3 research outputs found
Detection of brain stroke in the MRI image using FPGA
One of the most important difficulties which doctors face in diagnosing is the analysis and diagnosis of brain stroke in magnetic resonance imaging (MRI) images. Brain stroke is the interruption of blood flow to parts of the brain that causes cell death. To make the diagnosis easier for doctors, many researchers have treated MRI images with some filters by using Matlab program to improve the images and make them more obvious to facilitate diagnosis by doctors. This paper introduces a digital system using hardware concepts to clarify the brain stroke in MRI image. Field programmable gate arrays (FPGA) is used to implement the system which is divided into four phases: preprocessing, adjust image, median filter, and morphological filters alternately. The entire system has been implemented based on Zynq FPGA evaluation board. The design has been tested on two MRI images and the results are compared with the Matlab to determine the efficiency of the proposed system. The proposed hardware system has achieved an overall good accuracy compared to Matlab where it ranged between 90.00% and 99.48%
Procoagulant Extracellular Vesicles Alter Trophoblast Differentiation inMice by a Thrombo-InflammatoryMechanism
Procoagulant extracellular vesicles (EV) and platelet activation have been associated
with gestational vascular complications. EV-induced platelet-mediated placental inflammasome
activation has been shown to cause preeclampsia-like symptoms in mice. However, the effect of
EV-mediated placental thrombo-inflammation on trophoblast differentiation remains unknown. Here,
we identify that the EV-induced thrombo-inflammatory pathway modulates trophoblast morphology
and differentiation. EVs and platelets reduce syncytiotrophoblast differentiation while increasing
giant trophoblast and spongiotrophoblast including the glycogen-rich cells. These effects are plateletdependent
and mediated by the NLRP3 inflammasome. In humans, inflammasome activation was
negatively correlated with trophoblast differentiation marker GCM1 and positively correlated with
blood pressure. These data identify a crucial role of EV-induced placental thrombo-inflammation on
altering trophoblast differentiation and suggest platelet activation or inflammasome activation as a
therapeutic target in order to achieve successful placentation
Neutrophil Extracellular Traps Promote NLRP3 Inflammasome Activation and Glomerular Endothelial Dysfunction in Diabetic Kidney Disease
Diabetes mellitus is a metabolic disease largely due to lifestyle and nutritional imbalance, resulting in insulin resistance, hyperglycemia and vascular complications. Diabetic kidney disease (DKD) is a major cause of end-stage renal failure contributing to morbidity and mortality worldwide. Therapeutic options to prevent or reverse DKD progression are limited. Endothelial and glomerular filtration barrier (GFB) dysfunction and sterile inflammation are associated with DKD. Neutrophil extracellular traps (NETs), originally identified as an innate immune mechanism to combat infection, have been implicated in sterile inflammatory responses in non-communicable diseases. However, the contribution of NETs in DKD remains unknown. Here, we show that biomarkers of NETs are increased in diabetic mice and diabetic patients and that these changes correlate with DKD severity. Mechanistically, NETs promote NLRP3 inflammasome activation and glomerular endothelial dysfunction under high glucose stress in vitro and in vivo. Inhibition of NETs (PAD4 inhibitor) ameliorate endothelial dysfunction and renal injury in DKD. Taken together, NET-induced sterile inflammation promotes diabetes-associated endothelial dysfunction, identifying a new pathomechanism contributing to DKD. Inhibition of NETs may be a promising therapeutic strategy in DKD