|
|
||||||||
Departments of 1 Biology and 2 Pharmacology and Toxicology, Queen's University, Kingston, Ontario, Canada K7L 3N6
We used spontaneously
hypertensive rats to study remodeling of cardiac bioenergetics
associated with changes in blood pressure. Blood pressure was
manipulated with aggressive antihypertensive treatment combining low
dietary salt and the angiotensin-converting enzyme inhibitor enalapril.
Successive cycles of 2 wk on, 2 wk off treatment led to rapid,
reversible changes in left ventricular (LV) mass (30% change in <10
days). Despite changes in LV mass, specific activities of bioenergetic
(cytochrome-c oxidase, citrate synthase, lactate
dehydrogenase) and reactive oxygen species (ROS) (total cellular
superoxide dismutase) enzymes were actively maintained within
relatively narrow ranges regardless of treatment duration, organismal
age, or transmural region. Although enalapril led to parallel declines
in mitochondrial enzyme content and ventricular mass, total ventricular
mtDNA content was unaffected. Altered enzymatic content occurred
without significant changes in relevant mRNA and protein levels.
Transcript levels of gene products involved in mtDNA maintenance
(Tfam), mitochondrial protein degradation (LON protease), fusion (fuzzy
onion homolog), and fission (dynamin-like protein, synaptojanin-2
)
were also unchanged. In contrast, enalapril-mediated ventricular and
mitochondrial remodeling was accompanied by a twofold increase in
specific activity of catalase, an indicator of oxidative stress,
suggesting that rapid cardiac adaptation is accompanied by tight
regulation of mitochondrial enzyme activities and increased ROS production.
hypertension; mitochondria; mitochondrial deoxyribonucleic acid; angiotensin-converting enzyme inhibitor; spontaneously hypertensive rats; cytochrome oxidase; oxidative stress
This article has been cited by other articles:
![]() |
N. G. Abraham, J. Cao, D. Sacerdoti, X. Li, and G. Drummond Heme oxygenase: the key to renal function regulation Am J Physiol Renal Physiol, November 1, 2009; 297(5): F1137 - F1152. [Abstract] [Full Text] [PDF] |
||||
![]() |
M.-C. Battista, E. Calvo, A. Chorvatova, B. Comte, J. Corbeil, and M. Brochu Intra-uterine growth restriction and the programming of left ventricular remodelling in female rats J. Physiol., May 15, 2005; 565(1): 197 - 205. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. C. Dalziel, S. E. Moore, and C. D. Moyes Mitochondrial enzyme content in the muscles of high-performance fish: evolution and variation among fiber types Am J Physiol Regulatory Integrative Comp Physiol, January 1, 2005; 288(1): R163 - R172. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Benderdour, G. Charron, B. Comte, R. Ayoub, D. Beaudry, S. Foisy, D. deBlois, and C. Des Rosiers Decreased cardiac mitochondrial NADP+-isocitrate dehydrogenase activity and expression: a marker of oxidative stress in hypertrophy development Am J Physiol Heart Circ Physiol, November 1, 2004; 287(5): H2122 - H2131. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Bosy-Westphal, C. Eichhorn, D. Kutzner, K. Illner, M. Heller, and M. J. Muller The Age-Related Decline in Resting Energy Expenditure in Humans Is Due to the Loss of Fat-Free Mass and to Alterations in Its Metabolically Active Components J. Nutr., July 1, 2003; 133(7): 2356 - 2362. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |