Abstract
Changes in the intracellular concentration of Ca2+ ([Ca2+]in) that occur during prolonged depolarization of the plasma membrane were studied in isolated neurons of the edible snailHelix pomatia, using the calcium-sensitive probe Fura-2. The dependence of the amplitude of the calcium response on the value of the depolarization in the presence of 5 mM caffeine, in contrast to that observed in a normal solution, practically disappeared. This fact indicates that caffeine promotes calcium-dependent release of Ca2+ from the intracellular depots, which is the determining factor in the increase in [Ca2+]in during depolarization. Processes of reduction of [Ca2+]in to the steady-state levels were described by one exponential function, and in the presence of caffeine they occurred twice as rapidly as in the normal solution. Such an acceleration of the kinetics of the relaxation of [Ca2+]in is evidently associated with an increase in the efficiency of the work of the calcium pump of the intracellular calcium depots, which might lead to a decrease in the steady-state of level of [Ca2+]in even below the level observed for the normal extracellular solution.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.