Dynamic regulation of sodium/calcium exchange function in human heart failure.

, , , and . Circulation 108 (18): 2224--2229 (November 2003)


BACKGROUND: Sarcolemmal Na/Ca exchange (NCX) regulates cardiac Ca and contractility. NCX function during the cardiac cycle is determined by intracellular Ca and Na (Cai, and Nai) and membrane potential (Em), which all change in human heart failure (HF). Therefore, changes in NCX function may contribute to abnormal Ca regulation in human HF. METHODS AND RESULTS: We assessed the cellular bases of differences in NCX function in ventricular myocytes from failing (F) and nonfailing (NF) human hearts. Allosteric activation of NCX by Cai was comparable in F and NF myocytes (K1/2=150+/-31 nmol/L, n=7). The steady-state relation between Cai and NCX current (INCX) was used to infer the local submembrane Cai (Casm) that is sensed by NCX dynamically during the action potential (AP) and Ca transient (37 degrees C). This involved "tail" INCX measurement during abrupt repolarization of APs and Ca transients, where peak inward INCX indicates Casm. This allows inference of the direction of Ca transport by the NCX during the AP. In NF myocytes, NCX extrudes Ca for most of the AP. Three factors shift the direction of NCX-mediated Ca transport (to favor more Ca influx) in F versus NF myocytes, as follows: (1) reduced Casm, (2) prolonged AP duration, and (3) elevated Nai. CONCLUSIONS: These results show that Ca entry through NCX may limit systolic dysfunction due to reduced sarcoplasmic reticulum Ca stores in HF but could contribute to slow decay of the Cai transient and to diastolic dysfunction.


The whole bibliography file I use.

Links and resources

BibTeX key:
search on:

Comments and Reviews  

There is no review or comment yet. You can write one!


Cite this publication