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. 1997 May 15;17(10):3538–3553. doi: 10.1523/JNEUROSCI.17-10-03538.1997

Fig. 8.

Fig. 8.

Protection by BAPTA-AM is attributable to intracellular Ca2+ chelation, not to extracellular Ca2+ buffering or to the AM moiety. Slice cultures were challenged with 60 min OGD in the presence of DMSO alone (DMSO; 24 slices), BAPTA-AM (38 slices), BAPTA tetrapotassium salt (K-BAPTA; 5 slices), which is cell-impermeant, and dinitro-BAPTA-AM (DN-BAPTA-AM; 8 slices), which has a negligible affinity for Ca2+.Asterisks indicate differences from DMSO groups (ANOVA followed by Newman–Keuls procedure for multiple comparisons).