Abnormal calcium re-uptake in myocardium sarcoplasmic reticulum in rabbits with heart failure and the influencing factors.
- Author:
Lei WANG
1
,
2
,
3
;
Shi-Jie ZHANG
;
Li LI
;
Chao LAN
;
Rui ZHANG
;
Zhi-Hua LIU
Author Information
1. Department of Emergency
2. Department of Clinical Laboratory, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China
3. Department of Cardiology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China. zsj03@zzu.edu.cn.
- Publication Type:Journal Article
- MeSH:
Animals;
Calcium;
metabolism;
Calcium-Binding Proteins;
metabolism;
Heart Failure;
physiopathology;
Myocardium;
metabolism;
Phosphorylation;
Rabbits;
Sarcoplasmic Reticulum;
pathology
- From:
Acta Physiologica Sinica
2014;66(4):483-488
- CountryChina
- Language:Chinese
-
Abstract:
The aim of the present study was to investigate the abnormal calcium re-uptake function of myocardium sarcoplasmic reticulum (SR) in rabbits with heart failure, as well as potential mechanisms. Heart failure model was established in rabbits through aortic insufficiency and constriction of abdominal aorta. The SR Ca(2+) re-uptake function was measured with a calcium imaging device. The activity of myocardium SR calcium adenodine triphosphatase 2a (SERCA2a) was measured by inorganic phosphate. The protein expressions of SERCA2a, CaMKII, PKA, PP1α, phospholamban (PLB), PLB-Ser(16) and PLB-Thr(17) were evaluated by Western blot. The activities of PKA and CaMKII were detected by γ-(32)P substrate incorporation. The results showed that, compared with the sham operation group, the heart failure group exhibited reduced Ca(2+) re-uptake amount (P < 0.01) and the expression and activity of SERCA2a (P < 0.05 or P < 0.01), decreased expression of PLB and its phosphorylation status in sites of Ser(16) and Thr(17) (P < 0.05), increased expressions and activities of PKA and CaMKII (P < 0.05 or P < 0.01), and increased expression of PP1α (P < 0.05). These results suggest that the abnormal Ca(2+) re-uptake function in heart failure is related with reduced expression and activities of SERCA2a, as well as reduced expression of PLB and its phosphorylation status. Both PLB-Ser(16) and -Thr(17) may be involved in the regulation of myocardium SR calcium pump activity in heart failure.
