Team 1 : “Nutritional Adaptations, Environment and Diabetes”
Nutritional Adaptations, Environment and Diabetes
To maintain homeostasis in normal range, all living species are able to develop appropriate responses to transient or sustained changes occuring in their direct environment. Humans, all life-long from embryo to elderly, are exposed to environmental modifications including lifestyle changes, nutritional habits or pollutant contaminations. Good health and long-life expectancy are thus strongly dependent on the ability to correctly adapt and respond to these modifications. It is now suspected that metabolic diseases, such as obesity, type 2 diabetes and their related complications, are linked to defects in these adaptive mechanisms.
The main objectives of Team 1 of CarMeN laboratory are to define the mechanisms involved in the physiological response to metabolic stress in humans, to identify potential defects in these processes and to develop new strategies to fight metabolic and nutritional diseases.
Our different research projects combine clinical investigations, studies with animal model and experimental research, based on nutrigenomics and epigenetics. They benefit from the close collaboration of scientists specialized in biochemistry, physiology, immunology, cellular and molecular biology and of clinicians from diabetology, metabolism, nutrition and nephrology.
Our Team is mainly located at the Faculty of Medicine Lyon-Sud and the Biochemistry department of Hospital Lyon-Sud in the vicinity of the Rhone-Alpes Research Center in Human Nutrition (CRNH-RA). Part of the team is located in IMBL at INSA Lyon.
Main research topics of Team 1
During the last decades, major modifications in our nutritional environment and eating behavior, have largely contributed to the observed overweight, obesity and diabetes epidemics. The main objectives of our research program are 1) to understand at the molecular level the adaptive responses to changes in our nutritional environment and 2) to identify the potential defects in these processes that could contribute to the metabolic pathologies. To this aim, we investigate the adaptive mechanisms to metabolic stress and pollutant exposure under different experimental conditions reflecting as much as possible normal life. Based on the significant advances made over the last years, our strategy rely on 5 complementary and connected research programs:
– “Metabolic adaptation and inflammation of fat tissues during overfeeding” to understand adipose tissue depots remodeling and to propose strategies to fight obesity and prevent its complications;
– «Adipose stem cells in healthy or pathological adipose tissues» to understand the mechanisms initiating adipose tissue alterations and inflammation which lead to the complications of obesity;
– “Metabolic disrupters: impact of environmental pollutants in metabolic diseases” to unravel the contribution and the mechanisms of action of pollutants in triggering or amplifying metabolic diseases;
– “Metabolic adaptations in chronic kidney disease” to define the determinants of metabolic complications, especially insulin resistance, in chronic kidney disease and provide new treatments;
– “Probiotics as a new strategy to fight metabolic diseases” to demonstrate that selected bacterial strains can be powerful agents to treat obese and diabetic patients
Main technical approaches and tools
Nutritional studies in humans in the Research Center for Human Nutrition CRNH-RA. Measurement of insulin sensitivity (hyperinsulinemic euglycemic clamp) / Human tissue resources (muscle and adipose tissue) / Animal models (mice) / Cell culture (stem cells, adipocytes, muscle cells) / Genomics and epigenetics (DNA arrays, RT-qPCR) / Intracellular signaling studies (insulin) / Adipocyte size measurement / Immunocytology / In vitro utilization of adenovirus or shRNA
Topic 1 : Metabolic adaptation and inflammation of fat tissues during ove
rfeeding
Excess calorie intake, exceeding energy expenditure, is one of the characteristics of the modern life and largely contributes to the development of obesity. The mechanisms responsible for the metabolic orientation of energy between storage and catabolism in vivo during overfeeding are not known. In collaboration with the CRNH-RA, we are developing an ambitious research program to characterize these mechanisms usinga overfeeding protocols in humans and in animal models.
In the clinical studies, volunteers (lean and overweight subjects) are submitted to an overfeeding protocol during which they receive about 30% calorie excess each day for several weeks. A detailed analysis of biological, metabolic and anthropometric modifications is performed during the protocol. Several protocols are conducted with different types of supplementation (lipids, fructose or junk food). We are also testing new strategies to prevent the deleterious effects of overfeeding (polyphenols, probiotics). Important results have been already obtained to allow understanding the mechanisms of fuel partitioning in skeletal muscle and the first steps of adipose tissue development when people are gaining weight (Seyssel et al, JCEM, 20145; Alligier et al JCEM, 2012).
Interestingly, some subjects show a preferred orientation of lipid storage in visceral adipose tissue and other ectopic depots such as liver and muscle. This suggests that these subjects probably display a higher risk for the development of metabolic syndrome. We are currently investigating in more details these subjects with the objective of identifying novel risk biomarkers using transcriptomic approach in adipose tissue and skeletal muscle and a metabolomics approach in blood and urine. Parallel to the clinical studies, fat accumulation mechanisms and functions of adipocytes are studied in vitro using human adipocytes in primary culture.
Topic 2 : Adipose stem cells in healthy or pathological adipose tissues
Adipose tissue-derived mesenchymal stem cells (Adipose Stem Cells, ASC), present in large numbers in adipose tissue, not only have the ability to differentiate into adipocytes, but also have many regulatory functions in particular with respect to immune cells. We explore the contribution of these cells to adipose tissue functions and its pathological changes across different lines of research.
One research axis, developed by A. El Jaafari and L. Pirola, is devoted to the understanding of inflammation in adipose tissue. While the well documented presence of macrophages in adipose tissue have been shown to contribute to the low grade inflammation associated with obesity, we have recently involved 2 new players in this process: the adipose-derived mesenchymal stem cells (ASC) and the Th17-lymphocytes (El Jaafari et al, Diabetes, 2015). We have demonstrated that ASC harvested from the adipose tissue of obese individuals (but not from lean donors) can increase IL-17A and IL-1beta secretion by blood mononuclear cells. In turn these cytokines inhibit adipogenesis and reduce insulin action in mature adipocytes. This opens new fields of research to understand the mechanisms of adipose tissue inflammation during weight gain. Because interactions of ASC with Th17 lymphocytes appear to mainly involve cell-cell contact, our goal now is to identify the molecules implicated in these interactions, including the antigens, which might be presented by ASC to Th17 lymphocytes.
Another research project, developed by A. Mey, seeks to understand the origin of the functional differences between the fat depots and their contributions to obesity. She investigates the molecular and biological characteristics of the adipose mesenchymal stem cells (ASC) which contribute to the developmental origin of these depots and remain present in the tissues in adulthood. To understand how the nutritional environment impacts the properties of the ASC at different periodes of life, we have developed the isolation and culture of these cells from different adipose tissue depots in mice and humans.
An interesting property of the ASC is the possibility, as stem cells, to be differentiated in different cell types. We have developed a protocol to generate beta-pancreatic-like cells from human-derived ASC. We will now use these cells to study the impact of ASC-mediated inflammation on beta-cell generation and function in order to better understand the mechanisms leading to beta-cell dysfunction in type-2 diabetes. We also hope to optimize the production of beta-like cells from ASC to propose in the future these cells as therapeutic tools. This will be performed by A. El Jaafari in collaboration with members of team 3 (A-M Madec and C. thivolet) and of the Cell Therapy Unit of Lyon Hospital who recently joined team 1.
Topic 3 : Metabolic disrupters
Apart from genetics, excess calories and lack of physical activity, it is known that environmental pollutants, specifically those endowed with hormonal disrupting activities and acting at low dosage (i.e., the endocrine disruptors), contribute to the epidemic of metabolic disorders. Several epidemiological studies have shown a significant correlation between criteria of the metabolic syndrome and the presence in the blood or urine of pollutants or their metabolites. In addition, experimental studies in rodents, including works from our team (Naville et al, FASEB J, 2013; PLOSOne, 2015; Ruzzin et al, EHP, 2011) established a causal relationship between exposure to chemicals and obesity-related metabolic dysfunctions, such as insulin resistance. Because of the high vulnerability of embryos and newborns, D. Naville and B. Le Magueresse in the team, have developped a model of exposure to very low doses of a cocktail of pollutants (dioxins, PCB153, DEHP and BPA) added to a high-fat high sucrose diet and provide to mice dams and then to their progeny. Changes in biological parameters, fat mass measurement, glucose tolerance and insulin sensitivity tests in the progeny (F1 and after) are studied. Molecular mechanisms are as well investigated both using a candidate-gene approach and a transcriptomic large approach to identify specific genes and pathways leading to the observed metabolic disturbances.
We are also exploring the phenotype of PXR KO mice in collaboration with the group of J. Ruzzin, Bergen University, Norway. Besides, taking into account the crutial role of gut in metabolic health, we make the hypothesis that variations in microbiota may alter the way individuals metabolize and respond to pollutants and we will also test whether interventions on microbiota hold the potential to offer protection from the adverse effects of pollutants.
Topic 4 : Metabolic adptations in chronique kidney disease
Chronic kidney disease (CKD) is frequently associated with peripheral insulin resistance, which is a major cardiovascular risk factor. However, the reasons why CKD patients so often develop insulin resistance, even in absence of overweight or obesity, are largely unknown.
D. Fouque and Ch. Soulage in the team recently demonstrated that the accumulation of uremic toxins, such as p-cresol, in end-stage renal disease could be a key factor for the development of insulin resistance (Koppe et al. Amer Soc Nephrol, 2013). Using mouse model of CKD, we are currently extend this concept to other uremic toxins, like endoxyl sulfate, and try to define their mechanisms of action, focusing on the activation of nuclear receptors, such as arylhydrocarbon receptor (AhR, i.e. the nuclear receptor of dioxins). The mechanisms underlying the development of insulin resistance will be investigated in vitro using adipocytes and muscle cells in culture incubated with uremic toxins. Identifications of the pathways mediating the deleterious effects of these compounds and the potential role of AhR will be explored in details in these in vitro systems. We will then further explore the relevance of the findings in our cohort of patients with CKD. The role of the intestinal flora will also be investigated with the aim of elaborating pro/pre-biotics strategies to modulate the production of uremic toxins.
Other research projects include the study of the impact of peritoneal dialysis on intra-abdominal white adipose tissue functions using an original mouse model of peritoneal dialysis under development in the laboratory. The relevance of this pre-clinical model will be assessed in subcutaneous and omental adipose tissue biopsies from patients treated by peritoneal dialysis in which we will analyse fat cell size, histology (immune cell infiltration, fibrosis), adipocyte functions and adipokine secretion in relation to glucose exposure, peritoneal transport type and metabolic risk factors.
