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Ann Thorac Surg 1991;52:14-19
© 1991 The Society of Thoracic Surgeons


Articles

Triiodothyronine-enhanced left ventricular function after ischemic injury

Cornelius M. Dyke, MD, Thomas Yeh, Jr, MD, Jonathan D. Lehman, BS, Anwar Abd-Elfattah, PhD, Mai Ding, MD, Andrew S. Wechsler, MD, David R. Salter, MD*

Department of Surgery, Medical College of Virginia, Virginia Commonwealth University, Richmond, Virginia USA

* Address reprint requests to Dr Salter, Hunter Holmes McGuire Veterans Medical Center, 1201 Broad Rock Blvd, Richmond, VA 23298.


    Abstract
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 Abstract
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Hypothyroidism is associated with profound left ventricular dysfunction. Brain-dead organ donors and patients undergoing cardiopulmonary bypass are chemically hypothyroid with significantly reduced circulating free triiodothyronine (T3). To test the hypothesis that T3 enhances left ventricular function in a hormonally deficient environment a total of 36 healthy New Zealand White rabbit hearts were studied using a modified Langendorff preparation with Krebs-Henseleit perfusate and intraventricular balloon. In 9 normal rabbit hearts a cumulative dose-response curve with logarithmically increasing doses of T3 was obtained. The vehicle solution for T3 dissolution served as control (n = 9). Left ventricular function was assessed from peak developed pressure at baseline and after T3 administration. Triiodothyronine had no effect in normal hearts on peak developed pressure or end-diastolic pressure. In 18 rabbits, the acute effect of T3 administration after ischemia was investigated. Preischemic left ventricular function was measured to serve as baseline, and hearts were subjected to 37 °C global ischemia. Triiodothyronine (n = 9) or vehicle (n = 9) was infused during reperfusion, and left ventricular peak developed pressure was measured at 30 and 60 minutes of reperfusion. Recovery of function (expressed as percent return of left ventricular peak developed pressure) was significantly improved within 15 minutes of reperfusion (65.0% ± 2.1% versus 80.2% ± 4.1%) and remained significantly improved throughout the reperfusion period (p < 0.05 by analysis of variance). These data suggest that although T3 possesses no inotropic properties, it significantly improves postischemic left ventricular function. The rapidity of the functional improvement suggests that these effects may be due to plasma membrane-mediated mechanisms.


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{star} Presented at the Twenty-seventh Annual Meeting of The Society of Thoracic Surgeons, San Francisco, CA, Feb 18–20, 1991.

{star}{star} This study was supported in part by grant HL 26302-11 from the National Institutes of Health and by a Small Grants Award from the Medical College of Virginia.


    References
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 Abstract
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 References
 

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