Faculty Opinions recommendation of Decreased cardiac L-type Ca²⁺ channel activity induces hypertrophy and heart failure in mice.

Author(s):  
Céline Fiset
1993 ◽  
Vol 264 (3) ◽  
pp. H926-H937 ◽  
Author(s):  
C. R. Cory ◽  
L. J. McCutcheon ◽  
M. O'Grady ◽  
A. W. Pang ◽  
J. D. Geiger ◽  
...  

In this study we tested the hypothesis that the ryanodine-binding Ca-release channel activity and density of the sarcoplasmic reticulum (SR) terminal cisternae were decreased in congestive heart failure (CHF) that occurs spontaneously in doberman pinschers or experimentally with rapid ventricular pacing of mongrels. We used a novel, sensitive, and easy-to-perform microassay and demonstrated a 50% decrease in activity of the myocardial SR Ca pump and a 75% reduction in SR Ca-release channel activity in CHF. Decreases in Ca channel content were associated with increases in net Ca sequestration. 45Ca-release experiments from passively loaded SR terminal cisternae and ryanodine-binding studies confirmed a 53–68% downregulation of the Ca-release channel activity. As a consequence of release channel downregulation, there was partial restoration of net Ca sequestration activity in dogs with CHF and complete compensation in dogs with mild cardiac dysfunction. Deterioration of Ca cycling correlated with deterioration of myocardial performance, apparently due to decreased Ca-adenosinetriphosphatase (ATPase) pump and not Ca channel content. One-half the reduction in Ca-release activity could be attributed to decreased Ca sequestration and one-half to decreased Ca channel density. Downregulation of Ca channel content decreases the amplitude of the Ca cycle and maximizes the downregulation of Ca pumps that may occur. Although these adaptations may reduce cellular energy expenditure, they are likely to render the myocardium more susceptible to fatigue and failure.


1994 ◽  
Vol 72 (9) ◽  
pp. 999-1006 ◽  
Author(s):  
Peter James O'Brien ◽  
Gordon W. Moe ◽  
Linda M. Nowack ◽  
Etienne A. Grima ◽  
Paul W. Armstrong

The contraction–relaxation cycle of the heart is dependent on a cycle of ATP production and utilization and a cycle of Ca uptake and Ca release by the sarcoplasmic reticulum (SR). Heart failure (HF) is associated with abnormalities of myocardial Ca and ATP cycling, but the time course of their development is unknown. This study tested the hypothesis that, compared with ATP-utilizing and Ca-uptake activities, decreases in ATP-synthesis and Ca-release activities occurred earlier in the development of HF and persisted longer during recovery from HF. HF was induced by right ventricular pacing of dogs at 250 beats/min. Dogs were studied after 1 week of pacing (n = 8, early HF), at HF (n = 11, severe HF), and 4 weeks after cessation of pacing (n = 9) and were compared with dogs not subjected to pacing. At early HF, there were decreased activities (p < 0.05) of the SR Ca-release channel (rate constant from 199 ± 36 × 10−4 to 90 ± 16 × 10−4 s−1), mitochondrial ATP synthesis (from 11.2 ± 2.4 to 7.0 ± 2.2 international units (IU)/g), and creatine kinase (CK) from 2028 ± 266 to 1811 ± 79 IU/g). The decreased Ca-channel activity was due to a 32% decrease in maximal activity (rate constant from 249 ± 50 × 10−4 to 170 ± 29 × 10−4 s−1) and to a 2-fold increase (from 19.1 ± 12.4 to 42.0 ± 14.2%) in inhibition of maximal channel activity (p < 0.05). At severe HF, Ca-uptake (rate constant from 407 ± 41 × 10−4 to 296 ± 77 × 10−4 s−1) and ATP-utilization activities also became depressed (from 27.2 ± 3.3 to 20.3 ± 1.9 IU/g), and CK further decreased to 1321 ± 241 IU/g (p < 0.05). Four weeks after cessation of pacing, only total Ca-cycling (sum of Ca uptake and Ca release), Ca-uptake, and CK activities were significantly recovered (p < 0.05). Left ventricular ejection fraction was significantly correlated with total Ca cycling (n = 12, r = 0.68, p < 0.02), Ca-channel inhibition (n = 12, r = −0.60, p < 0.04), and basal ATPase (n = 11, r = 0.69, p < 0.02). We conclude that biochemical measurements of ATP- and Ca-cycling activities correlate with myocardial performance, and that compared with ATP-utilization and Ca-uptake activities, inhibition of ATP synthesis and Ca release occurs earlier in the development of HF and persists longer during recovery from HF.Key words: Ca-release channel, sarcoplasmic reticulum, rapid ventricular pacing, congestive heart failure, Ca ATPase pump, mitochondria.


2012 ◽  
Vol 302 (8) ◽  
pp. H1645-H1654 ◽  
Author(s):  
Toshihide Kashihara ◽  
Tsutomu Nakada ◽  
Hisashi Shimojo ◽  
Miwa Horiuchi-Hirose ◽  
Simmon Gomi ◽  
...  

