Abstract
Understanding developmental changes in contractility is critical to improving therapies for young cardiac patients. Isometric developed force was measured in human ventricular muscle strips from two age groups: newborns (<2 wk) and infants (3–14 mo) undergoing repair for congenital heart defects. Muscle strips were paced at several cycle lengths (CLs) to determine the force frequency response (FFR). Changes in Na/Ca exchanger (NCX), sarcoplasmic reticulum Ca-ATPase (SERCA), and phospholamban (PLB) were characterized. At CL 2000 ms, developed force was similar in the two groups. Decreasing CL increased developed force in the infant group to 131 ± 8% (CL 1000 ms) and 157 ± 18% (CL 500 ms) demonstrating a positive FFR. The FFR in the newborn group was flat. NCX mRNA and protein levels were significantly larger in the newborn than infant group whereas SERCA levels were unchanged. PLB mRNA levels and PLB/SERCA ratio increased with age. Immunostaining for NCX in isolated newborn cells showed peripheral staining. In infant cells, NCX was also found in T-tubules. SERCA staining was regular and striated in both groups. This study shows for the first time that the newborn human ventricle has a flat FFR, which increases with age and may be caused by developmental changes in calcium handling.
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Abbreviations
- CamKII:
-
calcium/calmodulin-dependent kinase II
- CL:
-
cycle length
- FDAR:
-
frequency dependent acceleration of relaxation
- FFR:
-
force frequency relationship
- HLHS:
-
hypoplastic left heart syndrome
- NCX:
-
Na/Ca exchanger
- PLB:
-
phospholamban
- SERCA:
-
SR calcium-ATPase
- SR:
-
sarcoplasmic reticulum
- TOF:
-
tetralogy of Fallot
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Supported by Grants HL-088488 (M.B.W.) and HL-077485 (R.W.J.) from the National Heart, Lung and Blood Institute, by Grant in Aid 0755537B (M.B.W.) from the American Heart Association Southeast Affiliate, and by financial support from Children's Healthcare of Atlanta.
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Wiegerinck, R., Cojoc, A., Zeidenweber, C. et al. Force Frequency Relationship of the Human Ventricle Increases During Early Postnatal Development. Pediatr Res 65, 414–419 (2009). https://doi.org/10.1203/PDR.0b013e318199093c
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DOI: https://doi.org/10.1203/PDR.0b013e318199093c
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