Journal of Lipid Research (Nov 2007)

Dietary n-3 PUFA deprivation for 15 weeks upregulates elongase and desaturase expression in rat liver but not brain

  • Miki Igarashi,
  • Kaizong Ma,
  • Lisa Chang,
  • Jane M. Bell,
  • Stanley I. Rapoport

Journal volume & issue
Vol. 48, no. 11
pp. 2463 – 2470

Abstract

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Fifteen weeks of dietary n-3 PUFA deprivation increases coefficients of conversion of circulating α-linolenic acid (α-LNA; 18:3n-3) to docosahexaenoic acid (DHA; 22:6n-3) in rat liver but not brain. To determine whether these increases reflect organ differences in enzymatic activities, we examined brain and liver expression of converting enzymes and of two of their transcription factors, peroxisome proliferator-activated receptor α (PPARα) and sterol-regulatory element binding protein-1 (SREBP-1), in rats fed an n-3 PUFA “adequate” (4.6% α-LNA of total fatty acid, no DHA) or “deficient” (0.2% α-LNA, no DHA) diet for 15 weeks after weaning. In rats fed the deficient compared with the adequate diet, mRNA and activity levels of Δ5 and Δ6 desaturases and elongases 2 and 5 were upregulated in liver but not brain, but liver PPARα and SREBP-1 mRNA levels were unchanged. In rats fed the adequate diet, enzyme activities generally were higher in liver than brain. Thus, differences in conversion enzyme expression explain why the liver has a greater capacity to synthesize DHA from circulating α-LNA than does the brain in animals on an adequate n-3 PUFA diet and why liver synthesis capacity is increased by dietary deprivation. These data suggest that liver n-3 PUFA metabolism determines DHA availability to the brain when DHA is absent from the diet.

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