Literature DB >> 9633918

Regulation of mitochondrial [NADH] by cytosolic [Ca2+] and work in trabeculae from hypertrophic and normal rat hearts.

R Brandes1, L S Maier, D M Bers.   

Abstract

Pressure overload hypertrophy has previously been shown to reduce contractility but paradoxically to increase O2 consumption rates at a given force. Because O2 consumption rates are related to mitochondrial [NADH] ([NADH]m), we tested the hypothesis that with hypertrophy, control of [NADH]m may be altered. Left ventricular trabeculae were isolated from banded and control rat hearts, and fluorescence spectroscopy was used to monitor [NADH]m and cytosolic [Ca2+] ([Ca2+]c). The hearts from banded rats developed hypertrophy (heart-to-body weight ratio increased from 4.1+/-0.1 to 4.9+/-0.1 mg/g) and hypertension (systolic arterial pressure increased from 117+/-4 to 175+/-5 mm Hg). Muscle workload was increased by stepwise increases in pacing frequency (up to 2 Hz). After increased work, [NADH]m fell and then slowly recovered toward control levels. When work was decreased, [NADH]m overshot control values and then slowly returned. The Ca2+-independent initial fall was larger for trabeculae from rats with hypertrophied hearts than from control rats (eg, 17+/-2% versus 11+/-1% when work was increased by increasing the frequency from 0.25 to 1 Hz). At 1 Hz, average [Ca2+]c was approximately 280 nmol/L, and the Ca2+-dependent [NADH]m recovery was larger for trabeculae from rats with hypertrophied hearts (17+/-4% versus 10+/-2%) despite similar average [Ca2+]c. At steady state after Ca2+-dependent recovery, there was no difference in [NADH]m (fall of 1+/-2% versus 1+/-1%). Furthermore, the Ca2+-dependent overshoot was larger for trabeculae from hypertrophied than from control hearts (increase of 14+/-2% versus 9+/-2% when frequency was decreased from 1 to 0.25 Hz). We conclude that (1) there is initially a larger imbalance in NADH production versus consumption rate in hypertrophy (because NADH fell more) and (2) the Ca2+-dependent recovery mechanism is enhanced in hypertrophy (because NADH recovered and overshot more), thus compensating for the larger imbalance.

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Year:  1998        PMID: 9633918     DOI: 10.1161/01.res.82.11.1189

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  14 in total

1.  Analysis of the mechanisms of mitochondrial NADH regulation in cardiac trabeculae.

Authors:  R Brandes; D M Bers
Journal:  Biophys J       Date:  1999-09       Impact factor: 4.033

2.  Reduced mitochondrial Ca2+ loading and improved functional recovery after ischemia-reperfusion injury in old vs. young guinea pig hearts.

Authors:  Samhita S Rhodes; Amadou K S Camara; James S Heisner; Matthias L Riess; Mohammed Aldakkak; David F Stowe
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3.  Simultaneous measurements of mitochondrial NADH and Ca(2+) during increased work in intact rat heart trabeculae.

Authors:  Rolf Brandes; Donald M Bers
Journal:  Biophys J       Date:  2002-08       Impact factor: 4.033

4.  Functional coupling as a basic mechanism of feedback regulation of cardiac energy metabolism.

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Journal:  Mol Cell Biochem       Date:  2004 Jan-Feb       Impact factor: 3.396

Review 5.  Excitation-contraction coupling and mitochondrial energetics.

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6.  Rapid changes in NADH and flavin autofluorescence in rat cardiac trabeculae reveal large mitochondrial complex II reserve capacity.

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Journal:  J Physiol       Date:  2015-03-13       Impact factor: 5.182

Review 7.  Mitochondrial calcium and the regulation of metabolism in the heart.

Authors:  George S B Williams; Liron Boyman; W Jonathan Lederer
Journal:  J Mol Cell Cardiol       Date:  2014-11-07       Impact factor: 5.000

Review 8.  Role of mitochondrial Ca2+ in the regulation of cellular energetics.

Authors:  Brian Glancy; Robert S Balaban
Journal:  Biochemistry       Date:  2012-03-29       Impact factor: 3.162

9.  NCLX: the mitochondrial sodium calcium exchanger.

Authors:  Liron Boyman; George S B Williams; Daniel Khananshvili; Israel Sekler; W J Lederer
Journal:  J Mol Cell Cardiol       Date:  2013-03-26       Impact factor: 5.000

Review 10.  Anti-anginal and anti-ischemic effects of late sodium current inhibition.

Authors:  Neil J Wimmer; Peter H Stone
Journal:  Cardiovasc Drugs Ther       Date:  2013-02       Impact factor: 3.727

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