Summary
Acetate derived from ethanol oxidation is activated by cytosolic and mitochondrial acetyl-CoA synthetases before contributing to the extra-mitochondrial processes of fatty acid and 3-β-hydroxysterol synthesis. Mitochondrially-generated acetyl-CoA is transferred to the cytosol via citrate and ATP-citrate lyase; this transfer is blocked by (-)-hydroxycitrate. Rats were injected IV with 3.3 mmol/kg of [2-3H,2-14C] acetate and IP with either 0.5 mmol/kg hydroxycitrate or saline. After one hour, the rats were killed and the incorporation of label was measured in liver fatty acids and 3-β-hydroxysterols. The 3H/14C ratio was increased by 12 and 13% in the fatty acids and 3-β-hydroxysterols of the hydroxycitrate-treated group. The lower ratio in the fatty acids and 3-β-hydroxysterols derived from mitochondrially-generated acetylCoA is ascribed to a loss of 3H in the citrate synthase reaction. The data showed that (1) fatty acids and 3-β-hydroxysterols syntheses use the same pool of cytosolic acetyl-CoA; and (2) in the absence of an isotope effect in the citrate synthase reaction, mitochondrially-generated acetyl-CoA contributes about 36% to lipogenesis from acetate.
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References
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© 1980 Springer Science+Business Media New York
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Goldberg, R.P., Brunengraber, H. (1980). Contributions of Cytosolic and Mitochondrial Acetyl-CoA Syntheses to the Activation of Lipogenic Acetate in Rat Liver. In: Thurman, R.G. (eds) Alcohol and Aldehyde Metabolizing Systems-IV. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-1419-7_41
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DOI: https://doi.org/10.1007/978-1-4757-1419-7_41
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