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. 2019 May 7;10(5):364. doi: 10.1038/s41419-019-1576-3

Fig. 5. Activating TRPV4 enhances membrane excitability of parasol ganglion cells.

Fig. 5

Na currents (INa) mediated by voltage-gated Na channels were recorded under whole-cell voltage-clamp mode from flat mount retinas. Electric pulses were used to hold the membrane potential from a baseline level of −110 mV (b and c) or −70 mV (d) to a series of Vh. The INa is activated at Vh ≈ −50 mV (c). The application of TRPV4 agonist 4αPDD 1 μM in the bath does not clearly alter the activation curve (c) or peak amplitude of INa (b), while the delay time (T) of INa is shortened for all suprathreshold stimuli (d). The relationship of T and Vh is significantly altered (p < 0.05 for both T and τ) (For definitions of τ see methods). In a, the arrow depicts the axon, and the scale bar is 20 μm. The chloride equilibrium potential is −61 mV. Vh-holding potential