TY - JOUR
T1 - Adaptive increase in pyruvate dehydrogenase kinase 4 during starvation is mediated by peroxisome proliferator-activated receptor α
AU - Wu, Pengfei
AU - Peters, Jeffrey M.
AU - Harris, Robert A.
N1 - Funding Information:
The authors gratefully acknowledge Frank Gonzalez for providing the PPARα-null mice for this work. Support was provided by grants from NIH (DK47844) and the American Heart Association (0051370Z).
PY - 2001/9/21
Y1 - 2001/9/21
N2 - Pyruvate dehydrogenase kinase isoform 4 (PDK4) is upregulated by starvation in many tissues of the body during starvation. This causes inactivation of the pyruvate dehydrogenase complex which blocks pyruvate oxidation and conserves lactate and alanine for gluconeogenesis. Enhanced PDK4 expression may be caused by the increase in free fatty acids that occurs during starvation. Free fatty acids can activate peroxisome proliferator-activated receptor α (PPARα), and activation of PPARα can promote PDK4 expression. This model is supported by the findings reported here that WY-14,643, a synthetic PPARα activator, increases PDK4 expression in wild-type mice but not in PPARα-null mice. Starvation likewise increases the expression of PDK4 in tissues of wild-type mice but not in tissues of PPARα,-null mice. These findings document the functional importance of PPARα, for PDK4 expression during starvation and suggest an important role for elevated free fatty acids in the induction.
AB - Pyruvate dehydrogenase kinase isoform 4 (PDK4) is upregulated by starvation in many tissues of the body during starvation. This causes inactivation of the pyruvate dehydrogenase complex which blocks pyruvate oxidation and conserves lactate and alanine for gluconeogenesis. Enhanced PDK4 expression may be caused by the increase in free fatty acids that occurs during starvation. Free fatty acids can activate peroxisome proliferator-activated receptor α (PPARα), and activation of PPARα can promote PDK4 expression. This model is supported by the findings reported here that WY-14,643, a synthetic PPARα activator, increases PDK4 expression in wild-type mice but not in PPARα-null mice. Starvation likewise increases the expression of PDK4 in tissues of wild-type mice but not in tissues of PPARα,-null mice. These findings document the functional importance of PPARα, for PDK4 expression during starvation and suggest an important role for elevated free fatty acids in the induction.
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U2 - 10.1006/bbrc.2001.5608
DO - 10.1006/bbrc.2001.5608
M3 - Article
C2 - 11554740
AN - SCOPUS:0035929170
SN - 0006-291X
VL - 287
SP - 391
EP - 396
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -