1.
Systemic and vascular inflammation in an in-vitro model of central obesity.
Ahluwalia, A, Misto, A, Vozzi, F, Magliaro, C, Mattei, G, Marescotti, MC, Avogaro, A, Iori, E
PloS one. 2018;13(2):e0192824
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Plain language summary
Overweight and obesity are major risk factors for a number of chronic diseases, including diabetes, cardiovascular disease and cancer. Obese individuals often have excess fat around the middle, known as central adiposity, a condition known to contribute to an increase in blood levels of compounds such as glycerol and triglycerides. This study builds on a series of studies in which it has been demonstrated that circulation of these compounds reduces glucose uptake and increases lactate availability in all cells. The aim of the study was to challenge the system in-vitro with increasing levels of adiposity to determine the impact this had on compounds in the blood and the extent to which this reflects obesity-related vascular and systemic stress observed in humans. The focus of the study was primarily on lipid-related molecules and pro-inflammatory markers. Visceral adipose tissue was obtained from 9 donors undergoing liver resection for metastatic/benign liver lesions without any underlying chronic liver disease or diabetic complications and body mass index ranging from 20-25. The study outlines that an increase of adiposity in-vitro determines a pro-inflammatory state and results in endothelial stress.
Abstract
Metabolic disorders due to over-nutrition are a major global health problem, often associated with obesity and related morbidities. Obesity is peculiar to humans, as it is associated with lifestyle and diet, and so difficult to reproduce in animal models. Here we describe a model of human central adiposity based on a 3-tissue system consisting of a series of interconnected fluidic modules. Given the causal link between obesity and systemic inflammation, we focused primarily on pro-inflammatory markers, examining the similarities and differences between the 3-tissue model and evidence from human studies in the literature. When challenged with high levels of adiposity, the in-vitro system manifests cardiovascular stress through expression of E-selectin and von Willebrand factor as well as systemic inflammation (expressing IL-6 and MCP-1) as observed in humans. Interestingly, most of the responses are dependent on the synergic interaction between adiposity and the presence of multiple tissue types. The set-up has the potential to reduce animal experiments in obesity research and may help unravel specific cellular mechanisms which underlie tissue response to nutritional overload.
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Separation of cinchona alkaloids, opium alkaloids, heroin, and related narcotics by dynamic-coating high-speed liquid chromaotgraphy.
Wu, CY, Siggia, S, Robinson, T, Waskiewicz, RD
Analytica chimica acta. 1973;63(2):393-402
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Plain language summary
It has already been shown that replacing saturated fatty acids (SFA) with omega 6 (n-6) linoleic acid (LA) can reduce low density lipoproteins (LDL) which is hypothesised to reduce the risk of cardiovascular disease. However, this study looked at the prevention of secondary heart disease and mortality in recovered data from a single-blinded, parallel group, randomised controlled trial carried out between 1966-1973 which replaced dietary SFAs with n-6 polyunsaturated fatty acids (PUFAs) derived from safflower oil. This study also used this recovered data to update their meta-analysis published in 2010. The study was of 458 men who had suffered a recent coronary event and measured mortality over the 7 year period. Results showed a significant reduction in total cholesterol in the intervention group, however, it showed an increase in mortality. The study concluded that the mechanism of cardiovascular disease is independent of cholesterol levels which contradicts traditional understanding and worldwide dietary advice. The updated meta-analysis showed no benefit in replacing SFAs for n-6 or PUFAs for cardiovascular health.