TY - JOUR
T1 - Electrophysiological insights into the relationship between calcium dynamics and cardiomyocyte beating function in chronic hemodialysis treatment
AU - Hamada, Hiroyuki
AU - Tomo, Tadashi
AU - Kim, Sung Teh
AU - Hanai, Taizo
AU - Okamoto, Masahiro
AU - Yamashita, Akihiro C.
N1 - Funding Information:
This research was supported by JSAO Grant MERA 2015 and JSPS KAKENHI Grant Number JP18K12131. We thank Prof. DM. Bers and Prof. D. Sato in the University of California at Davis, and our colleagues from the committee for application of new technologies to blood purification therapy in Japanese Society of Dialysis Therapy who provided insight and expertise that greatly assisted the research.
Funding Information:
Akihiro C. Yamashita has received research funding from Nipro Co., Osaka, Japan, and from Asahi-Kasei Medical Co., Tokyo, Japan, and has advisory role for Nikkiso Co., Tokyo, Japan, and for Asahi-Kasei Medical Co., Tokyo, Japan. Other authors declare that they have no conflict of interest.
Funding Information:
This research was supported by JSAO Grant MERA 2015 and JSPS KAKENHI Grant Number JP18K12131. We thank Prof. DM. Bers and Prof. D. Sato in the University of California at Davis, and our colleagues from the committee for application of new technologies to blood purification therapy in Japanese Society of Dialysis Therapy who provided insight and expertise that greatly assisted the research.
Publisher Copyright:
© 2020, The Japanese Society for Artificial Organs.
PY - 2021/3
Y1 - 2021/3
N2 - For patients in which the Ca2+ concentration of dialysis fluid is lower than that in plasma, chronic hemodialysis treatment often leads to cardiac beating dysfunction. By applying these conditions to an electrophysiological mathematical model, we evaluated the impact of body fluid Ca2+ dynamics during treatment on cardiomyocyte beating and, moreover, explored measures that may prevent cardiomyocyte beating dysfunction. First, Ca2+ concentrations in both plasma and interstitial fluid were decreased with treatment time, which induced both a slight decline in beating rhythm on a sinoatrial nodal cell and a wane in contraction force on a ventricular cell. These simulated results were in agreement with clinical observations. Next, a relationship between the intracellular Ca2+ concentration and ion current dynamics of ion transporters were examined to elucidate the mechanism underlying cardiomyocyte beating dysfunction. The inward current of the Na/Ca exchanger (NCX) increased with a decrease in Ca2+ concentration in interstitial fluid and induced a reduction in intracellular Ca2+ concentration during treatment. Furthermore, the decline in intracellular Ca2+ concentration reduced the contraction force. These findings implied that ion transport through the NCX is a dominant factor that induces cardiomyocyte beating dysfunction during hemodialysis. Finally, the replenishment of Ca2+ or application of an NCX inhibitor during treatment suppressed the decrease in intracellular Ca2+ concentration and contributed to the stabilization of cardiomyocyte beating function. In summary, the clinical implementation of hepatically cleared NCX inhibitor may be a suitable approach to improving the quality of life for patients on chronic hemodialysis.
AB - For patients in which the Ca2+ concentration of dialysis fluid is lower than that in plasma, chronic hemodialysis treatment often leads to cardiac beating dysfunction. By applying these conditions to an electrophysiological mathematical model, we evaluated the impact of body fluid Ca2+ dynamics during treatment on cardiomyocyte beating and, moreover, explored measures that may prevent cardiomyocyte beating dysfunction. First, Ca2+ concentrations in both plasma and interstitial fluid were decreased with treatment time, which induced both a slight decline in beating rhythm on a sinoatrial nodal cell and a wane in contraction force on a ventricular cell. These simulated results were in agreement with clinical observations. Next, a relationship between the intracellular Ca2+ concentration and ion current dynamics of ion transporters were examined to elucidate the mechanism underlying cardiomyocyte beating dysfunction. The inward current of the Na/Ca exchanger (NCX) increased with a decrease in Ca2+ concentration in interstitial fluid and induced a reduction in intracellular Ca2+ concentration during treatment. Furthermore, the decline in intracellular Ca2+ concentration reduced the contraction force. These findings implied that ion transport through the NCX is a dominant factor that induces cardiomyocyte beating dysfunction during hemodialysis. Finally, the replenishment of Ca2+ or application of an NCX inhibitor during treatment suppressed the decrease in intracellular Ca2+ concentration and contributed to the stabilization of cardiomyocyte beating function. In summary, the clinical implementation of hepatically cleared NCX inhibitor may be a suitable approach to improving the quality of life for patients on chronic hemodialysis.
UR - http://www.scopus.com/inward/record.url?scp=85090757387&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85090757387&partnerID=8YFLogxK
U2 - 10.1007/s10047-020-01207-7
DO - 10.1007/s10047-020-01207-7
M3 - Article
C2 - 32910365
AN - SCOPUS:85090757387
SN - 1434-7229
VL - 24
SP - 58
EP - 64
JO - Journal of Artificial Organs
JF - Journal of Artificial Organs
IS - 1
ER -