Maternal deprivation affects the neuromuscular protein profile of the rat colon in response to an acute stressor later in life

J Proteomics. 2008 Apr 30;71(1):80-8. doi: 10.1016/j.jprot.2008.01.007. Epub 2008 Jan 18.

Abstract

Early life stress as neonatal maternal deprivation (MD) predisposes rats to alter gut functions in response to acute psychological stressors in adulthood, mimicking features of irritable bowel syndrome (IBS). We applied proteomics to investigate whether MD permanently changes the protein profile of the external colonic neuromuscular layer that may condition the molecular response to an acute stressor later in life. Male rat pups were separated 3 h/day from their mothers during the perinatal period and further submitted to water avoidance (WA) stress during adulthood. Proteins were extracted from the myenteric plexus-longitudinal muscle of control (C), WA and MD+WA rat colon, separated on 2D gels, and identified by mass spectrometry. MD amplified the WA-induced protein changes involved in muscle contractile function, suggesting that stress accumulation along life imbalances the muscle tone towards hypercontractility. Our results also propose a stress dependent regulation of gluconeogenesis. Secretogranin II - the secretoneurin precursor - was induced by MD. The presence of secretoneurin in myenteric ganglia may partially explain the stress-mediated modulation of gastrointestinal motility and/or mucosal inflammation previously described in MD rats. In conclusion, our findings suggest that neonatal stress alters the responses to acute stress in adulthood in intestinal smooth muscle and enteric neurons.

MeSH terms

  • Animals
  • Animals, Newborn
  • Colon / metabolism*
  • Female
  • Gastrointestinal Motility
  • Gene Expression Profiling
  • Gene Expression Regulation*
  • Male
  • Maternal Deprivation*
  • Neuropeptides / metabolism
  • Rats
  • Rats, Long-Evans
  • Secretogranin II / metabolism
  • Stress, Physiological / physiopathology
  • Stress, Psychological / physiopathology*

Substances

  • Neuropeptides
  • Secretogranin II
  • secretoneurin