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. 2016 Dec 6;174(2):126–138. doi: 10.1111/bph.13661

Figure 7.

Figure 7

Effects of TRP channel antagonists, capsazepine, HC‐030031, M8‐B and BCTC on the activation of high threshold afferents induced by H2O2 and by corresponding agonists. (A) Average data of the effect of capsazepine (10 μM) on H2O2 (300 μM)‐induced activation of high threshold afferents (n = 8, N = 5). (B) Average data of the effects of capsazepine (10 μM) on capsaicin (0.5 μM)‐induced activation of high threshold afferents (n = 10, N = 5). (C) Average data of the effect of HC‐030031 (10 μM) on AITC (30 μM)‐induced activation of high threshold afferents (n = 11, N = 5). (D) Average data of the effect of M8‐B (3 μM) on H2O2 (1 mM)‐induced activation of high threshold afferents (n = 7, N = 5). (E) Average data of the effect of M8‐B (3 μM) on icilin (10 μM)‐induced activation of high threshold afferents (n = 6, N = 5). (F) Average data of the effect of BCTC (10 μM) on H2O2 (1 mM)‐induced activation of high threshold afferents (n = 8, N = 5). *P < 0.05, significant effect of channel antagonist. Note that repeated application of H2O2 (300 μM) on the same capsaicin‐sensitive high threshold afferents without antagonists produced a non‐significant decay in its responses (see Figure 6B).