Exogenous Growth Differentiation Factor 15 (GDF15) exerts direct cardioprotective properties towards myocardial ischemia reperfusion injury
Abstract Funding Acknowledgements Type of funding sources: Public grant(s) – National budget only. Main funding source(s): Agence National de la Recherche (ANR) Introduction Growth differentiation factor 15 (GDF15) is a stress-responsive cytokine which can be produced under certain pathological situ...
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| Published in: | Cardiovascular research Vol. 118; no. Supplement_1 |
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| Main Authors: | , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
10-06-2022
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| Online Access: | Get full text |
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| Summary: | Abstract
Funding Acknowledgements
Type of funding sources: Public grant(s) – National budget only. Main funding source(s): Agence National de la Recherche (ANR)
Introduction
Growth differentiation factor 15 (GDF15) is a stress-responsive cytokine which can be produced under certain pathological situations, mainly related to inflammatory stress, aging and disease. While clinical data suggest that GDF15 is a powerful risk factor in several high cardiovascular risks situations such as myocardial infarction and coronary artery disease, experimental studies rather consider this cytokine as a cardioprotective molecule.
Objective
We therefore aimed to clarify the direct cardiac effects of GDF15 during ischemia-reperfusion (I-R) injury, at concentrations found in patients with high cardiovascular risk, such as these of patients presenting with acute myocardial infarction or stroke.
Method
In vivo ischemia reperfusion: Wistar male rats (200-340 g) were anesthetized with isoflurane and intubated before a left thoracotomy was performed between the 3rd and the 4th intercostal space. Rats were injected with either saline (Control groups) or 2.5 µg/kg of GDF15 (GDF15 groups), 20 minutes before the transient ligation of the left anterior descending artery for 30 min followed by 24h of reperfusion.
Ex vivo ischemia reperfusion: Wistar male rats (250-400 g) were anesthetized with isoflurane before their hearts were isolated and perfused in a Langendorff model. Hearts were perfused either with saline (Control groups) or 2,000 ng/L of GDF15 upstream the coronary bed (GDF15 groups) for 10 minutes, then subjected to either 20 or 30 minutes of global normothermic total ischemia, followed by 2 h of reperfusion.
Results
GDF15 decreased the infarct size in vivo (42.4 ± 6 % vs. 65.3 ± 4.5 %, p<0.01) as well as in ex vivo (45.6 ± 3.8 % vs. 60.8 ± 3.8 %, p<0.05). Moreover, in our ex vivo model, GDF15 induced a better recovery of most contractile parameters after ischemia (higher left ventricular developed pressure, better heart rate recovery, better recovery in left ventricular contractility and relaxation, p<0.05 for all parameters).
Conclusion
These results demonstrate for the first time that exogenous preischemic short-term administration of GDF15 decreased cardiac cell death in vivo and also ex vivo, a situation where inflammatory, endocrine and nervous systems are not interfering. These original results suggest that GDF15 exerts direct cardioprotective properties towards ischemia-reperfusion injury. The molecular mechanisms have now to be investigated. |
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| ISSN: | 0008-6363 1755-3245 |
| DOI: | 10.1093/cvr/cvac066.048 |