Effect of germfree state on the capacities of isolated rat colonocytes to metabolize n-butyrate, glucose, and glutamine

Gastroenterology. 1995 Dec;109(6):1890-9. doi: 10.1016/0016-5085(95)90756-4.

Abstract

Background & aims: Among substrates available to the colonic mucosa, n-butyrate from bacterial origin represents a major fuel. The present work investigated possible modifications of energy substrate metabolism in colonocytes isolated from germfree rats.

Methods: Colonocytes isolated from germfree vs. conventional rats were incubated (30 minutes at 37 degrees C) in the presence of 14C-labeled n-butyrate (10 mmol/L), glucose (5 mmol/L), or glutamine (5 mmol/L). 14CO2 and metabolites generated were measured. Possible regulatory steps were also investigated.

Results: Glucose use rate was 25% lower in germfree rat colonocytes due to a reduced glycolytic capacity in these cells. Differences in 6-phosphofructo-1-kinase activity could account for this decrease. In contrast, glutamine use rate was 45% higher, and this was correlated with a higher maximum velocity of glutaminase in these cells. Nevertheless, the capacities to oxidize glucose and glutamine remained unchanged. Although the capacity to use n-butyrate was maintained in colonocytes of germfree rats, the ketogenic capacity was lower, whereas the capacity to oxidize n-butyrate was higher. The mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme A synthase protein was identified in the colonic mucosa. Moreover, the messenger RNA and amount of protein were 75% lower in the germfree state.

Conclusions: The absence of an intestinal microflora induces specific changes in the metabolic capacities of colonocytes.

MeSH terms

  • Animals
  • Butyrates / metabolism*
  • Cells, Cultured
  • Colon / cytology
  • Colon / enzymology
  • Colon / metabolism*
  • Germ-Free Life*
  • Glucose / metabolism*
  • Glutaminase / metabolism
  • Glutamine / metabolism*
  • Hydroxymethylglutaryl-CoA Synthase / genetics
  • Hydroxymethylglutaryl-CoA Synthase / metabolism
  • Intestinal Mucosa / enzymology
  • Male
  • Mitochondria / enzymology
  • Oxidation-Reduction
  • Phosphofructokinase-1 / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred F344

Substances

  • Butyrates
  • RNA, Messenger
  • Glutamine
  • Hydroxymethylglutaryl-CoA Synthase
  • Phosphofructokinase-1
  • Glutaminase
  • Glucose