Effects of dl-2-hydroxy-4-methylthiobutyrate on the first-pass intestinal metabolism of dietary methionine and its extra-intestinal availability

Br J Nutr. 2010 Mar;103(5):643-51. doi: 10.1017/S0007114509992169. Epub 2010 Jan 12.

Abstract

The present study was conducted in a one-factorial arrangement to determine the effects of dl-2-hydroxy-4-methylthiobutyrate (dl-HMTB) on the first-pass intestinal metabolism of dietary methionine and its extra-intestinal availability. Barrows (n 6; aged 35 d; weight 8.6 kg), implanted with arterial, portal, mesenteric and gastric catheters, were fed a diet containing dl-methionine (dl-MET) or dl-HMTB once hourly and infused intramesenterically with 1 % p-aminohippurate and intragastrically with [1-13C]methionine at 7.0 mumol/kg body weight per h. Arterial and portal blood samples were taken at hourly intervals until 6 h of tracer infusion and pigs was then killed for collection of muscle, intestine, liver and kidney samples. The net portal appearance of methionine, expressed as the fraction of ingested directly available l-methionine, was higher (P < 0.05) in the dl-HMTB than in the dl-MET diet, and there was no difference (P = 0.26) in the fractional portal balance of [1-13C]methionine between the diets. [1-13C]methionine enrichment (tracer:tracee ratio; mol/100 mol amino acid) in the jejunum, arterial and portal plasma, liver, kidney and muscle was also not different (P>0.05) between the groups. Over the 6 h period after the start of feeding, the average concentration of citrulline both in the arterial and portal plasma was higher (P < 0.05) in the dl-HMTB than in the dl-MET group, and arterial plasma ornithine and taurine concentration was also higher (P < 0.05) in the dl-HMTB than in the dl-MET group. However, plasma urea concentration both in the arterial and portal vein was lower (P < 0.05) in the dl-HMTB than in the dl-MET group. These results suggested that the potential difference in the first-pass use of methionine by the intestine between the dl-HMTB and dl-MET diets might affect intestinal and systemic metabolism of other amino acids, which may provide new important insights into nutritional efficiency of different methionine sources.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / blood
  • Animals
  • Diet*
  • Dietary Proteins / metabolism*
  • Intestinal Absorption / physiology
  • Intestine, Small / metabolism*
  • Kidney / metabolism
  • Liver / metabolism
  • Methionine / analogs & derivatives*
  • Methionine / blood
  • Methionine / metabolism*
  • Muscles / metabolism
  • Portal System / metabolism
  • Swine
  • Urea / blood
  • p-Aminohippuric Acid

Substances

  • Amino Acids
  • Dietary Proteins
  • alpha-hydroxy-gamma-methylmercaptobutyric acid
  • Urea
  • Methionine
  • p-Aminohippuric Acid