Mitochondrial fusion proteins in revascularized hibernating hearts

Christopher T. Holley, Eric K. Long, Tammy A. Butterick, Cayla M. Duffy, Megan E. Lindsey, Laura Hocum Stone, Edward O. McFalls, Rosemary F. Kelly

Research output: Contribution to journalArticlepeer-review

4 Scopus citations


Background Hibernating myocardium is characterized by viable yet dysfunctional myocardium secondary to chronic ischemia, with studies demonstrating incomplete early recovery after coronary artery bypass graft (CABG). We tested whether mitochondrial fusion proteins, an indicator of mitochondrial biogenesis, are increased in hibernating myocardium post-CABG. Methods A constrictor was placed on the left anterior descending (LAD) artery of nine pigs. Four of these pigs additionally underwent CABG 12 wk later with a left internal mammary artery graft to the LAD distal to the constrictor. Five pigs had a constrictor placed but did not undergo CABG (Hib). Five pigs did not have a constrictor placed (control). Computerized tomography angiography was used to confirm stenosis at the site of constrictor placement and patency of left internal mammary artery grafts. Regional blood flows were determined at baseline and during 40 μg/kg/min dobutamine infusion. Mitochondrial proteins were quantified by Western blot. Results Blood flow in the LAD region after CABG was lower than remote regions during dobutamine infusion (2.54 ± 0.24 versus 3.46 ± 0.33 mL/min/g; P < 0.05). Electron transport chain proteins were ∼70% lower in Hib compared with those in control and failed to normalize after CABG. Post-CABG, PGC1α nuclear-bound content was increased compared with Hib (9.02 ± 0.48 versus 5.54 ± 0.98 arbitrary units, respectively; P < 0.05), and expression of mitofusins-1 and 2 and optic atrophy-1 more than doubled. Conclusions PGC1α and mitochondrial fusion proteins are increased 4 wk post-CABG in hibernating hearts, indicating mitochondrial fusion has begun to occur and signaling early mitochondrial recovery. Future studies should address changes in maximal myocardial oxygen consumption relative to mitochondrial protein expression.

Original languageEnglish (US)
Pages (from-to)29-36
Number of pages8
JournalJournal of Surgical Research
Issue number1
StatePublished - May 1 2015

Bibliographical note

Funding Information:
This work was supported in part by NIH (EOM, NIH-HLBI: R01HL089307 ) and VA Merit Review Grants (R.F.K.).

Funding Information:
This work was supported in part by NIH (EOM, NIH-HLBI: R01HL089307), and VA Merit Review Grants (R.F.K.).

Publisher Copyright:
© 2015 Elsevier Inc. All rights reserved.


  • Animal model of cardiovascular disease
  • Coronary artery bypass graft surgery
  • Hibernating myocardium
  • Ischemic heart disease
  • Mitochondrial disease cardiomyopathy


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