Fig. 2. Responses to capsaicin (CAP) and fentanyl in three different sensory neurons. The cell in A  was sensitive to both CAP and fentanyl; the cell in B  was sensitive to CAP but not to fentanyl; the cell in C  was sensitive to neither CAP nor fentanyl. The top panels show inward currents induced by CAP (10 μm; time of CAP application denoted by bar above each trace). The middle panels show representative high-voltage–activated Ca2+current (ICa) traces, and the bottom panels show the Ca2+current–voltage (I-V) relations, before (open squares), during (filled circles), and after (open triangles) washout of fentanyl. Fentanyl concentrations were 100 nm in A  and B  and 1 μm in C . For the CAP-induced current traces, the horizontal scale bars denote 1 s, and the vertical scale bars denote 1 nA. For ICatraces, the horizontal scale bars denote 10 ms, and the vertical scale bars denote 500 pA.

Fig. 2. Responses to capsaicin (CAP) and fentanyl in three different sensory neurons. The cell in A  was sensitive to both CAP and fentanyl; the cell in B  was sensitive to CAP but not to fentanyl; the cell in C  was sensitive to neither CAP nor fentanyl. The top panels show inward currents induced by CAP (10 μm; time of CAP application denoted by bar above each trace). The middle panels show representative high-voltage–activated Ca2+current (ICa) traces, and the bottom panels show the Ca2+current–voltage (I-V) relations, before (open squares), during (filled circles), and after (open triangles) washout of fentanyl. Fentanyl concentrations were 100 nm in A  and B  and 1 μm in C . For the CAP-induced current traces, the horizontal scale bars denote 1 s, and the vertical scale bars denote 1 nA. For ICatraces, the horizontal scale bars denote 10 ms, and the vertical scale bars denote 500 pA.

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