Skip to main content
Figure 1 | Molecular Brain

Figure 1

From: Development of selective blockers for Ca2+-activated Cl- channel using Xenopus laevis oocytes with an improved drug screening strategy

Figure 1

Endogeneous Ca2+ activated Cl- channels in Xenopus laevis oocyte. (A) Currents induced by extracellular Ca2+ in a dose dependent manner on ionomycin treated oocyte. (B) Dose response and EC50 of Ca2+ obtained from (A). (C~F) Currents recorded after treatment of ionomycin without thapsigargin treatment. (C, G) Fast peak and slow component during Ca2+ applications. (G~J) Currents recorded after treatment of ionomycin followed by thapsigargin. (D, H) Second application of Ca2+ induces slightly reduced fast peak amplitude compared to the first peak. (E, I) Ba2+ does not induce the slow component. (F, J) Ba2+ does not induce the fast peak. (K~O) Comparison of currents under each condition. CHE+ means that current was measured with chelerythrine added intracellular solution. TG+ indicates that thapsigargin was treated on ionomycin pretreated oocytes. (K) Fast peak amplitude. (L) Slow component amplitude. (M) Summary of the experiments shown in (D) and (H); Ratio of amplitude induced by the first and the second Ca2+. (N) Summary of the experiments shown in (E) and (I). (O) Summary of the experiments shown in (F) and (J). n indicates number of oocytes. Error bars indicate SEMs. * indicates statistically significant difference by two-tailed t-test. *, p < 0.05; **, p < 0.01; ***, p < 0.001

Back to article page