銀ナノ粒子の腫瘍壊死因子αが誘導する細胞応答に与える影響

早大学位記番号:新8280早稲田大

Anemia Of Chronic Disease And Kidney Failure

Anemia is a disease that caused due to inflammation, autoimmune disease, or chronic disease as cancer, kidney failure, heart failure, diabetes, but the main reason of anemia is iron deficiency. Breathlessness, weakness, and exhaustion are all possible effects of anemia. Anemia comes in a variety of types. Everyone has a unique reason. Anemia may be chronic or transient. It could be minor or really serious. Anemia may indicate a more serious medical condition.  In this research we will explain the anemia due to chronic disease especially kidney failure. Anemia occurs when decreasing the number of red blood cells that carry oxygen to the body. According to world health organization (WHO), the person has anemia when hemoglobin (which is present in red blood cells, transports oxygen from the lungs to every other organ in the body), (Hb) levels <12.0 g/dl in women and <13.0 g/dl in men. We can treat anemia by iron supplement, medications, blood transfusion, vitB12, blood and bone transplant but it occur in hospital and by healthy diet. If anemia remained untreated it will be a risk of irregular heartbeat, heart failure, infection, and in children it may cause developmental delay. We can diagnosis anemia by blood tests which are used by medical practitioners to look for indications of inflammation-related anemia, other anemias, or other health issues. You will give blood to a medical professional who will then submit the sample to a lab for analysis. The National institutes of health (NIH) approved that we can examine a variety of components and characteristics of your blood, such as how many red blood cells ,the dimensions of red blood cells ,how much hemoglobin is present in your blood and red blood cells ,the quantity of reticulocytes, or growing red blood cells, in your blood. Blood tests are another tool that a medical expert may use to measure how much iron is stored in blood, transferrin, and ferritin. If the results of a blood test indicate that you have anemia low blood iron levels will appear, determining the amount of iron in low and normal range. Adults who suffer from severe anemia may become vulnerable to heart or lung issues. For instance, you might experience heart failure, in which the heart is unable to pump enough blood throughout your body at the proper pressure or tachycardia, which is an unusually rapid heartbeat. Anemia  can also come from obesity unlike exception of some people so we should follow health diet has iron supplement such as meat, sugar beet

Silver nanoparticles reduce the apoptosis induced by tumor necrosis factor-α

Silver nanoparticles (AgNPs) are widely known to have anti-inflammatory properties, but the exact mechanism underlying this anti-inflammatory effect is not clearly understood. Tumor necrosis factor-α (TNFα) is a major pro-inflammatory cytokine that is expressed in the early stage of cell inflammation and induces apoptosis by several known pathways. Our study aimed to investigate the effect of AgNPs on the response of lung epithelial cells to TNFα and the molecular mechanism of this response. Lung epithelial cell line NCI-H292 cells were exposed to AgNPs (5 µg/mL) and/or TNFα (20 ng/mL) for 24 h, then cellular uptake was analyzed using flow cytometry. Our results showed that AgNPs were taken up by cells in a dose-dependent manner and that the cellular uptake ratio of AgNPs was significantly increased in the presence of TNFα. Apoptosis assays indicated that exposure to AgNPs significantly decreased the apoptotic effect of TNFα. Confocal microscopy was used to localize the tumor necrosis factor receptor 1 (TNFR1) and revealed that TNFR1 localized on the surface of cells exposed to TNFα. In contrast, TNFR1 localized inside cells exposed to both AgNPs and TNFα, with very few receptors scattered on the cell membrane. The results indicated that AgNPs reduced the cell surface TNFR1 expression level. The results suggested that the reduction of surface TNFR1 reduced cellular response to TNFα, resulting in an anti-apoptotic effect

Size-Dependent Effect of Silver Nanoparticles on the Tumor Necrosis Factor α-Induced DNA Damage Response

Silver nanoparticles (AgNPs) are widely used in many consumer products due to their anti-inflammatory properties. Therefore, the effect of exposure to AgNPs should be investigated in diseased states in addition to healthy ones. Tumor necrosis factor-α (TNFα) is a major cytokine that is highly expressed in many diseased conditions, such as inflammatory diseases, sepsis, and cancer. We investigated the effects of two different sizes of AgNPs on the TNFα-induced DNA damage response. Cells were exposed to 10 and 200 nm AgNPs separately and the results showed that the 200 nm AgNPs had a lower cytotoxic effect with a higher percent of cellular uptake compared to the 10 nm AgNPs. Moreover, analysis of reactive oxygen species (ROS) generation and DNA damage indicated that TNFα-induced ROS-mediated DNA damage was reduced by 200 nm AgNPs, but not by 10 nm AgNPs. Tumor necrosis factor receptor 1 (TNFR1) was localized on the cell surface after TNFα exposure with or without 10 nm AgNPs. In contrast, the expression of TNFR1 on the cell surface was reduced by the 200 nm AgNPs. These results suggested that exposure of cells to 200 nm AgNPs reduces the TNFα-induced DNA damage response via reducing the surface expression of TNFR1, thus reducing the signal transduction of TNFα

Silver nanoparticles reduce the apoptosis induced by tumor necrosis factor-α

<p>Silver nanoparticles (AgNPs) are widely known to have anti-inflammatory properties, but the exact mechanism underlying this anti-inflammatory effect is not clearly understood. Tumor necrosis factor-α (TNFα) is a major pro-inflammatory cytokine that is expressed in the early stage of cell inflammation and induces apoptosis by several known pathways. Our study aimed to investigate the effect of AgNPs on the response of lung epithelial cells to TNFα and the molecular mechanism of this response. Lung epithelial cell line NCI-H292 cells were exposed to AgNPs (5 µg/mL) and/or TNFα (20 ng/mL) for 24 h, then cellular uptake was analyzed using flow cytometry. Our results showed that AgNPs were taken up by cells in a dose-dependent manner and that the cellular uptake ratio of AgNPs was significantly increased in the presence of TNFα. Apoptosis assays indicated that exposure to AgNPs significantly decreased the apoptotic effect of TNFα. Confocal microscopy was used to localize the tumor necrosis factor receptor 1 (TNFR1) and revealed that TNFR1 localized on the surface of cells exposed to TNFα. In contrast, TNFR1 localized inside cells exposed to both AgNPs and TNFα, with very few receptors scattered on the cell membrane. The results indicated that AgNPs reduced the cell surface TNFR1 expression level. The results suggested that the reduction of surface TNFR1 reduced cellular response to TNFα, resulting in an anti-apoptotic effect.</p

Green Synthetized Selenium Nanoparticles Using <i>Syzygium aromaticum</i> (Clove) Extract Reduce Pentylenetetrazol-Induced Epilepsy and Associated Cortical Damage in Rats

We aimed to investigate the potential anticonvulsant effect of green synthetized selenium nanoparticles (SeNPs) using Syzygium aromaticum extract (SAE) (SAE-SeNPs) against epileptic seizures and cortical damage induced by pentylenetetrazole (PTZ) injection in rats and its mechanism. A total of 84 rats were divided into six groups; control, PTZ-exposed group, SAE + PTZ-treated group, sodium selenite (Na2SeO3) + PTZ-treated group, SAE-SeNPs + PTZ-treated group, and diazepam + PTZ-treated group. SAE-SeNPs significantly increase (p p p p < 0.05) the PTZ-induced changes in the neurotransmitter norepinephrine level and acetylcholinesterase enzymatic activity. These data concluded the anticonvulsant activity of SAE-SeNPs via their antioxidant, anti-inflammatory, and anti-apoptotic effects, along with their ability to modulate neurotransmitters