Angiotensin II–Induced Growth Responses in Isolated Adult Rat Hearts

1995 ◽  
Vol 76 (3) ◽  
pp. 489-497 ◽  
Author(s):  
Heribert Schunkert ◽  
Jun-ichi Sadoshima ◽  
Torsten Cornelius ◽  
Yutaka Kagaya ◽  
Ellen O. Weinberg ◽  
...  
Circulation ◽  
1997 ◽  
Vol 95 (12) ◽  
pp. 2677-2683 ◽  
Author(s):  
Christiane D. Thienelt ◽  
Ellen O. Weinberg ◽  
Jozef Bartunek ◽  
Beverly H. Lorell

Author(s):  
Takashi Haneda ◽  
Jun Fukuzawa ◽  
Setsuya Miyata ◽  
Junzo Osaki ◽  
Yasuhiro Nakamura ◽  
...  

1996 ◽  
Vol 27 (2) ◽  
pp. 31-32
Author(s):  
Kazuhide Ogino ◽  
Bolin Cai ◽  
Takushi Kohmoto ◽  
Guven Uzun ◽  
Milton Packer ◽  
...  

1996 ◽  
Vol 63 (1) ◽  
pp. 9-16 ◽  
Author(s):  
Natacha R. Bastien ◽  
Gladys M. Ciuffo ◽  
Juan M. Saavedra ◽  
Chantal Lambert

2001 ◽  
Vol 19 (6) ◽  
pp. 1121-1129 ◽  
Author(s):  
Rohit Moudgil ◽  
Vijayan Menon ◽  
Yi Xu ◽  
Sorin Musat-Marcu ◽  
Dinender Kumar ◽  
...  

2011 ◽  
Vol 301 (1) ◽  
pp. H180-H191 ◽  
Author(s):  
Norishige Morita ◽  
Jong-Hwan Lee ◽  
Aneesh Bapat ◽  
Michael C. Fishbein ◽  
William J. Mandel ◽  
...  

Selective glycolytic inhibition (GI) promotes electromechanical alternans and triggered beats in isolated cardiac myocytes. We sought to determine whether GI promotes triggered activity by early afterdepolarization (EAD) or delayed afterdepolarizations in intact hearts isolated from adult and aged rats. Dual voltage and intracellular calcium ion (Cai2+) fluorescent optical maps and single cell glass microelectrode recordings were made from the left ventricular (LV) epicardium of isolated Langendorff-perfused adult (∼4 mo) and aged (∼24 mo) rat hearts. GI was induced by replacing glucose with 10 mM pyruvate in oxygenated Tyrode's. Within 20 min, GI slowed Cai2+ transient decline rate and shortened action potential duration in both groups. These changes were associated with ventricular fibrillation (VF) in the aged hearts (64 out of 66) but not in adult hearts (0 out of 18; P < 0.001). VF was preceded by a transient period of focal ventricular tachycardia caused by EAD-mediated triggered activity leading to VF within seconds. The VF was suppressed by the ATP-sensitive K (KATP) channel blocker glibenclamide (1 μM) but not (0 out of 7) by mitochondrial KATP block. The Ca-calmodulin-dependent protein kinase II (CaMKII) blocker KN-93 (1 μM) prevented GI-mediated VF ( P < 0.05). Block of Na-Ca exchanger (NCX) by SEA0400 (2 μM) prevented GI-mediated VF (3 out of 6), provided significant bradycardia did not occur. Aged hearts had significantly greater LV fibrosis and reduced connexin 43 than adult hearts ( P < 0.05). We conclude that in aged fibrotic unlike in adult rat hearts, GI promotes EADs, triggered activity, and VF by activation of KATP channels CaMKII and NCX.


1999 ◽  
Vol 40 (4) ◽  
pp. 461-469 ◽  
Author(s):  
Tatsuya NUNOHIRO ◽  
Naoto ASHIZAWA ◽  
Kristof GRAF ◽  
Willa HSUEH ◽  
Katsusuke YANO

2008 ◽  
Vol 295 (2) ◽  
pp. H647-H656 ◽  
Author(s):  
Chao Yuan ◽  
Quanhu Sheng ◽  
Haixu Tang ◽  
Yixue Li ◽  
Rong Zeng ◽  
...  

Neonatal hearts respond to stress and function in an environment quite different from adult hearts. There is evidence that these functional differences not only reflect modifications in the abundance and isoforms of sarcomeric proteins but also in the modulation of sarcomeric protein phosphorylation. Yet our understanding of changes in sarcomeric protein phosphorylation in development is incomplete. In the experiments reported here, we first quantified the intact sarcomeric protein phosphorylation status between neonatal and adult rat hearts by employing comparative two-dimensional (2-D) gel electrophoresis in conjunction with phosphoprotein-specific staining. Subsequently, we measured phosphorylation changes at the peptide level by employing high-resolution linear ion trap-Fourier transform (LTQ-FT) mass spectrometry analysis of titanium dioxide-enriched phosphopeptides differentially labeled with 16O/18O during in-gel digestion. We also employed Western blot analysis using phosphorylation site-specific antibodies to measure phosphorylation changes. Our data demonstrated the novel finding that phosphorylation levels of myosin-binding protein C (MyBP-C) at Ser295 and Ser315 as well as tropomyosin at Ser283 increased, whereas phosphorylation levels of MyBP-C at Ser320 and myosin light chain 2 at Ser15 decreased in neonatal hearts compared with the same sites in adult hearts. Although our data highlight the significant challenges in understanding relations between protein phosphorylation and cardiac function, they do support the hypothesis that developmental changes in the modulation of protein are functionally significant and correlate with the prevailing physiological state.


1983 ◽  
Vol 219 (1217) ◽  
pp. 447-469 ◽  

The second inward current ( I si ) in single cells isolated from ventricular muscle of adult rat hearts was measured in response to step depolarizations under voltage-clamp conditions. The major ion carrying this current was Ca, and I si was reduced or abolished by Mn, Ni, Cd, nifedipine, nimodipine and D600. Sr and Ba could substitute for Ca as charge carriers, and reduced the rate of apparent inactivation of I si . These effects of Sr and Ba, together with the relation between the steady level of apparent inactivation and membrane potential in Ca containing solution, were taken as evidence that inactivation was at least in part dependent on internal Ca. The reduction of external Na to 11% of normal caused a reduction in peak I si when Ca was present in the external solution, but did not reduce I si when Ca was replaced by Sr. It therefore seems unlikely that Na is a major charge carrier I si under the conditions of our experiments. The time-to-peak and rate of apparent inactivation of I si were faster than in previous studies that used multicellular preparations. Both the kinetics and peak amplitude of I si were markedly dependent on temperature ( Q 10 close to 3). Contraction of the cells, which was monitored optically, was initiated within 3 ms of the peak I si , reached a maximum level after approximately 40–50 ms, and was about 100 ms in duration.


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