Link between Intestinal CD36 Ligand Binding and Satiety Induced by a High Protein Diet in Mice

CD36 is a ubiquitous membrane glycoprotein that binds long-chain fatty acids. The presence of a functional CD36 is required for the induction of satiety by a lipid load and its role as a lipid receptor driving cellular signal has recently been demonstrated. Our project aimed to further explore the role of intestinal CD36 in the regulation of food intake. Duodenal infusions of vehicle or sulfo-N-succinimidyl-oleate (SSO) was performed prior to acute infusions of saline or Intralipid (IL) in mice. Infusion of minute quantities of IL induced a decrease in food intake (FI) compared to saline. Infusion of SSO had the same effect but no additive inhibitory effect was observed in presence of IL. No IL- or SSO-mediated satiety occurred in CD36-null mice. To determine whether the CD36-mediated hypophagic effect of lipids was maintained in animals fed a satietogen diet, mice were subjected to a High-Protein diet (HPD). Concomitantly with the satiety effect, a rise in intestinal CD36 gene expression was observed. No satiety effect occurred in CD36-null mice. HPD-fed WT mice showed a diminished FI compared to control mice, after saline duodenal infusion. But there was no further decrease after lipid infusion. The lipid-induced decrease in FI observed on control mice was accompanied by a rise in jejunal oleylethanolamide (OEA). Its level was higher in HPD-fed mice than in controls after saline infusion and was not changed by lipids. Overall, we demonstrate that lipid binding to intestinal CD36 is sufficient to produce a satiety effect. Moreover, it could participate in the satiety effect induced by HPD. Intestine can modulate FI by several mechanisms including an increase in OEA production and CD36 gene expression. Furthermore, intestine of mice adapted to HPD have a diminished capacity to modulate their food intake in response to dietary lipids

Extraction of pure components from overlapped signals in gas chromatography-mass spectrometry (GC-MS)

Gas chromatography-mass spectrometry (GC-MS) is a widely used analytical technique for the identification and quantification of trace chemicals in complex mixtures. When complex samples are analyzed by GC-MS it is common to observe co-elution of two or more components, resulting in an overlap of signal peaks observed in the total ion chromatogram. In such situations manual signal analysis is often the most reliable means for the extraction of pure component signals; however, a systematic manual analysis over a number of samples is both tedious and prone to error. In the past 30 years a number of computational approaches were proposed to assist in the process of the extraction of pure signals from co-eluting GC-MS components. This includes empirical methods, comparison with library spectra, eigenvalue analysis, regression and others. However, to date no approach has been recognized as best, nor accepted as standard. This situation hampers general GC-MS capabilities, and in particular has implications for the development of robust, high-throughput GC-MS analytical protocols required in metabolic profiling and biomarker discovery. Here we first discuss the nature of GC-MS data, and then review some of the approaches proposed for the extraction of pure signals from co-eluting components. We summarize and classify different approaches to this problem, and examine why so many approaches proposed in the past have failed to live up to their full promise. Finally, we give some thoughts on the future developments in this field, and suggest that the progress in general computing capabilities attained in the past two decades has opened new horizons for tackling this important problem

Solubilization of delta12- and delta6-desaturases from seeds of borage microsomes

International audienc

Behaviour and fate of urban particles in coastal waters: Settling rate, size distribution and metals contamination characterization

The evaluation of contaminant net fluxes from the coast to the open sea requires the study of terrigeneous particles behaviour and fate. We studied the particles issued from two small coastal rivers whose waters are mixed with treated wastewater (TWW) coming from the Marseille wastewater treatment plant (WWTP) just before discharge to the Mediterranean Sea. An experimental device was developed and used to investigate particles settling rates, size distribution and metallic contamination when mixing with seawater. The particles were sampled in flood deposits of rivers and outlets during rainy periods and in the outlet water during dry periods. The flood deposits were mainly composed of 50–200 μm-sized particles, higher metals content being observed in the finest fractions. Dry period particles showed the stronger influence of wastewater inputs. Al, Ca, Cs, Li, Rb, Ti, and Tl were mainly of terrigeneous origin, whereas Ag, Ba, Cd, Cr, Cu, Hg, Mg, Mo, Ni, Pb, POC, Sb, Sn and Zn were of anthropogenic origin, issued from non-treated sewage, TWW or industrial waste. In seafloor sediments, all metals exhibited a continuous increase of concentration from the outlet to, at least, 800 m offshore. Implementation of settling particles characteristics in a 3D hydrodynamic and sediment transport model reproduced well the observed deposition of polluted particles in the coastal zone and indicated a non-negligible offshore export of the finest particles and their accompanying pollutants

Métabolisme des annexes hydrauliques des corridors hydro-écologiques – des casiers Girardon du Rhône aux gravières de la Bassée.

National audienc

Indicators of terrestrial biogenic hydrocarbon contamination and linear alkyl benzenes as land-base pollution tracers in marine sediments

International audienceAliphatics (n-alkanes) and polycyclic aromatic hydrocarbons (PAHs) were measured in surface sediments collected from 12 sampling points (P1-P12) of sewage discharge to the sea from the wastewater treatment plant of Cortiou (France). Total n-alkanes and PAHs concentrations ranged from 34 to 2,155 and 696 to 10,700 mu g kg(-1), respectively. Some specific hydrocarbon indexes suggested that terrestrial biogenic inputs are predominant compared to marine sources and that pyrolytic sources derived from wood and biomass combustion contribute to PAHs in the surface sediments. Total linear alkyl benzenes in Cortiou sediments ranged from 42.9 to 502.3 mu g kg(-1). Low internal and external (I/E) isomers ratio (P0) suggests that inadequately treated sewage is discharged into the marine environment while some environmental processes might change I/E ratios during transport seaward (P1-P12). The high contaminant levels followed by the cumulative concentration of several compounds may lead to elevated toxicity levels in the sediments