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Fig. 5. Effects of withdrawal of extracellular Ca2+ on the rate of decline of STOCs and on the response to InsP3. Depolarisation to -10 mV from a holding potential of -70 mV (iii) induced STOCs (i) and raised [Ca2+]i (ii). Removal of extracellular Ca2+ for the duration indicated by the bar abolished STOCs and lowered [Ca2+]i to pre-depolarisation levels. The times on the bars indicate the period in Ca2+-free/1mM EGTA solution prior to the release of InsP3 (ii). A 4 minute period separated the traces as indicated by the gap. At -10 mV the responses to InsP3 ({uparrow}, iii) were elicited 0.5, 1, 2, 4 and 8 minutes after Ca2+ withdrawal and compared with control responses to InsP3 obtained before removal of extracellular Ca2+. Ca2+ withdrawal reduced the amplitude of both STOCs and the InsP3 responses, the rate of decline of the former exceeded that of the latter (iv). These results suggest that the Ca2+ store content required to support STOCs is greater that that to maintain InsP3 responses.





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