L-type Ca2+ channels (LTCCs) play an essential role in the excitation-contraction coupling of ventricular myocytes. We previously found that t-tubular (TT) LTCC current density was halved by the activation of protein phosphatase (PP)1 and/or PP2A, whereas surface sarcolemmal (SS) LTCC current density was increased by the inhibition of PP1 and/or PP2A activity in failing ventricular myocytes of mice chronically treated with isoproterenol (ISO mice). In the present study, we examined the possible involvement of inhibitory heterotrimeric G proteins (Gi/o) in these abnormalities by chronically administrating pertussis toxin (PTX) to ISO mice (ISO + PTX mice). Compared with ISO mice, ISO + PTX mice exhibited significantly higher fractional shortening of the left ventricle. The expression level of Gαi2 proteins was not altered by the treatment of mice with ISO and/or PTX. ISO + PTX myocytes had normal TT and SS LTCC current densities because they had higher and lower availability and/or open probability of TT and SS LTCCs than ISO myocytes, respectively. A selective PKA inhibitor, H-89, did not affect LTCC current densities in ISO + PTX myocytes. A selective PP2A inhibitor, fostriecin, did not affect SS or TT current density in control or ISO + PTX myocytes but significantly increased TT but not SS LTCC current density in ISO myocytes. These results indicate that chronic receptor-mediated activation of Gi/o in vivo decreases basal TT LTCC activity by activating PP2A and increases basal SS LTCC activity by inhibiting PP1 without modulating PKA in heart failure.


2007 ◽  
Vol 13 (6) ◽  
pp. S30
Author(s):  
Hideyuki Kinoshita ◽  
Koichiro Kuwahara ◽  
Masaki Harada ◽  
Yasuaki Nakagawa ◽  
Michio Nakanishi ◽  
...  

1984 ◽  
Vol 45 (1) ◽  
pp. 130-132 ◽  
Author(s):  
Nobuyuki Haga ◽  
Michael Forte ◽  
Rajeev Ramanathan ◽  
Yoshiro Saimi ◽  
Mihoko Takahashi ◽  
...  

Physiology ◽  
1991 ◽  
Vol 6 (6) ◽  
pp. 277-281 ◽  
Author(s):  
P Lory ◽  
G Varadi ◽  
A Schwartz

The diversity of voltage-dependent Ca channels is well documented. How excitable cells produce their specific Ca channel activity is being approached by structure-function studies. The implications of multiple gene products, splice variants, and subunit assembly in Ca channel function are updated in this review.


1991 ◽  
Vol 69 (12) ◽  
pp. 1833-1840 ◽  
Author(s):  
Peter James O'Brien ◽  
Hua Shen ◽  
Janice E. Weiler ◽  
S. Mehdi Mirsalimi ◽  
Richard J. Julian

We have previously demonstrated that in furazolidone-induced congestive heart failure in turkeys the specific Ca2+-ATPase activity of myocardial sarcoplasmic reticulum (SR) is 60% increased in compensation for a 50% depression in net Ca2+-sequestration activity. This study tested the hypothesis that SR Ca2+-uptake and Ca2+-ATPase activities were uncoupled in this cardiomyopathy because of increased Ca2+-release channel activity. A novel microassay was used to monitor Ca2+ transport by myocardial homogenates using the fluorescent Ca2+ dye indo 1 to indicate extravesicular ionized Ca2+. The method is applied to cyropreserved biopsy specimens of myocardium and requires only 50 mg tissue. Both SR Ca2+-pump and SR Ca2+-channel activity were estimated using the channel-inhibitor ruthenium red (RR) and the mitochondrial inhibitor sodium azide. The specificity of the RR inhibition was confirmed using ryanodine. Cardiomyopathy was induced in 2-week-old turkey pouits by the addition of 0.07% furazolidone to their feed for 4 weeks. Compared with controls, myocardial maximal Ca2+-channel activity relative to maximal Ca2+-pump activity was 22% greater and duration of Ca2+-channel activity was 100% increased. However, the heart failure birds had 43 and 53% decreases in absolute maximal Ca2+-pumping and Ca2+-channel activities, respectively. The abnormal Ca2+-channel activity resulted in 200% greater time before initiation of net Ca2+ sequestration and 700% greater final myocardial Ca2+ concentrations. For all birds, the Ca2+-accumulating activity was highly correlated with Ca2+-release activity (all p < 0.05). These data indicate that in this animal model of congestive heart failure there is defective SR Ca2+-channel function resulting in abnormal Ca2+ homeostasis. However, this defect can only partially explain our previous finding of furazolidone-induced uncoupling of Ca2+ uptake from Ca2+-ATPase activities. The consequent myocardial Ca2+ overload predisposes the heart to fatigue and irreversible failure.Key words: sarcoplasmic reticulum, calcium sequestration, furazolidone cardiomyopathy, indo 1 spectrofluorometry.


Sign in / Sign up

Export Citation Format

Share Document