Changes in Microbiota and Bacterial Protein Caseinolytic Peptidase B During Food Restriction in Mice: Relevance for the Onset and Perpetuation of Anorexia Nervosa.
Manon DominiqueRomain LegrandMarie GalmicheSaïda AzharCamille DeroissartCharlène GuérinJean-Luc do RegoFatima LeonSéverine NobisGrégory LambertNicolas LucasPierre DéchelottePublished in: Nutrients (2019)
Microbiota contributes to the regulation of eating behavior and might be implicated in the pathophysiology of anorexia nervosa. ClpB (Caseinolytic peptidase B) protein produced mainly by the Enterobacteriaceae family has been identified as a conformational mimetic of α-MSH, which could result in similar anorexigenic effects. The aim of this study was to highlight the role of the microbiome and the ClpB protein in deregulation and self-maintenance of anorexia pathology. Male C57Bl/6 mice were undergone to the ABA (Activity-Based Anorexia) protocol: after 5 days of acclimatization, both ABA and LFA (Limited Food Access) mice had progressively limited access to food until D17. At the end of protocol, the plasma ClpB concentration and Enterobacteriaceae DNA in colonic content were measured. As expected, dietary restriction induced lost weight in LFA and ABA mice. At D10, colonic permeability and plasma concentration of the ClpB protein were significantly increased in LFA and ABA mice vs. controls. At D17, plasma concentration of ClpB was increased in LFA and ABA mice and, it was correlated with proportion of Enterobacteriaceae in the faeces. These abnormally high ClpB concentrations and all associated factors, and therefore might contribute to the initiation and/or perpetuation of anorexia nervosa by interfering with satiety signaling.
Keyphrases
- anorexia nervosa
- high fat diet induced
- transcription factor
- pseudomonas aeruginosa
- multidrug resistant
- randomized controlled trial
- physical activity
- protein protein
- weight loss
- metabolic syndrome
- wild type
- insulin resistance
- molecular dynamics
- single molecule
- risk assessment
- oxidative stress
- molecular dynamics simulations
- circulating tumor cells