Topic 5 : Probiotics as a new stategy to fight metabolic diseases
The use of probiotics with the aim of modulating blood glucose and hence improving diabetes has been envisaged for a long time, particularly as nutritional supplements, but the discovery of the critical role of gut microbiota in metabolic diseases has logically boosted research efforts in this field. Obesity and type 2 diabetes are indeed associated with perturbation of the composition and function of the gut microbiota (called dysbiosis), globally characterized by change in the ratio between Firmicutes (Gram-positive) and Bacteroidetes (Gram-negative), the two major phyla in the gut. Furthermore, it has been recently demonstrated that the gut microbiota certainly plays a critical role in the pathogenesis of these diseases. Several bacterial strains, used as probiotics, have recently shown clear beneficial actions on glucose tolerance and insulin sensitivity in mouse models. However, the effects are less important in humans and their mechanisms of action only partly defined. Our goal is therefore to identify potent bacterial strains with strong beneficial effects for human health and to propose them as new probiotics for metabolic diseases prevention and/or treatment.
To identify these new strains, we are working in close collaboration with the IGFL team of F. Leulier (a leader in the field of host-bacteria interactions in drosophila) (mettre le lien: http://igfl.ens-lyon.fr/equipes/f.-leulier-functional-genomics-of-host-intestinal-bacteria-interactions) who has developed an innovative screening system to qualify Lactobacillus strains with anti-diabetic properties (under patenting).
We recently used together a variant of this powerful screening system for functional strain qualification to demonstrate for the first time the critical role of microbiota and of a selected L.plantarum strain in the juvenile growth (Schwarzer et al. Science 2016). We are currently qualifying relevant strains for their anti-diabetic properties in diabetic mice, as a pre-clinical test before their evaluation in patients. In parallel, as indicated in the Topics 2 and 3 before, bacterial strains with probiotic properties are also evaluated for their potential to buffer the toxic effects of a cocktail of pollutants in exposed mice and to control the production of uremic toxins in a model of mouse with chronic kidney disease.
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Team 1 Leaders | |||
VIDAL | Hubert | DR1 | hubert.vidal@univ-lyon1.fr |
LAVILLE | Martine | DR1 | martine.laville@univ-lyon1.fr |
Members |
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BENOIT | Julien | PhD | benoit.julien@univ-lyon1.fr |
BERGER-DANTY | Emmanuelle | CR1 | emmanuelle.danty@univ-lyon1.fr |
CHARRIE | Anne | MCUPH | anne.charrie@univ-lyon1.fr |
DA SILVA | Joao Henriq | Postdoctorant | joaohenriq@hotmail.com |
DISSE | Emmanuel | PUPH | emmanuel.disse@chu-lyon.fr |
DRAI | Jocelyne | PH | jocelyne.drai@chu-lyon.fr |
DURAND | Christine | TR | christine2.durand@inserm.fr |
ELJAAFARI | Assia | PH | assia.eljaafari@univ-lyon1.fr |
FALANDRY | Claire | PUPH | claire.falandry@chu-lyon.fr |
FOUQUE | Denis | PUPH | denis.fouque@chu-lyon.fr |
GELOEN | Alain | DR2 | alain.geloen@insa-lyon.fr |
GERARD | Céline | Postdoctorante | celine.gerard@inserm.fr |
GOUDABLE | Joëlle | PUPH | joelle.goudable@univ-lyon1.fr |
HOIBIAN | Elsa | PhD | elsa.hoibian@insa-lyon.fr |
JOBEILI | Lara | PhD | lara.jobeili@gmail.com |
JULIEN | Benoit | PhD | benoit.julien@univ-lyon1.fr |
KAISERLIAN | Dominique | DR1 | dominique.kaiserlian@inserm.fr |
LE MAGUERESSE | Brigitte | DR2 | brigitte.lemagueresse@inserm.fr |
LEFEVRE | Camille | PhD | camille.lefevre@etu.univ-lyon1.fr |
MEUGNIER | Emmanuelle | IR | emmanuelle.meugnier@univ-lyon1.fr |
MEY | Anne | CR1 | anne.mey@inra.fr |
MOJALLAL | Alain-Ali | PUPH | dr.mojallal@gmail.com |
NATAF | Serge | PUPH | serge.nataf@chu-lyon.fr |
NAVILLE | Danielle | CR1 | danielle.naville@inserm.fr |
NAZARE | Julie-Anne | MCU | julie-anne.nazare@univ-lyon1.fr |
PAYS | Laurent | MCU | laurent.pays@univ-lyon1.fr |
PELLETIER | Caroline | PhD | c.pelletier.5@gmail.com |
PINTEUR | Claudie | TR | claudie.pinteur@inserm.fr |
PIROLA | Luciano | CR1 | luciano.pirola@univ-lyon1.fr |
PUGEAT | Michel | PUPH émérite | michel.pugeat@chu-lyon.fr |
SEGRESTIN | Bérénice | PhD | berenice.segrestin@gmail.com |
SOULAGE | Christophe | MCU | christophe.soulage@insa-lyon.fr |
VEGA | Nathalie | TR | nathalie.vega@univ-lyon1.fr |
2020 (january-june)
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- Alvarenga, L., R. Salarolli, L. Cardozo, R. S. Santos, J. S. de Brito, J. A. Kemp, D. Reis, B. R. de Paiva, P. Stenvinkel, B. Lindholm, D. Fouque and D. Mafra (2020) Impact of curcumin supplementation on expression of inflammatory transcription factors in hemodialysis patients: A pilot randomized, double-blind, controlled study Clin Nutr 10.1016/j.clnu.2020.03.007
