RATE OF DIASTOLIC CA RELEASE FROM THE SARCOPLASMIC-RETICULUM OF INTACT RABBIT AND RAT VENTRICULAR MYOCYTES

Citation
Ra. Bassani et Dm. Bers, RATE OF DIASTOLIC CA RELEASE FROM THE SARCOPLASMIC-RETICULUM OF INTACT RABBIT AND RAT VENTRICULAR MYOCYTES, Biophysical journal, 68(5), 1995, pp. 2015-2022
Citations number
41
Categorie Soggetti
Biophysics
Journal title
ISSN journal
00063495
Volume
68
Issue
5
Year of publication
1995
Pages
2015 - 2022
Database
ISI
SICI code
0006-3495(1995)68:5<2015:RODCRF>2.0.ZU;2-S
Abstract
The sarcoplasmic reticulum (SR) of cardiac myocytes loses Ca during re st. In the present study, we estimated the rest-dependent unidirection al Ca efflux from the SR in intact rabbit and rat ventricular myocytes . We determined the time course of depletion of the SR Ca content (ass essed as the amount of Ca released by caffeine) after inhibition of th e SR Ca-ATPase by thapsigargin. Before rest intervals in Na-containing , Ca-free solution, a 3-min preperfusion with ONa,OCa solution was per formed to deplete Na-i but keep the SR Ca content constant. The decrea se in Na-i should stimulate Ca efflux via Na/Ca exchange when Na-o is reintroduced. Thapsigargin treatment was limited to the last 2 min of preperfusion with ONa,OCa solution to minimize SR Ca loss before addit ion of Na, while attaining complete block of the SR Ca pump. Total SR Ca content was estimated from the [Ca](i) transient evoked by caffeine , taking into account passive cellular Ca buffering. The time constant s for SR Ca loss after thapsigargin were 385 and 355 s, whereas the pr e-rest SR Ca content was estimated to be 106 and 114 mu M (mu mol/l no nmitochondrial cell volume) in rabbit and rat myocytes, respectively. The unidirectional Ca efflux from the SR was similar in the two cell t ypes (rabbit: 0.27 mu M s(-1); rat: 0.32 mu M s(-1)). These values are also comparable with that estimated from elementary Ca release events (''Ca sparks,'' 0.2-0.8 mu M s(-1)). Thus, resting leak of Ca from SR may be primarily via occasional openings of SR Ca release channels. F inally, this flux is very slow compared with other Ca transporters in ventricular myocytes.