Literature DB >> 3081512

Pathways of acetone's metabolism in the rat.

K Kosugi, R F Scofield, V Chandramouli, K Kumaran, W C Schumann, B R Landau.   

Abstract

Distributions of 14C were different from those of 13C in glucoses formed by livers of rats in diabetic ketosis and perfused with [2-14C]acetone and [2-13C]lactate. There was 32-73% of the 14C and 8-12% of the 13C in carbons 3 and 4 of the glucoses with the remaining 14C and 13C distributed about equally in the other carbons. Incorporations of 14C from [2-14C]acetone (14-39%) also exceeded those from [2-14C]pyruvate (8-10%) into carbons 3 and 4 of glucoses formed by hepatocytes from rats fed acetone or fasted. [2-14C]Acetone and [2-14C]pyruvate were infused into rats that were fed, fasted, given acetone in their drinking water, or in diabetic ketosis. Thirty-seven to 52% of the 14C in the glucoses formed was in their carbons 3 and 4 when the acetone was infused and 8 to 14% when the pyruvate was infused. [1,3-14C]Hydroxybutyrate was formed by the rats in diabetic ketosis given [2-14C]acetone. It is concluded that acetone is metabolized in rats to a large extent by a pathway in which lactate or its metabolic equivalent is not an intermediate and that pathway is via acetyl-CoA. via acetyl-CoA.

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Year:  1986        PMID: 3081512

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  5 in total

Review 1.  The biochemistry of diabetes.

Authors:  R Taylor; L Agius
Journal:  Biochem J       Date:  1988-03-15       Impact factor: 3.857

2.  NMR metabolomic study of blood plasma in ischemic and ischemically preconditioned rats: an increased level of ketone bodies and decreased content of glycolytic products 24 h after global cerebral ischemia.

Authors:  Eva Baranovicova; Marian Grendar; Dagmar Kalenska; Anna Tomascova; Daniel Cierny; Jan Lehotsky
Journal:  J Physiol Biochem       Date:  2018-05-11       Impact factor: 4.158

3.  Estimates of Krebs cycle activity and contributions of gluconeogenesis to hepatic glucose production in fasting healthy subjects and IDDM patients.

Authors:  B R Landau; V Chandramouli; W C Schumann; K Ekberg; K Kumaran; S C Kalhan; J Wahren
Journal:  Diabetologia       Date:  1995-07       Impact factor: 10.122

4.  Determination of Krebs cycle metabolic carbon exchange in vivo and its use to estimate the individual contributions of gluconeogenesis and glycogenolysis to overall glucose output in man.

Authors:  A Consoli; F Kennedy; J Miles; J Gerich
Journal:  J Clin Invest       Date:  1987-11       Impact factor: 14.808

5.  Direct evidence of iNOS-mediated in vivo free radical production and protein oxidation in acetone-induced ketosis.

Authors:  Krisztian Stadler; Marcelo G Bonini; Shannon Dallas; Danielle Duma; Ronald P Mason; Maria B Kadiiska
Journal:  Am J Physiol Endocrinol Metab       Date:  2008-06-17       Impact factor: 4.310

  5 in total

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