- Aparicio, T., A. Darut-Jouve, F. Khemissa Akouz, C. Montérymard, P. Artru, L. Cany, O. Romano, B. Valenza, C. Le Foll, C. Delbaldo, C. Falandry, E. Norguet Monnereau, M. Ben Abdelghani, D. Smith, Y. Rinaldi, D. Père Verge, N. Baize, E. Maillard, A. Dohan, G. Des Guetz, F. Pamoukdjian and C. Lepage (2020) Single-arm phase II trial to evaluate efficacy and tolerance of regorafenib monotherapy in patients over 70 with previously treated metastatic colorectal adenocarcinoma FFCD 1404 – REGOLD J Geriatr Oncol 10.1016/j.jgo.2020.04.001
- Bouchet, M., A. Lainé, C. Boyault, M. Proponnet-Guerault, E. Meugnier, L. Bouazza, C. W. S. Kan, S. Geraci, S. El-Moghrabi, H. Hernandez-Vargas, C. Benetollo, Y. Yoshiko, M. Duterque-Coquillaud, P. Clézardin, J. C. Marie and E. Bonnelye (2020) ERRα Expression in Bone Metastases Leads to an Exacerbated Antitumor Immune Response Cancer Res 80 13 2914-2926 10.1158/0008-5472.Can-19-3584
- Cariou, B., S. Hadjadj, M. Wargny, M. Pichelin, A. Al-Salameh, I. Allix, C. Amadou, G. Arnault, F. Baudoux, B. Bauduceau, S. Borot, M. Bourgeon-Ghittori, O. Bourron, D. Boutoille, F. Cazenave-Roblot, C. Chaumeil, E. Cosson, S. Coudol, P. Darmon, E. Disse, A. Ducet-Boiffard, B. Gaborit, M. Joubert, V. Kerlan, B. Laviolle, L. Marchand, L. Meyer, L. Potier, G. Prevost, J. P. Riveline, R. Robert, P. J. Saulnier, A. Sultan, J. F. Thébaut, C. Thivolet, B. Tramunt, C. Vatier, R. Roussel, J. F. Gautier and P. Gourdy (2020) Phenotypic characteristics and prognosis of inpatients with COVID-19 and diabetes: the CORONADO study Diabetologia 63 8 1500-1515 10.1007/s00125-020-05180-x
- Carrero, J. J., A. González-Ortiz, C. M. Avesani, S. J. L. Bakker, V. Bellizzi, P. Chauveau, C. M. Clase, A. Cupisti, A. Espinosa-Cuevas, P. Molina, K. Moreau, G. B. Piccoli, A. Post, S. Sezer and D. Fouque (2020) Plant-based diets to manage the risks and complications of chronic kidney disease Nat Rev Nephrol 10.1038/s41581-020-0297-2
- Caussy, C., F. Pattou, F. Wallet, C. Simon, S. Chalopin, C. Telliam, D. Mathieu, F. Subtil, E. Frobert, M. Alligier, D. Delaunay, P. Vanhems, M. Laville, M. Jourdain and E. Disse (2020) Prevalence of obesity among adult inpatients with COVID-19 in France Lancet Diabetes Endocrinol 8 7 562-564 10.1016/s2213-8587(20)30160-1
- Caussy, C., F. Wallet, M. Laville and E. Disse (2020) Obesity is Associated with Severe Forms of COVID-19 Obesity (Silver Spring) 28 7 1175 10.1002/oby.22842
- Ciesielski, O., M. Biesiekierska, B. Panthu, V. Vialichka, L. Pirola and A. Balcerczyk (2020) The Epigenetic Profile of Tumor Endothelial Cells. Effects of Combined Therapy with Antiangiogenic and Epigenetic Drugs on Cancer Progression Int J Mol Sci 21 7 10.3390/ijms21072606
- Clément, K., M. Coupaye, M. Laville, J. M. Oppert and O. Ziegler (2020) COVID-19: a lever for the recognition of obesity as a disease? The French experience Obesity (Silver Spring) 10.1002/oby.22924
- Cugnet Anceau, C., J. Abeillon, D. Maillet, F. Borson-Chazot and E. Disse (2020) [Thyroid dysfunctions secondary to cancer immunotherapy] Bull Cancer 107 2 262-271 10.1016/j.bulcan.2019.10.005
- Dąbek, A., M. Wojtala, L. Pirola and A. Balcerczyk (2020) Modulation of Cellular Biochemistry, Epigenetics and Metabolomics by Ketone Bodies. Implications of the Ketogenic Diet in the Physiology of the Organism and Pathological States Nutrients 12 3 10.3390/nu12030788
- de Oliveira Lira, A., J. L. de Brito Alves, M. Pinheiro Fernandes, D. Vasconcelos, D. F. Santana, J. H. da Costa-Silva, B. Morio, C. Góis Leandro and L. Pirola (2020) Maternal low protein diet induces persistent expression changes in metabolic genes in male rats World J Diabetes 11 5 182-192 10.4239/wjd.v11.i5.182
- du Payrat, J. A., C. Cugnet-Anceau, D. Maillet, M. Levy, G. Raverot, E. Disse and F. Borson-Chazot (2020) [Checkpoint inhibitors-induced hypophysitis] Bull Cancer 107 4 490-498 10.1016/j.bulcan.2020.01.012
- Espi, M., L. Koppe, D. Fouque and O. Thaunat (2020) Chronic Kidney Disease-Associated Immune Dysfunctions: Impact of Protein-Bound Uremic Retention Solutes on Immune Cells Toxins (Basel) 12 5 10.3390/toxins12050300
- Facchinetti, F., M. Appetecchia, C. Aragona, A. Bevilacqua, M. S. Bezerra Espinola, M. Bizzarri, R. D’Anna, D. Dewailly, E. Diamanti-Kandarakis, I. Hernández Marín, Z. A. Kamenov, E. Kandaraki, A. S. Laganà, G. Monastra, M. Montanino Oliva, J. E. Nestler, F. Orio, A. C. Ozay, O. Papalou, L. Pkhaladze, G. Porcaro, N. Prapas, C. O. Soulage, A. Stringaro, A. Wdowiak and V. Unfer (2020) Experts’ opinion on inositols in treating polycystic ovary syndrome and non-insulin dependent diabetes mellitus: a further help for human reproduction and beyond Expert Opin Drug Metab Toxicol 16 3 255-274 10.1080/17425255.2020.1737675
