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1 Nutritional Physiology Group, Dapartment of Animal Science, Iowa State University, Ames 50011
A model ketosis can be produced in dairy cows by restricting feed intake plus feeding 1,3-butanediol. Increases in D-ß-hydroxybutyrate in blood result from metabolism of the 1,3-butanediol, but the site of metabolism has not been established. In vitro production of D-ß-hydroxybutyrate from butyrate and from isomers of 1,3-butanediol was measured in bovine liver, rumen papillae, and kidney cortex, all obtained at slaughter from nonlactating, nonpregnant Holstein cows. Production of D-ß-hydroxybutyrate from butyrate by the tissues was greatest for liver and rumen and much less for kidney. Only liver, however, produced appreciable amounts of D-ß-hydroxybutyrate from R-, S-, or RS-1,3-butanediol, and rates were maximal at substrate concentrations of 5 mM. Production of D-ß-hydroxybutyrate from R-1,3-butanediol by liver was greater than from S-1,3-butanediol. In vitro rates of production of D-ß-hydroxybutyrate were consistent with liver being the primary tissue involved in the metabolism of 1,3-butanediol, and capacity of the liver probably is sufficient to account for metabolism of 1,3-butanediol when 1 kg is fed daily to dairy cows.
Key Words: 1,3-butanediol liver ßbeta;-hydroxybutyrate
Submitted on May 24, 1989
Accepted on September 25, 1989
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