Neutrophil apoptosis and clearance by macrophages are essential for wound healing. Evidence suggests that hyperbaric oxygen (HBO) exposure may enhance neutrophil apoptosis, but HBO effects leading to neutrophil clearance by macrophages are still unclear. In the current study, bovine neutrophils and monocyte-derived macrophages (MDMΦ) were co-cultured under HBO (97.9% O2, 2.1% CO2 at 2.4 atm absolute (ATA)) (1 atm = 101.325 kPa), hyperbaric normoxia (8.8% O2 at 2.4 ATA), normobaric hyperoxia (95% O2, 5% CO2), normoxia (air), and normobaric hypoxia (5% O2, 5% CO2). Phagocytosis of fresh and 22 h aged neutrophils by MDMΦ was increased after HBO pre-treatment, assessed using flow cytometry and light microscopy. Enhanced clearance of neutrophils was accompanied by an increase in H2O2 levels following HBO pre-treatment with upregulation of IL-10 (anti-inflammatory cytokine) mRNA expression in LPS-stimulated MDMΦ that had ingested aged neutrophils. TNF-α (pro-inflammatory cytokine) gene expression did not change in LPS-stimulated MDMΦ that had ingested fresh or aged neutrophils after HBO, pressure, and hyperoxia. These findings suggest that HBO-activated MDMΦ participate in the clearance of apoptotic cells. Uptake of neutrophils by MDMΦ exposed to HBO may contribute to resolution of inflammation, because HBO induced up-regulation of IL-10 mRNA expression.
Background: Ovarian cancer (OC) is the most common cancer and a leading cause of death in women. It well known that suppress the apoptosis initiates tumor and its development. Oxidative stress, and inflammation showed to have a role in tumorigenesis. However, the mechanism still unclear. Methods: 90 females were involved in the current study. Blood samples were obtained from thirty healthy controls, thirty premenopausal women, and thirty postmenopausal women with primary diagnosis of ovarian cancer. Plasma SOD activity was determined by spectrophotometry method, plasma levels of 8-OHG, IL-8, and Cas-8 were measured by ELISA. methylation specific PCR (MSP PCR) was applied for measurements of un-methylation and methylation levels of Cas-8 gene. Result: The results showed a significant decrease in SOD activity in postmenopausal group compared to premenopausal women and control groups (P < 0.05). A significant increase in 8-OHG and IL-8 levels in both OC groups compared with control group (P < 0.05). Apoptosis were decreased through levels of Cas-8 in patients group compared to control group (P< 0.05). Also a high level methylation of Cas-8 gene was observed in plasma sample of patient groups compared to control group. Conclusions: low levels of Cas-8 and methylation of Cas-8 may be involved in OC carcinogenesis and consider as diagnostic marker. Oxidative stress-mediated inflammatory response and methylation of Cas-8, this may be for promoter hyper methylation in OC. Taken together, the result open new sight in strategy therapy for OC.
Objective Obstructive lung diseases (OLD) are chronic inflammatory disorders of the respiratory tract including asthma and chronic obstructive pulmonary disease (COPD). Apo lipoprotein E (Apo E), is a multifunctional protein as it intervenes the binding of lipoproteins or lipid complexes to specific cell-surface receptors. Experimental studies referred to the function of Apo E as an endogenous negative regulator of airway hyper responsiveness and goblet cell hyperplasia. The protective role of Apo E pathways primarily in respiratory disease was explained in human studies and research utilizing experimental murine model systems. Literature data reveal a strong association between redox status, including the enzyme superoxide dismutase (SOD) with both the development a severity of OLD. This study aims to investigate the relation between SOD antioxidant enzyme activity in addition to investigating the level of Apo E and the development of obstructive lung diseases (OLD). Methods Patients with OLD (n = 40) and 40 age-matched healthy controls were enrolled in this study. Serum samples were collected to test the role of Apo E and to test the effect of antioxidant enzyme SOD, and their influence on OLD, all measured by ELISA.Result The results showed a significant decrease in the level of serum SOD activity in patients with OLD when compared with control group (P < 0.05). However, the levels of Apo E did not show a significant difference between the two groups. Conclusion Decreased level of antioxidant SOD suggests the presence of an oxidative stress in asthmatic airways favoring a more oxidative state is present in the airway inflammation. The level of Apo E was non significantly increased in serum of patient, this suggests that protein level of Apo E does not change but may be Apo E gene expression is altered.
Diabetic nephropathy (DN) is the most common and prevalent complication of diabetes mellitus (DM). Persistent hyperglycemia was induced oxidative stress,leading to cell damage and death by apoptosis,and enhanced the development of DN. However,the mechanism by which hyperglycemia induces apoptosis is not well understood. 60 patients (30 patients with Typ2 DM,30 patients with DN) and 30 healthy subjects as control group were enrolled in this study. Serum levels of advanced oxidation protein products (AOPPs) and CAT activity as indirect markers of oxidative stress were measured by the colorimetric method,level of serum caspase-3 as a proapoptotic biomarker was also measured by ELISA. Additionally,expression of the apoptotic genes,nuclear factor-B (NF-κB) in serum was investigated using qPCR. The level of AOPP was significantly increased in DN and DM group than control (P <0.05),while CAT activity in DN significantly decrease (P< 0.05) as compared with DM and control groups. Levels of caspase-3 in DN patients were significantly higher than DM and control groups (𝑃< 0.05),with upregulation of NF-κB mRNA gene expression.This study identified caspase-3 as a final common mediator of high glucose-induced apoptosis and have an important role in DN pathogenesis and progression. Apoptosis seems to be associated with an alteration in inflammatory mediators such as oxidative stress.
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