- Facchinetti, F., V. Unfer, D. Dewailly, Z. A. Kamenov, E. Diamanti-Kandarakis, A. S. Laganà, J. E. Nestler and C. O. Soulage (2020) Inositols in Polycystic Ovary Syndrome: An Overview on the Advances Trends Endocrinol Metab 31 6 435-447 10.1016/j.tem.2020.02.002
- Falandry, C., C. Filteau, C. Ravot and O. Le Saux (2020) Challenges with the management of older patients with cancer during the COVID-19 pandemic J Geriatr Oncol 11 5 747-749 10.1016/j.jgo.2020.03.020
- Florens, N., C. Calzada, S. Lemoine, M. M. Boulet, N. Guillot, C. Barba, J. Roux, F. Delolme, A. Page, J. M. Poux, M. Laville, P. Moulin, L. Soulère, F. Guebre-Egziabher, L. Juillard and C. O. Soulage (2020) CKD Increases Carbonylation of HDL and Is Associated with Impaired Antiaggregant Properties J Am Soc Nephrol 31 7 1462-1477 10.1681/asn.2019111205
- Fragoso, J., G. Carvalho Jurema Santos, H. Thomaz da Silva, V. Oliveira Nogueira, E. Loizon, H. Vidal, J. H. Costa-Silva, R. da Silva Aragão, L. Pirola and C. G. Leandro (2020) Maternal physical activity-induced adaptive transcriptional response in brain and placenta of mothers and rat offspring J Dev Orig Health Dis 11 2 108-117 10.1017/s2040174419000333
- Gross-Amat, O., M. Guillen, J. P. Gimeno, M. Salzet, N. Lebonvallet, L. Misery, C. Auxenfans and S. Nataf (2020) Molecular Mapping of Hydrogen Sulfide Targets in Normal Human Keratinocytes Int J Mol Sci 21 13 10.3390/ijms21134648
- Hachem, M., H. Nacir, M. Picq, M. Belkouch, N. Bernoud-Hubac, A. Windust, L. Meiller, V. Sauvinet, N. Feugier, S. Lambert-Porcheron, M. Laville and M. Lagarde (2020) Docosahexaenoic Acid (DHA) Bioavailability in Humans after Oral Intake of DHA-Containing Triacylglycerol or the Structured Phospholipid AceDoPC((R)) Nutrients 12 1 10.3390/nu12010251
- Heerspink, H. J. L., D. Fouque and C. Wanner (2020) Editorial: The role of sodium-glucose cotransporter 2 inhibitors in the management of chronic kidney disease Nephrol Dial Transplant 35 Suppl 1 i1-i2 10.1093/ndt/gfz282
- Iceta, S., J. Benoit, P. Cristini, S. Lambert-Porcheron, B. Segrestin, M. Laville, E. Poulet and E. Disse (2020) Attentional bias and response inhibition in severe obesity with food disinhibition: a study of P300 and N200 event-related potential Int J Obes (Lond) 44 1 204-212 10.1038/s41366-019-0360-x
- Kalantar-Zadeh, K., H. M. Kramer and D. Fouque (2020) High-protein diet is bad for kidney health: unleashing the taboo Nephrol Dial Transplant 35 1 1-4 10.1093/ndt/gfz216
- Koppe, L. and C. O. Soulage (2020) Preservation of residual kidney function to reduce non-urea solutes toxicity in haemodialysis Nephrol Dial Transplant 35 5 733-736 10.1093/ndt/gfz224
- Laugerette, F., C. Vors, M. Alligier, G. Pineau, J. Drai, C. Knibbe, B. Morio, S. Lambert-Porcheron, M. Laville, H. Vidal and M. C. Michalski (2020) Postprandial Endotoxin Transporters LBP and sCD14 Differ in Obese vs. Overweight and Normal Weight Men during Fat-Rich Meal Digestion Nutrients 12 6 10.3390/nu12061820
- Laville, S. M., V. Gras-Champel, J. Moragny, M. Metzger, C. Jacquelinet, C. Combe, D. Fouque, M. Laville, L. Frimat, B. M. Robinson, B. Stengel, Z. A. Massy and S. Liabeuf (2020) Adverse Drug Reactions in Patients with CKD Clin J Am Soc Nephrol 10.2215/cjn.01030120
- Legrand, K., E. Speyer, B. Stengel, L. Frimat, W. Ngueyon Sime, Z. A. Massy, D. Fouque, M. Laville, C. Combe, C. Jacquelinet, A. C. Durand, S. Edet, S. Gentile, S. Briançon and C. Ayav (2020) Perceived Health and Quality of Life in Patients With CKD, Including Those With Kidney Failure: Findings From National Surveys in France Am J Kidney Dis 75 6 868-878 10.1053/j.ajkd.2019.08.026
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- Monteiro, E. B., E. D. R. Soares, P. L. Trindade, G. F. de Bem, A. C. Resende, M. Passos, C. O. Soulage and J. B. Daleprane (2020) Uraemic toxin-induced inflammation and oxidative stress in human endothelial cells: protective effect of polyphenol-rich extract from açaí Exp Physiol 105 3 542-551 10.1113/ep088080
- Mourey, L., C. Falandry, L. de Decker, R. Boulahssass, E. Carola, L. Bengrine Lefevre, T. Cudennec, E. Brain, E. Paillaud and P. Soubeyran (2020) Taking care of older patients with cancer in the context of COVID-19 pandemic Lancet Oncol 21 5 e236 10.1016/s1470-2045(20)30229-1
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- Vinoy, S., Laville, M. and Feskens, E. J. (2016) Slow-release carbohydrates: growing evidence on metabolic responses and public health interest. Summary of the symposium held at the 12th European Nutrition Conference (FENS 2015) Food Nutrition Research 60 31662
