Hepatic very-low-density lipoprotein and apolipoprotein B production are increased following in vivo induction of betaine-homocysteine S-methyltransferase

Biochem J. 2006 Apr 15;395(2):363-71. doi: 10.1042/BJ20051966.

Abstract

We have previously reported a positive correlation between the expression of BHMT (betaine-homocysteine S-methyltransferase) and ApoB (apolipoprotein B) in rat hepatoma McA (McArdle RH-7777) cells [Sowden, Collins, Smith, Garrow, Sparks and Sparks (1999) Biochem. J. 341, 639-645]. To examine whether a similar relationship occurs in vivo, hepatic BHMT expression was induced by feeding rats a Met (L-methionine)-restricted betaine-containing diet, and parameters of ApoB metabolism were evaluated. There were no generalized metabolic abnormalities associated with Met restriction for 7 days, as evidenced by control levels of serum glucose, ketones, alanine aminotransferase and L-homocysteine levels. Betaine plus the Met restriction resulted in lower serum insulin and non-esterified fatty acid levels. Betaine plus Met restriction induced hepatic BHMT 4-fold and ApoB mRNA 3-fold compared with Met restriction alone. No changes in percentage of edited ApoB mRNA were observed on the test diets. An increase in liver ApoB mRNA correlated with an 82% and 46% increase in ApoB and triacylglycerol production respectively using in vivo Triton WR 1339. Increased secretion of VLDL (very-low-density lipoprotein) with Met restriction plus betaine was associated with a 45% reduction in liver triacylglycerol compared with control. Nuclear run-off assays established that transcription of both bhmt and apob genes was also increased in Met-restricted plus betaine diets. No change in ApoB mRNA stability was detected in BHMT-transfected McA cells. Hepatic ApoB and BHMT mRNA levels were also increased by 1.8- and 3-fold respectively by betaine supplementation of Met-replete diets. Since dietary betaine increased ApoB mRNA, VLDL ApoB and triacylglycerol production and decreased hepatic triacylglycerol, results suggest that induction of apob transcription may provide a potential mechanism for mobilizing hepatic triacylglycerol by increasing ApoB available for VLDL assembly and secretion.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aging
  • Animals
  • Apolipoproteins B / biosynthesis*
  • Apolipoproteins B / genetics
  • Betaine / pharmacology
  • Betaine-Homocysteine S-Methyltransferase / biosynthesis
  • Betaine-Homocysteine S-Methyltransferase / genetics
  • Betaine-Homocysteine S-Methyltransferase / metabolism*
  • Diet
  • Enzyme Induction
  • Gene Expression Regulation, Developmental / drug effects
  • Growth and Development
  • Lipoproteins, VLDL / biosynthesis*
  • Liver / enzymology*
  • Male
  • Methionine / deficiency
  • RNA Stability / genetics
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Sterol Regulatory Element Binding Proteins / genetics
  • Transcription, Genetic / genetics

Substances

  • Apolipoproteins B
  • Lipoproteins, VLDL
  • RNA, Messenger
  • Sterol Regulatory Element Binding Proteins
  • Betaine
  • Methionine
  • Betaine-Homocysteine S-Methyltransferase