Hyponatraemia alters the biophysical properties of neuronal cells independently of osmolarity: a study on Ni2+‐sensitive current involvement

• Published in: Experimental physiology 2016-08, Vol.101 (8), p.1086-1100
• Main Authors: Squecco, Roberta, Luciani, Paola, Idrizaj, Eglantina, Deledda, Cristiana, Benvenuti, Susanna, Giuliani, Corinna, Fibbi, Benedetta, Peri, Alessandro, Francini, Fabio
• Format: Article
• Language: English
• ISSN: 0958-0670; 1469-445X
• DOI: 10.1113/EP085806

New Findings What is the central question of this study? Hyponatraemia, an electrolyte disorder encountered in hospitalized patients, can cause neurological symptoms usually attributed to a reduction in plasma osmolarity. Here, we investigated whether low [Na+] per se can cause neuronal changes independent of osmolarity, focusing on involvement of the Na+–Ca2+ exchanger. What is the main finding and its importance? We show that hyponatraemia per se causes alterations of neuronal properties. The novel finding of Na+–Ca2+ exchanger involvement helps us to elucidate the volume regulation following hyponatraemia. This might have relevance in a translational perspective because Na+–Ca2+ exchanger could be a target for novel therapies. Hyponatraemia is the most frequent electrolyte disorder encountered in hospitalized patients, and it can cause a wide variety of neurological symptoms. Most of the negative effects of this condition on neuronal cells are attributed to cell swelling because of the reduction of plasma osmolarity, although in hyponatraemia different membrane proteins are supposed to be involved in the conservation of neuronal volume. We have recently reported detrimental effects of hyponatraemia on two different neuronal cell lines, SK‐N‐AS and SH‐SY5Y, independent of osmotic alterations. In this study we investigated, in the same cell lines, whether hyponatraemic conditions per se can cause electrophysiological alterations and whether these effects vary over time. Accordingly, we carried out experiments in low‐sodium medium in either hyposmotic [Osm(−)] or isosmotic [Osm(+)] conditions, for a short (24 h) or long time (7 days). Using a patch pipette in voltage‐clamp conditions, we recorded possible modifications of cell capacitance (Cm) and membrane conductance (Gm). Our results indicate that in both Osm(−) and Osm(+) medium, Cm and Gm show a similar increase, but such effects are dependent on the time in culture in different ways. Notably, regarding the possible mechanisms involved in the maintenance of Cm, Gm and Gm/Cm in Osm(+) conditions, we observed a greater contribution of the Na+–Ca2+ exchanger compared with Osm(−) and control conditions. Overall, these novel electrophysiological results help us to understand the mechanisms of volume regulation after ionic perturbation. Our results might also have relevance in a translational perspective because the Na+–Ca2+ exchanger can be considered a target for planning novel therapies.