- Vouillarmet, J. and Laville, M. (2016) A Case of Familial Partial Lipodystrophy: From Clinical Phenotype to Genetics Canadian Journal of Diabetes 40 376-37
- Wojtala, M., Pirola, L. and Balcerczyk, A. (2016) Modulation of the vascular endothelium functioning by dietary components, the role of epigenetics Biofactors doi: 10.1002/biof.1306
2015
1. Bastard, J. P., Rabasa-Lhoret, R., Laville, M., and Disse, E. (2015) Surrogate measures of insulin sensitivity vs the hyperinsulinaemic-euglycaemic clamp: a meta-analysis. Are there not some surrogate indexes lost in this story? Diabetologia. 58, 414-415
2. Benoit, B., Laugerette, F., Plaisancie, P., Geloen, A., Bodennec, J., Estienne, M., Pineau, G., Bernalier-Donadille, A., Vidal, H., and Michalski, M. C. (2015) Increasing fat content from 20 to 45 wt% in a complex diet induces lower endotoxemia in parallel with an increased number of intestinal goblet cells in mice. Nutrition Research. 35, 346-356
3. Berger, E., Heraud, S., Mojallal, A., Lequeux, C., Weiss-Gayet, M., Damour, O., and Geloen, A. (2015) Pathways commonly dysregulated in mouse and human obese adipose tissue: FAT/CD36 modulates differentiation and lipogenesis. Adipocyte. 4, 161-180
4. Berger, E., Vega, N., Weiss-Gayet, M., and Geloen, A. (2015) Gene Network Analysis of Glucose Linked Signaling Pathways and Their Role in Human Hepatocellular Carcinoma Cell Growth and Survival in HuH7 and HepG2 Cell Lines. BioMed Research International. 2015, 821761
5. Betry, C., Challan-Belval, M. A., Bernard, A., Charrie, A., Drai, J., Laville, M., Thivolet, C., and Disse, E. (2015) Increased TSH in obesity: Evidence for a BMI-independent association with leptin. Diabetes & Metabolism. 41, 248-251
6. Blond, E., Goudable, J., and Laville, M. (2015) Nonalcoholic Fatty liver disease and hyperuricemia: a close relation with hepatic insulin resistance after nicotinic Acid treatment? Hormone and Metabolic Research. 47, 546-547
7. Boschetti, G., Garnero, P., Moussata, D., Cuerq, C., Preaudat, C., Duclaux-Loras, R., Mialon, A., Drai, J., Flourie, B., and Nancey, S. (2015) Accuracies of serum and fecal S100 proteins (calprotectin and calgranulin C) to predict the response to TNF antagonists in patients with Crohn’s disease. Inflammatory Bowel Diseases. 21, 331-336
8. Boschetti, G., Laidet, M., Moussata, D., Stefanescu, C., Roblin, X., Phelip, G., Cotte, E., Passot, G., Francois, Y., Drai, J., Del Tedesco, E., Bouhnik, Y., Flourie, B., and Nancey, S. (2015) Levels of Fecal Calprotectin Are Associated With the Severity of Postoperative Endoscopic Recurrence in Asymptomatic Patients With Crohn’s Disease. The American Journal of Gastroenterology. 110, 865-872
9. Capel, F., Acquaviva, C., Pitois, E., Laillet, B., Rigaudiere, J. P., Jouve, C., Pouyet, C., Gladine, C., Comte, B., Vianey Saban, C., and Morio, B. (2015) DHA at nutritional doses restores insulin sensitivity in skeletal muscle by preventing lipotoxicity and inflammation. The Journal of Nutritional Biochemistry. 26, 949-959
10. Chevalier, N., Brucker-Davis, F., Lahlou, N., Coquillard, P., Pugeat, M., Pacini, P., Panaia-Ferrari, P., Wagner-Mahler, K., and Fenichel, P. (2015) A negative correlation between insulin-like peptide 3 and bisphenol A in human cord blood suggests an effect of endocrine disruptors on testicular descent during fetal development. Human Reproduction. 30, 447-453
11. Chriett, S., and Pirola, L. (2015) Essential roles of four-carbon backbone chemicals in the control of metabolism. World Journal of Biological Chemistry. 6, 223-230
12. Croze, M. L., Geloen, A., and Soulage, C. O. (2015) Abnormalities in myo-inositol metabolism associated with type 2 diabetes in mice fed a high-fat diet: benefits of a dietary myo-inositol supplementation. The British Journal of Nutrition. 113, 1862-1875
13. Cuerq, C., Peretti, N., Chikh, K., Mialon, A., Guillaumont, M., Drai, J., and Blond, E. (2015) Overview of the in vitro stability of commonly measured vitamins and carotenoids in whole blood. Annals of Clinical Biochemistry. 52, 259-269
14. Eljaafari, A., Robert, M., Chehimi, M., Chanon, S., Durand, C., Vial, G., Bendridi, N., Madec, A. M., Disse, E., Laville, M., Rieusset, J., Lefai, E., Vidal, H., and Pirola, L. (2015) Adipose Tissue-Derived Stem Cells From Obese Subjects Contribute to Inflammation and Reduced Insulin Response in Adipocytes Through Differential Regulation of the Th1/Th17 Balance and Monocyte Activation. Diabetes. 64, 2477-2488
15. Hachem, M., Geloen, A., Van, A. L., Foumaux, B., Fenart, L., Gosselet, F., Da Silva, P., Breton, G., Lagarde, M., Picq, M., and Bernoud-Hubac, N. (2015) Efficient Docosahexaenoic Acid Uptake by the Brain from a Structured Phospholipid. Molecular neurobiology.
