Influence of NO and [Ca2+]o on [Ca2+]i homeostasis in rat ventricular cardiomyocytes. Issue 5 (3rd September 2018)

• Record Type: Journal Article
• Authors: Mitrokhin, Vadim; Mladenov, Mitko; Gorbacheva, Lyubov; Babkina, Irina; Lovchikova, Irina; Kazanski, Viktor; Kamkin, Andre
• Is Part Of: Biotechnology, biotechnological equipment. Volume 32:Issue 5(2018)
• Page Start: 1338
• Page End: 1343
• Publication Date: 2018-09-03
• Subjects: L-type Ca2+ channels -- nitric oxide -- z-disk -- phalloidin -- cardiomyocytes -- rat; Biotechnology -- Periodicals; Biotechnology -- Periodicals; Biotechnology -- instrumentation -- Periodicals; Periodicals; 660.605
• DOI: 10.1080/13102818.2018.1488621
• Languages: English
• ISSNs: 1310-2818

Abstract

Abstract: In this study, we explored the effect of NO-induced changes in [Ca 2+ ]i homeostasis in rat ventricular cardiomyocytes through variation in extracellular Ca 2+ and application of SNAP ( S- nitroso- N -acetyl-d, l -penicillamine) as an NO-donor. The Fura-2 signal dynamics and phalloidin intensity profile of z-disks in rat cardiomyocytes served as endpoints to describe the mechanisms involved in the control of the intracellular Ca 2+ levels, depending on the kinetics of distribution of the SNAP-produced NO. The results demonstrated that SNAP caused small phalloidin intensity profile changes between the z-lines in the presence of [Ca 2+ ]o . However, in the absence of [Ca 2+ ]o, SNAP in a concentration of 300 μmol/L induced a significant decrease in the distance between z-lines. This SNAP-induced decrease was reflected as a decrease in the phalloidin fluorescence intensity in the middle of the sarcomere, due to the preferential imaging of greater fluorescence in the bulk of the thin filaments. Based on the Ca 2+ fluorescence intensity profile, we could suggest that intracellular Ca 2+ is mainly affected by the mechanisms of Ca 2+ outflow, rather than the mechanisms of Ca 2+ inflow in the presence of NO. Actually, through variation in the electrochemical gradient of Ca 2+, we induced mechanisms of faster/slower cytosolic Ca 2+ emptying. The obtained data showed that the delay in the cytosolic Ca 2+ emptying in the presence of [Ca 2+ ]o is due to the increased electrochemical gradient of Ca 2+ .