Sex-related effects of nutritional supplementation of Escherichia coli: relevance to eating disorders

Nutrition. 2015 Mar;31(3):498-507. doi: 10.1016/j.nut.2014.11.003. Epub 2014 Dec 5.

Abstract

Objectives: The biological background of sex-related differences in the development of eating disorders (EDs) is unknown. Recent data showed that gut bacteria Escherichia coli induce autoantibodies against anorexigenic α-melanocyte-stimulating hormone (α-MSH) associated with psychopathology in ED. The aim of this study was to compare the effects of E. coli on feeding and autoantibodies against α-MSH and adrenocorticotropic hormone (ACTH), between female and male rats.

Methods: Commensal E. coli K12 were given in a culture medium daily to adult Wistar rats by intragastric gavage over a 3-wk period; control rats received culture medium only.

Results: Before gavage, E. coli K12 DNA was detected in feces of female but not male rats. E. coli provision was accompanied by an increase in body weight gain in females, but a decrease in body weight gain and food intake in males. Independent of E. coli treatment, plasma levels of anti-α-MSH and ACTH immunoglobulin (Ig)G were higher in female than male rats. Females responded to E. coli by increasing α-MSH IgG levels and affinity, but males by increasing α-MSH IgM levels. Affinity of IgG for ACTH was increased in both E. coli-treated females and males, although with different kinetics. IgG from females stimulated more efficiently α-MSH-induced cyclic adenosine monophosphate production by melanocortin 4 receptor-expressing cells compared with IgG from males.

Discussion: Sex-related response to how E. coli affects feeding and anti-melanocortin hormone antibody production may depend on the presence of these bacteria in the gut before E. coli supplementation. These data suggest that sex-related presence of certain gut bacteria may represent a risk factor for ED development.

Keywords: Animal models; Anorexia nervosa; Anxiety; Body weight; Bulimia; Eating disorders; Feeding; Microbiota; Neuropeptides.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Monophosphate / metabolism
  • Adrenocorticotropic Hormone / immunology
  • Animals
  • Autoantibodies / blood*
  • Colon / microbiology*
  • Dietary Supplements
  • Eating / immunology*
  • Escherichia coli*
  • Feces / microbiology
  • Feeding and Eating Disorders / immunology
  • Feeding and Eating Disorders / microbiology*
  • Female
  • Gastrointestinal Microbiome / immunology*
  • Immunoglobulin G / blood
  • Immunoglobulin M / blood
  • Male
  • Melanocortins / immunology*
  • Probiotics
  • Rats, Wistar
  • Receptor, Melanocortin, Type 4 / metabolism
  • Sex Factors
  • Weight Gain
  • alpha-MSH / immunology

Substances

  • Autoantibodies
  • Immunoglobulin G
  • Immunoglobulin M
  • Melanocortins
  • Receptor, Melanocortin, Type 4
  • Adenosine Monophosphate
  • alpha-MSH
  • Adrenocorticotropic Hormone