In: Journal of Cardiothoracic Surgery, 5 (2010), Nr. 106. pp. 1-6. ISSN 1749-8090
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Abstract
Objective: Inosine, a break-down product of adenosine has been recently shown to exert inodilatory and anti-inflammatory properties. Furthermore inosine might be a key substrate of pharmacological post-conditioning. In the present pre-clinical study, we investigated the effects of inosine on cardiac function during reperfusion in an experimental model of cardioplegic arrest and extracorporal circulation. Methods: Twelve anesthetized dogs underwent hypothermic cardiopulmonary bypass. After 60 minutes of hypothermic cardiac arrest, reperfusion was started after application of either saline vehicle (control, n = 6), or inosine (100 mg/kg, n = 6). Left ventricular end-systolic pressure volume relationship (ESPVR) was measured by a combined pressure-volume-conductance catheter at baseline and after 60 minutes of reperfusion. Left anterior descendent coronary blood flow (CBF), endothelium-dependent vasodilatation to acetylcholine (ACh) and endothelium-independent vasodilatation to sodium nitroprusside (SNP) were also determined. Results: The administration of inosine led to a significantly better recovery (given as percent of baseline) of ESPVR 90 ± 9% vs. 46 ± 6%, p < 0.05. CBF and was also significantly higher in the inosine group (56 ± 8 vs. 23 ± 4, ml/min, p < 0.05). While the vasodilatatory response to SNP was similar in both groups, ACh resulted in a significantly higher increase in CBF (58 ± 6% vs. 25 ± 5%, p < 0.05) in the inosine group. Conclusions: Application of inosine improves myocardial and endothelial function after cardiopulmonary bypass with hypothermic cardiac arrest.
| Document type: | Article |
|---|---|
| Journal or Publication Title: | Journal of Cardiothoracic Surgery |
| Volume: | 5 |
| Number: | 106 |
| Publisher: | BioMed Central |
| Place of Publication: | London |
| Date Deposited: | 25 Jan 2016 08:07 |
| Date: | 2010 |
| ISSN: | 1749-8090 |
| Page Range: | pp. 1-6 |
| Faculties / Institutes: | Medizinische Fakultät Heidelberg > Chirurgische Universitätsklinik |
| DDC-classification: | 610 Medical sciences Medicine |








