Protein carbonylation causes sarcoplasmic reticulum Ca(2+) overload by increasing intracellular Na(+) level in ventricular myocytes.

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作者:Bovo Elisa, Seflova Jaroslava, Robia Seth L, Zima Aleksey V
Diabetes is commonly associated with an elevated level of reactive carbonyl species due to alteration of glucose and fatty acid metabolism. These metabolic changes cause an abnormality in cardiac Ca(2+) regulation that can lead to cardiomyopathies. In this study, we explored how the reactive α-dicarbonyl methylglyoxal (MGO) affects Ca(2+) regulation in mouse ventricular myocytes. Analysis of intracellular Ca(2+) dynamics revealed that MGO (200 μM) increases action potential (AP)-induced Ca(2+) transients and sarcoplasmic reticulum (SR) Ca(2+) load, with a limited effect on L-type Ca(2+) channel-mediated Ca(2+) transients and SERCA-mediated Ca(2+) uptake. At the same time, MGO significantly slowed down cytosolic Ca(2+) extrusion by Na(+)/Ca(2+) exchanger (NCX). MGO also increased the frequency of Ca(2+) waves during rest and these Ca(2+) release events were abolished by an external solution with zero [Na(+)] and [Ca(2+)]. Adrenergic receptor activation with isoproterenol (10 nM) increased Ca(2+) transients and SR Ca(2+) load, but it also triggered spontaneous Ca(2+) waves in 27% of studied cells. Pretreatment of myocytes with MGO increased the fraction of cells with Ca(2+) waves during adrenergic receptor stimulation by 163%. Measurements of intracellular [Na(+)] revealed that MGO increases cytosolic [Na(+)] by 57% from the maximal effect produced by the Na(+)-K(+) ATPase inhibitor ouabain (20 μM). This increase in cytosolic [Na(+)] was a result of activation of a tetrodotoxin-sensitive Na(+) influx, but not an inhibition of Na(+)-K(+) ATPase. An increase in cytosolic [Na(+)] after treating cells with ouabain produced similar effects on Ca(2+) regulation as MGO. These results suggest that protein carbonylation can affect cardiac Ca(2+) regulation by increasing cytosolic [Na(+)] via a tetrodotoxin-sensitive pathway. This, in turn, reduces Ca(2+) extrusion by NCX, causing SR Ca(2+) overload and spontaneous Ca(2+) waves.

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