16. Heinrich-Balard, L., Zeinyeh, W., Dechaud, H., Rivory, P., Roux, A., Pugeat, M., and Cohen, R. (2015) Inverse relationship between hSHBG affinity for testosterone and hSHBG concentration revealed by surface plasmon resonance. Molecular and cellular endocrinology. 399, 201-207
17. Honnorat, D., Disse, E., Millot, L., Mathiotte, E., Claret, M., Charrie, A., Drai, J., Garnier, L., Maurice, C., Durand, E., Simon, C., Dupuis, O., and Thivolet, C. (2015) Are third-trimester adipokines associated with higher metabolic risk among women with gestational diabetes? Diabetes & Metabolism. 41, 393-400
18. Huvenne, H., Le Beyec, J., Pepin, D., Alili, R., Kherchiche, P. P., Jeannic, E., Frelut, M. L., Lacorte, J. M., Nicolino, M., Viard, A., Laville, M., Ledoux, S., Tounian, P., Poitou, C., Dubern, B., and Clement, K. (2015) Seven novel deleterious LEPR mutations found in early-onset obesity: a DeltaExon6-8 shared by subjects from Reunion Island, France, suggests a founder effect. The Journal of Clinical Endocrinology and Metabolism. 100, E757-766
19. Koppe, L., Mafra, D., and Fouque, D. (2015) Probiotics and chronic kidney disease. Kidney international. 88, 958-966
20. Le Guen, M., Chate, V., Hininger-Favier, I., Laillet, B., Morio, B., Pieroni, G., Schlattner, U., Pison, C., and Dubouchaud, H. (2016) A 9-wk docosahexaenoic acid-enriched supplementation improves endurance exercise capacity and skeletal muscle mitochondrial function in adult rats. Am J Physiol Endocrinol Metab. 310, E213-224
21. Lecomte, M., Couedelo, L., Meugnier, E., Plaisancie, P., Letisse, M., Benoit, B., Gabert, L., Penhoat, A., Durand, A., Pineau, G., Joffre, F., Geloen, A., Vaysse, C., Laugerette, F., and Michalski, M. C. (2016) Dietary emulsifiers from milk and soybean differently impact adiposity and inflammation in association with modulation of colonic goblet cells in high-fat fed mice. Molecular nutrition & food research. 60, 609-620
22. Mafra, D., and Fouque, D. (2015) Gut microbiota and inflammation in chronic kidney disease patients. Clin Kidney J. 8, 332-334
23. Millon, A., Sigovan, M., Boussel, L., Mathevet, J. L., Louzier, V., Paquet, C., Geloen, A., Provost, N., Majd, Z., Patsouris, D., Serusclat, A., and Canet-Soulas, E. (2015) Low WSS Induces Intimal Thickening, while Large WSS Variation and Inflammation Induce Medial Thinning, in an Animal Model of Atherosclerosis. PLoS One. 10, e0141880
24. Naville, D., Labaronne, E., Vega, N., Pinteur, C., Canet-Soulas, E., Vidal, H., and Le Magueresse-Battistoni, B. (2015) Metabolic outcome of female mice exposed to a mixture of low-dose pollutants in a diet-induced obesity model. PLoS One. 10, e0124015
25. Papastathi, C., Disse, E., Berthiller, J., Laville, M., Gouillat, C., and Robert, M. (2015) Impact of Pregnancy on Weight Loss and Quality of Life Following Gastric Banding. Obesity surgery.
