The Journal of Thoracic and Cardiovascular Surgery
Volume 139, Issue 4 , Pages 1057-1063, April 2010

Prolonged donor heart preservation with pinacidil: The role of mitochondria and the mitochondrial adenosine triphosphate–sensitive potassium channel

  • Liuqing Yang, MD

      Affiliations

    • Department of Anesthesiology, Zunyi Medical College, Zunyi, China
    • Subei People's Hospital of Jiangsu Province, Yangzhou, China
  • ,
  • Tian Yu, MD, PhD

      Affiliations

    • Department of Anesthesiology, Zunyi Medical College, Zunyi, China
    • Corresponding Author InformationAddress for reprints: Tian Yu, MD, PhD, Department of Anesthesiology, Zunyi Medical College, Dalian road 201, Zunyi City, 563000, Guizhou Province, People's Republic of China.

Received 2 April 2009; received in revised form 28 September 2009; accepted 25 October 2009.

Objective

Prolonged donor heart preservation is important in cardiovascular surgery. This study examined the effect of pinacidil, a nonselective adenosine triphosphate–sensitive potassium channel opener, on donor heart preservation when added to histidine tryptophan ketoglutarate solution and the role of mitochondria in this protection.

Methods

Sprague–Dawley rat hearts received one of 5 preservation solutions in the Langendorff perfusion apparatus (24 per group): (1) histidine tryptophan ketoglutarate solution; (2) histidine tryptophan ketoglutarate solution containing pinacidil; (3) histidine tryptophan ketoglutarate solution containing pinacidil and 5-hydroxydecanote, a mitochondrial adenosine triphosphate–sensitive potassium channel blocker; (4) histidine tryptophan ketoglutarate solution containing pinacidil and Hoechst–Marion–Roussel 1098, a sarcolemmal adenosine triphosphate–sensitive potassium channel blocker; and (5) histidine tryptophan ketoglutarate solution containing pinacidil, 5-hydroxydecanote, and Hoechst–Marion–Roussel 1098. After a 10-minute equilibration period, all the hearts in the different preservation solutions were placed in cold storage for 8 hours, followed by 60 minutes of reperfusion. Hemodynamics, mitochondrial respiratory function, adenosine triphosphate level, cardiac troponin I release, and ultrastructure were examined.

Results

Histidine tryptophan ketoglutarate solution containing 0.5 mmol/L pinicidal significantly improved heart function, coronary flow, myocardial ultrastructure, and cardiac troponin I release after reperfusion (P < .01 or P < .05). In the pinacidil group at the end of storage and the end of reperfusion, mitochondrial respiratory function and myocardial adenosine triphosphate levels were superior when compared with other groups (P < .01 or P < .05). These beneficial effects of pinacidil were blocked by 100 μmol/L 5-hydroxydecanote.

Conclusion

Histidine tryptophan ketoglutarate solution containing pinacidil provides better cardioprotection with preservation of mitochondrial energy. This effect of pinacidil appears to depend on both mitochondrial and sarcolemmal adenosine triphosphate sensitive potassium channel.

CTSNet classification: 34

Abbreviations and Acronyms: ADP, adenosine diphosphate, ATP, adenosine triphosphate, CF, coronary flow, cTnI, cardiac troponin I, 5HD, 5-Hydroxydecanote, HMR1098, Hoechst–Marion–Roussel 1098, HR, heart rate, HTK, histidine tryptophan ketoglutarate, KATP, adenosine triphosphate–sensitive potassium, K–H, Krebs–Henseleit, LVDP, left ventricular developed pressure, LVEDP, left ventricular end-diastolic pressure, mitoKATP, mitochondrial adenosine triphosphate–sensitive potassium, sarcKATP, sarcolemmal adenosine triphosphate–sensitive potassium, S3, state 3 respiration, S4, state 4 respiration, Tris–HCl, tris-(hydroxymethyl)-aminomethane hydrochloride

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 Supported by the Chinese National Natural Science Foundation (no. 30460132).

 Disclosures: None.

PII: S0022-5223(09)01409-3

doi:10.1016/j.jtcvs.2009.10.042

The Journal of Thoracic and Cardiovascular Surgery
Volume 139, Issue 4 , Pages 1057-1063, April 2010