AI Article Synopsis
- Insulin administration during reperfusion has cardioprotective effects, potentially by acting on the sphingosine kinase/sphingosine 1-phosphate (S1P) pathway in cardiomyocytes.
- In experiments with rat cardiomyocytes, insulin increased sphingosine kinase activity, changed its location within cells, and raised S1P levels, which are needed to prevent cell death.
- The findings suggest that insulin reduces apoptosis due to hypoxia/reoxygenation injury by activating the S1P receptor, highlighting a novel protective mechanism for heart cells.
Article Abstract
Objective: Experimental and clinical studies have shown that administration of insulin during reperfusion is cardioprotective, but the mechanisms underlying this effect are still unknown. In this study, the ability of insulin to protect apoptotic cardiomyocytes from hypoxia/reoxygenation injury using the sphingosine kinase/sphingosine 1-phosphate axis was investigated.
Methods And Results: Rat cardiomyocytes were isolated and subjected to hypoxia and reoxygenation. [γ-32P] ATP was used to assess sphingosine kinase activity. Insulin was found to increase sphingosine kinase activity. Immunocytochemistry and Western blot analysis showed changes in the subcellular location of sphingosine kinase 1 from cytosol to the membrane in cardiomyocytes. Insulin caused cardiomyocytes to accumulate of S1P in a dose-dependent manner. FRET efficiency showed that insulin also transactivates the S1P1 receptor. TUNEL staining showed that administration of insulin during reoxygenation could to reduce the rate of reoxygenation-induced apoptosis, which is a requirement for SphK 1 activity. It also reduced the rate of activation of the S1P receptor and inhibited hypoxia/reoxygenation-induced cell death in cardiomyocytes.
Conclusion: The sphingosine kinase 1/sphingosine 1-phosphate/S1P receptor axis is one pathway through which insulin protects rat cardiomyocytes from apoptosis induced by hypoxia/reoxygenation injury.
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|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859498 | PMC |
| http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0080644 | PLOS |
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