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March 1, 1993AJP Heart and Circulatory Physiology

Competition between palmitate and ketone bodies as fuels for the heart: study with positron emission tomography

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Key result

Infusion of 3-hydroxybutyrate significantly decreased the relative size of the early rapid phase of myocardial palmitate clearance by 28% (P<0.001), indicating reduced fatty acid oxidation.

Why the study?

Does infusion of 3-hydroxybutyrate inhibit myocardial fatty acid oxidation in vivo in humans and dogs?

Population

6 fasted human volunteers and 6 instrumented dogs

Comparison

Infusion of 3-hydroxybutyrate vs Baseline (before infusion)

Design

Other

Authors

JVJean‐Louis VanoverscheldeCardiac Imaging
William Wijns
William WijnsInterventional Cardiology
JKJ KolanowskiNorthwestern University

Discussion

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Overview

May support ketone-mediated shifts in myocardial substrate use; hypothesis-generating and should not yet change practice.

Structured PICO

Does infusion of 3-hydroxybutyrate inhibit myocardial fatty acid oxidation in vivo in humans and dogs?

P
Population
6 fasted human volunteers and 6 instrumented dogs studied to assess myocardial clearance kinetics before and during 3-hydroxybutyrate infusion.
I
Intervention
Infusion of 3-hydroxybutyrate (17 mumol.kg-1 x min-1)
C
Comparator
Baseline (before infusion)
O
Outcome
Myocardial clearance kinetics of [1-11C]palmitate assessed with positron emission tomography (size, half time, and index of the early rapid phase)surrogate

Main Result

Effect estimate: -28% change

p-value: p=<0.001

Infusion of 3-hydroxybutyrate alters palmitate kinetics in vivo by decreasing myocardial long-chain fatty acid oxidation and increasing backdiffusion of nonmetabolized tracer.

Cite This Study

Vanoverschelde et al. (1993) studied Fasted state (n=12). 3-hydroxybutyrate vs. Baseline (before infusion) was evaluated on Relative size of the early rapid phase of 11C myocardial clearance (-28% change, p=<0.001). Infusion of 3-hydroxybutyrate significantly decreased the relative size of the early rapid phase of myocardial palmitate clearance by 28% (P<0.001), indicating reduced fatty acid oxidation.

synapsesocial.com/papers/6aa251e00fc92d3596e564d6https://doi.org/10.1152/ajpheart.1993.264.3.h701
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Effects of inhibition of fatty acid oxidation on myocardial kinetics of 11C-labeled palmitate.1989 · 24 citations
  2. 2External assessment of myocardial metabolism with [11C]palmitate in rabbit hearts1979 · 45 citations
  3. 3β-Hydroxybutyrate inhibits myocardial fatty acid oxidation in vivo independent of changes in malonyl-CoA content2003 · 81 citations
  4. 4Evaluation of Fatty Acid .BETA.-Oxidation in Patients With Prior Myocardial Infarction in Relation to Myocardial Blood Flow, Total Oxidative Metabolism, and Left Ventricular Wall Motion2005 · 13 citations
  5. 5Kinetic models for analysing myocardial [11C]palmitate data2009 · 22 citations