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Mol Brain
2008 Oct 29;1:14. doi: 10.1186/1756-6606-1-14.
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Development of selective blockers for Ca²(+)-activated Cl channel using Xenopus laevis oocytes with an improved drug screening strategy.
Oh SJ
,
Park JH
,
Han S
,
Lee JK
,
Roh EJ
,
Lee CJ
.
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Ca²(+)-activated Cl⁻ channels (CaCCs) participate in many important physiological processes. However, the lack of effective and selective blockers has hindered the study of these channels, mostly due to the lack of good assay system. Here, we have developed a reliable drug screening method for better blockers of CaCCs, using the endogeneous CaCCs in Xenopus laevis oocytes and two-electrode voltage-clamp (TEVC) technique. Oocytes were prepared with a treatment of Ca²(+) ionophore, which was followed by a treatment of thapsigargin which depletes Ca²(+) stores to eliminate any contribution of Ca²(+) release. TEVC was performed with micropipette containing chelerythrine to prevent PKC dependent run-up or run-down. Under these conditions, Ca²(+)-activated Cl⁻ currents induced by bath application of Ca²(+) to oocytes showed stable peak amplitude when repetitively activated, allowing us to test several concentrations of a test compound from one oocyte. Inhibitory activities of commercially available blockers and synthesized anthranilic acid derivatives were tested using this method. As a result, newly synthesized N-(4-trifluoromethylphenyl)anthranilic acid with trifluoromethyl group (-CF₃) at para position on the benzene ring showed the lowest IC₅₀. Our results provide an optimal drug screening strategy suitable for high throughput screening, and propose N-(4-trifluoromethylphenyl)anthranilic acid as an improved CaCC blocker.
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
Figure 2. Effect of known blockers on Ca2+ activated Cl- channel. (A) Trace of Ca2+ activated Cl- channel current before and during application of flufenamic acid (FA). (B) Dose response relation of flufenamic acid block of Ca2+ activated Cl- current. (C) Summary of IC50s of commercially available blockers for Ca2+-activated Cl- channel. n indicates number of oocytes. Error bars indicate SEMs.
Figure 3. Chemical structures and IC50s of known blockers and anthranilic acid derivatives. (A) Known blockers. (B) Anthranilic acid derivatives; positional compounds. (C) Anthranilic acid derivatives that have variable substituent group on para position of benzene ring. LP: Low Potency. IC50 > 200 μM. n indicates number of oocytes.
Figure 4. Positional effect of substituent group on the phenyl ring of blocker that affects block of Ca2+-activated Cl- current. (A) Comparison of chemical structure, IC50 and dose response between N-(2-nitrophenyl)anthranilic acid, N-(3-nitrophenyl)anthranilic acid and N-(4-nitrophenyl)anthranilic acid in which the nitro (-NO2) group on the benzene ring is positioned at ortho, meta and para position. (B) Comparison of chemical structure, IC50 and dose response between flufenamic acid and derivatives N-(2-trifluoromethylphenyl)anthranilic acid and N-(4-trifluoromethylphenyl)anthranilic acid in which the trifluoromethyl (-CF3) group on the benzene ring is positioned at ortho, meta and para position. Shaded boxes indicate the substituent groups tested. n indicates number of oocytes. Error bars indicate SEMs.
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