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. Author manuscript; available in PMC: 2010 Jan 29.
Published in final edited form as: Neuron. 2009 Jan 29;61(2):287–300. doi: 10.1016/j.neuron.2008.12.013

Figure 7. Enhancement of burst firing requires PLC activation, release of Ca2+ from internal stores, and an increase in intracellular Ca2+ concentration.

Figure 7

Layout is as described for Fig. 2.

A. Representative (left) and group (right; n=8) data from experiments in which TBS was given in the presence of a PLC inhibitor (U-73122, 25 μM). B. Representative (left) and group (right) data from experiments in which the internal recording solution contained the Ca2+-ATPase inhibitor thapsigargin (2 μM). In the group data, red circles indicate experiments in which TBS was given (n=6). Group data are also shown for experiments in which no TBS was given (right, black squares; n=6). C. Representative (left) and group (right) data from experiments in which the internal recording solution contained the Ca2+ chelator (BAPTA, 10 mM). In the group data, red circles indicate experiments in which TBS was given (n=5). Group data are also shown for experiments in which no TBS was given (right, black squares; n=5).