blood Flow Metab ; 43(6): 843-855, 2023 06.
Artículo en Inglés | MEDLINE | ID: mdl-36703604

RESUMEN

CD36 expressed in multiple cell types regulates inflammation, vascular function, and innate immunity. Specifically, CD36 in microvascular endothelial cells (ECs) signals to elicit inflammation and causes EC death. This study investigated roles for EC-CD36 on acute stroke pathology in normal and obese conditions. Obesity induced by a high-fat diet (HD) selectively increased CD36 expression in ECs, not in monocytes/macrophages, in the post-ischemic brain. Mice deficient CD36 in ECs (ECCD36-/-) showed reduced injury size and vascular permeability in normal conditions. While control mice fed a HD developed obesity and aggravated stroke injury, ECCD36-/- mice were resistant to develop an obesity phenotype. Subjecting ECCD36-/- mice to stroke resulted in reduced injury size and BBB disruption. Moreover, the mice had reduced MCP-1 and CCR2 gene expression, resulting in reduced monocyte trafficking with improved survival and acute motor function. Reduced MCP-1 and CCR2 expression was still evident in ECCD36-/- mice subjected to severe stroke, suggesting that monocyte trafficking is an infarct-independent metabolic effect associated with specific EC-CD36 deletion. Our findings demonstrate the importance of EC-CD36 in developing vascular comorbidities and suggest that targeting EC-CD36 is a potential preventative strategy to normalize vascular risk factors, leading to improved acute stroke outcomes.


Asunto(s)
Lesiones Encefálicas , Accidente Cerebrovascular , Ratones , Animales , Monocitos/metabolismo , Células Endoteliales/metabolismo , Accidente Cerebrovascular/patología , Lesiones Encefálicas/metabolismo , Inflamación/patología , Obesidad/complicaciones , Obesidad/metabolismo , Ratones Endogámicos C57BL
2.
Natl Med J India ; 36(2): 95-96, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-38692598

RESUMEN

Prolonged fever with pancytopenia and hepatosplenomegaly is a clinical entity frequently encountered by physicians. The diagnosis of such cases is challenging due to the diversity of differential diagnoses. Hepatosplenic T-cell lymphoma is a rare and aggressive type of non-Hodgkin lymphoma that can present with massive hepatosplenomegaly, pancytopenia and prolonged fever. Most of the patients are young men and the majority are associated with chronic immunosuppression. We report a 40-year-old immunocompetent woman with prolonged fever and pancytopenia due to hepatosplenic T-cell lymphoma.


Asunto(s)
Fiebre , Hepatomegalia , Linfoma de Células T , Pancitopenia , Esplenomegalia , Humanos , Pancitopenia/etiología , Pancitopenia/diagnóstico , Adulto , Femenino , Esplenomegalia/etiología , Hepatomegalia/etiología , Fiebre/etiología , Linfoma de Células T/complicaciones , Linfoma de Células T/diagnóstico , Linfoma de Células T/patología , Neoplasias del Bazo/complicaciones , Neoplasias del Bazo/diagnóstico , Neoplasias Hepáticas/complicaciones , Neoplasias Hepáticas/diagnóstico , Diagnóstico Diferencial
4.
Mov Disord Clin Pract ; 8(1): 133-134, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-36989011
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