26. Perez, E. C., Elie, J. E., Boucaud, I. C., Crouchet, T., Soulage, C. O., Soula, H. A., Theunissen, F. E., and Vignal, C. (2015) Physiological resonance between mates through calls as possible evidence of empathic processes in songbirds. Hormones and Behavior. 75, 130-141
27. Perrin, L., Loizides-Mangold, U., Skarupelova, S., Pulimeno, P., Chanon, S., Robert, M., Bouzakri, K., Modoux, C., Roux-Lombard, P., Vidal, H., Lefai, E., and Dibner, C. (2015) Human skeletal myotubes display a cell-autonomous circadian clock implicated in basal myokine secretion. Molecular metabolism. 4, 834-845
28. Revel, F., Gilbert, T., Roche, S., Drai, J., Blond, E., Ecochard, R., and Bonnefoy, M. (2015) Influence of oxidative stress biomarkers on cognitive decline. Journal of Alzheimer’s disease. 45, 553-560
29. Rieusset, J., Fauconnier, J., Paillard, M., Belaidi, E., Tubbs, E., Chauvin, M. A., Durand, A., Bravard, A., Teixeira, G., Bartosch, B., Michelet, M., Theurey, P., Vial, G., Demion, M., Blond, E., Zoulim, F., Gomez, L., Vidal, H., Lacampagne, A., and Ovize, M. (2016) Disruption of calcium transfer from ER to mitochondria links alterations of mitochondria-associated ER membrane integrity to hepatic insulin resistance. Diabetologia. 59, 614-623
30. Robert, M., Pechoux, A., Marion, D., Laville, M., Gouillat, C., and Disse, E. (2015) Relevance of Roux-en-Y gastric bypass volumetry using 3-dimensional gastric computed tomography with gas to predict weight loss at 1 year. Surgery for obesity and related diseases. 11, 26-31
31. Rossignol, P., Massy, Z. A., Azizi, M., Bakris, G., Ritz, E., Covic, A., Goldsmith, D., Heine, G. H., Jager, K. J., Kanbay, M., Mallamaci, F., Ortiz, A., Vanholder, R., Wiecek, A., Zoccali, C., London, G. M., Stengel, B., Fouque, D., group, Era-Edta Eureca- m working, Red de Investigacion Renal, network, Cardiovascular, and Renal Clinical Trialists, network (2015) The double challenge of resistant hypertension and chronic kidney disease. Lancet. 386, 1588-1598
32. Salvatore, G., Bernoud-Hubac, N., Bissay, N., Debard, C., Daira, P., Meugnier, E., Proamer, F., Hanau, D., Vidal, H., Arico, M., Delprat, C., and Mahtouk, K. (2015) Human monocyte-derived dendritic cells turn into foamy dendritic cells with IL-17A. Journal of lipid research. 56, 1110-1122
33. Soula, H. A., Geloen, A., and Soulage, C. O. (2015) Model of adipose tissue cellularity dynamics during food restriction. Journal of theoretical biology. 364, 189-196
34. Steiber, A. L., Leon, J. B., Hand, R. K., Murphy, W. J., Fouque, D., Parrott, J. S., Kalantar-Zadeh, K., and Cuppari, L. (2015) Using a web-based nutrition algorithm in hemodialysis patients. Journal of renal nutrition. 25, 6-16
35. Vella, R. E., Pillon, N. J., Zarrouki, B., Croze, M. L., Koppe, L., Guichardant, M., Pesenti, S., Chauvin, M. A., Rieusset, J., Geloen, A., and Soulage, C. O. (2015) Ozone exposure triggers insulin resistance through muscle c-Jun N-terminal kinase activation. Diabetes. 64, 1011-1024
36. Vericel, E., Colas, R., Calzada, C., Le, Q. H., Feugier, N., Cugnet, C., Vidal, H., Laville, M., Moulin, P., and Lagarde, M. (2015) Moderate oral supplementation with docosahexaenoic acid improves platelet function and oxidative stress in type 2 diabetic patients. Thrombosis and haemostasis. 114, 289-296
37. Vial, G., Chauvin, M. A., Bendridi, N., Durand, A., Meugnier, E., Madec, A. M., Bernoud-Hubac, N., Pais de Barros, J. P., Fontaine, E., Acquaviva, C., Hallakou-Bozec, S., Bolze, S., Vidal, H., and Rieusset, J. (2015) Imeglimin normalizes glucose tolerance and insulin sensitivity and improves mitochondrial function in liver of a high-fat, high-sucrose diet mice model. Diabetes. 64, 2254-2264
38. Villain, C., Ecochard, R., Genet, L., Jean, G., Kuentz, F., Lataillade, D., Legrand, E., Moreau-Gaudry, X., and Fouque, D. (2015) Impact of BMI Variations on Survival in Elderly Hemodialysis Patients. Journal of renal nutrition. 25, 488-493
39. Vogelzang, J. L., van Stralen, K. J., Noordzij, M., Diez, J. A., Carrero, J. J., Couchoud, C., Dekker, F. W., Finne, P., Fouque, D., Heaf, J. G., Hoitsma, A., Leivestad, T., de Meester, J., Metcalfe, W., Palsson, R., Postorino, M., Ravani, P., Vanholder, R., Wallner, M., Wanner, C., Groothoff, J. W., and Jager, K. J. (2015) Mortality from infections and malignancies in patients treated with renal replacement therapy: data from the ERA-EDTA registry. Nephrology, dialysis, transplantation. 30, 1028-1037
40. Vors, C., Drai, J., Gabert, L., Pineau, G., Laville, M., Vidal, H., Guichard, E., Michalski, M. C., and Feron, G. (2015) Salivary composition in obese vs normal-weight subjects: towards a role in postprandial lipid metabolism? International Journal of Obesity. 39, 1425-1428
41. Vors, C., Pineau, G., Drai, J., Meugnier, E., Pesenti, S., Laville, M., Laugerette, F., Malpuech-Brugere, C., Vidal, H., and Michalski, M. C. (2015) Postprandial Endotoxemia Linked With Chylomicrons and Lipopolysaccharides Handling in Obese Versus Lean Men: A Lipid Dose-Effect Trial. The Journal of Clinical Endocrinology and Metabolism. 100, 3427-3435