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. 2014 Feb 3;592(Pt 7):1619–1636. doi: 10.1113/jphysiol.2013.262782

Figure 5.

Figure 5

All light stimuli were 8.5 log quanta cm−2 s−1, below the threshold intensity for inducing melanopsin responses. In the top traces, to analyse amacrine-driven light responses in isolation, ipRGCs were voltage clamped at the reversal potential for cationic input (Ecations). The arrows highlight light-off conductance increases detected in M1 and M3 cells, the only ipRGC types that possess dendrites in the ‘off’ sublamina of the inner plexiform layer. For M1, = 5; M2, = 12; M3, = 9; M4, = 9; and M5, = 4. In the bottom traces, to record bipolar-driven light responses, ipRGCs were voltage clamped at the reversal potential for chloride (ECl). For M1, = 10; M2, = 10; M3, = 13; M4, = 8; and M5, = 4. The horizontal dashed lines indicate prestimulus baselines.