Abstract
Aim: Chronic inflammation of adipose tissues plays a key role in obesity-induced metabolic disorders. We examined effects of sera from obese patients with or without different compositions of metabolic disorders on the activation of Toll-like receptor 4 (TLR4)/nuclear factor-kappa B (NF-κB) signaling pathway in the human monocytic leukemia cell line (THP-1), which have never been reported. Methods: With or without pretreatment of TLR4 monoclonal antibody, THP-1 cells were incubated for 48h by sera from 45 obese patients with or without metabolic disorders and 15 controls. The level of TLR4 in THP-1 cells, intracellular level of phosphorylated NF-κB p65, IL-1β and TNF-α levels in cell culture supernatants were measured. Results: Compared with controls, the expression level of TLR4, NF-κB p65, IL-1β and TNF-α were significantly increased (p <0.05) after cells were incubated with sera from obese patients. The more compositions of metabolic disorders , the higher increase of these factors. Pretreatment with TLR4 monoclonal antibody suppressed the degree of increase in these factors (p <0.05). Conclusions: Sera from obese patient s could induce the activation of TLR4/NF-κB signaling pathway in THP-1 monocytes by different degrees. The TLR4/NF-κB signaling pathway plays an important role in the proinflammatory effect of obese patient-derived sera.
Highlights
In recent years, numerous studies [1,2,3,4] have suggested that for obese patients, the greatest health risk is not fat itself, but rather adipose inflammation
Insulin resistance is an important factor in the development of obesity-related diseases, and it is the driving force for the continuous deterioration observed in individuals afflicted with obesity-related diseases
OTD exhibited significantly higher fasting blood glucose (FBG), 2-h post-prandial blood glucose (2-h PBG), TG, total cholesterol (TC), low-density lipoproteincholesterol (LDL-C), and systolic and diastolic blood pressures (p
Summary
Numerous studies [1,2,3,4] have suggested that for obese patients, the greatest health risk is not fat itself, but rather adipose inflammation. The adipose tissues of obese patients exhibit characteristics of chronic inflammation, and this chronic inflammation of the adipose tissues plays a key role in the occurrence and development of obesity-induced metabolic disorders (e.g., diabetes, and dyslipidemia). Insulin resistance is an important factor in the development of obesity-related diseases, and it is the driving force for the continuous deterioration observed in individuals afflicted with obesity-related diseases. The cause of insulin resistance is very complex and involves a variety of factors. Metabolic inflammation plays a vital role in the pathogenesis of obesity-related vascular complications [2,3]
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