Literature DB >> 7226445

The utilization by rabbit aorta of carbohydrates, fatty acids, ketone bodies, and amino acids as substrates for energy production.

K V Chace, R Odessey.   

Abstract

The ability of rabbit aorta to oxidize various substrates was studied to determine which of these compounds may be energy substrates for vascular smooth muscle (VSM). Glucose, ketone bodies, medium-chain length fatty acids, branched-chain amino acids, and glutamine all are oxidized at comparable rates on a molar basis. Some other amino acids, long chain fatty acids, pyruvate and glycerol also are oxidized, but at lower rates. The oxidation of 6 amino acids could not be detected. VSM was found to release ketone bodies when incubated in leucine beta-hydroxybutyrate or octanoate. This suggests that the acetoacetyl CoA and/or acetoacetate derived from these substrates is not completely oxidized. The oxidation rate of several substrates when measured individually is inhibited by 50-80% by the presence of a combination of other substrates in the medium. Under these conditions, glucose is a minor substrate for oxidative metabolism accounting for only 5% of O2 consumption. The oxidation rate of all the exogenous substrates together is calculated to account for less than half of the oxygen consumption; this finding indicates that an endogenous substrate must also be utilized.

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Year:  1981        PMID: 7226445     DOI: 10.1161/01.res.48.6.850

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  9 in total

1.  The metabolic basis of vascular oxygen sensing: diversity, compartmentalization, and lessons from cancer.

Authors:  Evangelos D Michelakis; E Kenneth Weir
Journal:  Am J Physiol Heart Circ Physiol       Date:  2008-07-11       Impact factor: 4.733

Review 2.  Energy metabolism and transduction in smooth muscle.

Authors:  R M Lynch; R J Paul
Journal:  Experientia       Date:  1985-08-15

3.  Effect of palmitate on carbohydrate utilization and Na/K-ATPase activity in aortic vascular smooth muscle from diabetic rats.

Authors:  J M Smith; S M Solar; D J Paulson; N M Hill; T L Broderick
Journal:  Mol Cell Biochem       Date:  1999-04       Impact factor: 3.396

4.  Dissociation of K+-induced tension and cellular Ca2+ retention in vascular and intestinal smooth muscle in normoxia and hypoxia.

Authors:  H Karaki; T Suzuki; H Ozaki; N Urakawa; Y Ishida
Journal:  Pflugers Arch       Date:  1982-08       Impact factor: 3.657

5.  Alterations in the oxidative metabolic profile in vascular smooth muscle from hyperlipidemic and diabetic swine.

Authors:  T M Roberts; M Sturek; J L Dixon; C D Hardin
Journal:  Mol Cell Biochem       Date:  2001-01       Impact factor: 3.396

6.  Changes of glycogen and ATP contents of the major cerebral arteries after experimentally produced subarachnoid haemorrhage in the dog.

Authors:  K Nozaki; S Okamoto; Y Uemura; H Yanamoto; H Kikuchi
Journal:  Acta Neurochir (Wien)       Date:  1990       Impact factor: 2.216

7.  Endothelium-dependent inhibition of Na(+)-K+ ATPase activity in rabbit aorta by hyperglycemia. Possible role of endothelium-derived nitric oxide.

Authors:  S Gupta; I Sussman; C S McArthur; K Tornheim; R A Cohen; N B Ruderman
Journal:  J Clin Invest       Date:  1992-09       Impact factor: 14.808

Review 8.  Lipid metabolism of myocardial endothelial cells.

Authors:  K Schoonderwoerd; H Stam
Journal:  Mol Cell Biochem       Date:  1992-10-21       Impact factor: 3.396

Review 9.  Important Functions and Molecular Mechanisms of Mitochondrial Redox Signaling in Pulmonary Hypertension.

Authors:  Jorge Reyes-García; Abril Carbajal-García; Annarita Di Mise; Yun-Min Zheng; Xiangdong Wang; Yong-Xiao Wang
Journal:  Antioxidants (Basel)       Date:  2022-02-28
  9 in total

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