Effects of bicarbonate buffered dialysate on human peritoneal mesothelial cell intracellular calcium homeostasis |
| |
Authors: | Bird Stephen D Walker Robert J |
| |
Affiliation: | Department of Medical and Surgical Science, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand |
| |
Abstract: | This study compares the biocompatibility of two bicarbonate-based peritoneal dialysis (PD) solutions using the measurement of intracellular free calcium (Ca(i)2+)) as a sensitive parameter of cell function in human peritoneal mesothelial cells (hPMC). Fura-2-loaded hPMC suspensions were exposed to bicarbonate (38 mmol/L) and bicarbonate (25 mmol/L), lactate-buffered PD (15 mmol/L) solutions at pH 7.4 and compared with Krebs-Ringer physiological saline (KRS; pH = 7.4). Resting Ca(i)2+ values and 4br-A23187 (1.0 micro mol/L) induced transients were compared in treatment and control groups. In separate studies, the effect that low saline pH had on Ca(i)(2+) homeostasis was examined. Suspended cells or cells attached to coverslips were bathed in citric acid-phosphate (McIllvaine's) buffered saline (MBS, pH = 7.4). Cells were acidified (pH = 5.3) with citric acid and then challenged with ionophore. Ionophore challenge produced a significantly reduced Ca(i)2+ transient response in cells exposed to the bicarbonate/lactate fluid compared with bicarbonate or KRS. Acidified cell suspensions produced a small monophasic Ca(i)2+ transient rise that was short lived. Gradual recovery of MBS to pH 7.4 produced no changes to Ca(i)2+ homeostasis of cell monolayers. Ionophore treatment produced a biphasic response identical to cells bathed in KRS. This study has demonstrated that short-term exposure to bicarbonate did not alter Ca(i)2+ homeostasis directly, or subsequent modulation of intracellular pH. The MBS system provided a reliable method of modifying the external pH during continuous Ca(i)2+ measurement. |
| |
Keywords: | bicarbonate buffer intracellular calcium lactate McIlvaine's universal buffer peritoneal dialysis |
本文献已被 PubMed 等数据库收录! |
|