SR calcium depletion following reversal of the Na+/Ca2+-exchanger in rat ventricular myocytes

Citation
A. Baartscheer et al., SR calcium depletion following reversal of the Na+/Ca2+-exchanger in rat ventricular myocytes, J MOL CEL C, 32(6), 2000, pp. 1025-1037
Citations number
56
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
ISSN journal
00222828 → ACNP
Volume
32
Issue
6
Year of publication
2000
Pages
1025 - 1037
Database
ISI
SICI code
0022-2828(200006)32:6<1025:SCDFRO>2.0.ZU;2-P
Abstract
We previously reported that cytosolic calcium transiently increases after r eversal of the sarcolemmal Na+/Ca2+ exchanger. Calcium released from sarcop lasmic reticulum (SR) constituted the major part of this cytosolic transien t. The aim of this study was to test whether reversal of the Na+/Ca2+-excha nger affects SR calcium content, and whether altered SR calcium content is associated with direct triggering of SR calcium release or calcium release secondary to SR calcium overload. To this purpose we studied the change of SR calcium content after reversal of the Na+/Ca2+-exchanger and the depende nce on the magnitude of change of its free energy (Delta G(exch)) in isolat ed rat ventricular myocytes. The Na+/Ca2+-exchanger was reversed by abrupt reduction of extracellular so dium ([Na+](o)). The magnitude of change of Delta G(exch) was varied with [ Na+](o). Cytosolic free calcium ([Ca2+](i)) was measured with indo-1 and SR calcium content was estimated from the increase of [Ca2+](i) after rapid c ooling (RC). SR function was manipulated either by blockade of the SR Ca2+- ATPase with thapsigargin or by blockade of SR calcium release channels with tetracaine. Reversal of the Na+/Ca2+-exchanger caused a transient increase of [Ca2+](i) of about: 180 s duration with a time to peak of about 30 s. During the fir st 30 s rapid small amplitude cytosolic calcium fluctuations were superimpo sed on this transient. The magnitude of the response of [Ca2+](i) to RC, du ring the course of the cytosolic [Ca2+](i) transient, also transiently incr eased from 174 in control myocytes to 480 nmol/l at the time of the peak va lue. After correction of [Ca2+](i) data for the fraction of mitochondrially compartmentalized indo-1 and mitochondrial calcium, total calcium released from SR after RC was calculated with the use of literature data on cytosol ic calcium buffer capacity. Contrary to the measured RC-dependent increase of measured [Ca2+](i), after reversal of the Na+/Ca2+-exchanger, calculated total calcium released from SR transiently decreased. The extent of SR cal cium depletion after reversal of the Na+/Ca2+-exchanger increased with the magnitude of change of Delta G(exch). Restitution of [Na+](o) 30 s after re versal of the Na+/Ca2+-exchanger, greatly accelerated both recovery of [Ca2 +](i) and SR calcium content. Pretreatment of myocytes with thapsigargin ca used almost entire depletion of SR and substantial reduction of the cytosol ic transient of [Ca2+](i) following reversal of the Na+/Ca2+-exchanger. App lication of tetracaine hardly affected SR calcium content, but caused an in crease of the SR calcium content following reversal of the Na+/Ca2+-exchang er, while the cytosolic transient increase of [Ca2+](i) was substantially r educed. We conclude that reversal of the Na+/Ca2+-exchanger directly trigge rs SR calcium release and decreases SR calcium content in a Delta G(exch) d ependent manner. (C) 2000 Academic Press.