Transduction and adaptation in spider slit sense organ mechanoreceptors

1. Mechanoreceptor neurons in spider (Cupiennius salei) slit sense organ were examined by intracellular current- and voltage clamp recordings. Steps and pseudorandomly modulated displacement stimuli were delivered to the mechanosensitive cuticular slits. The resulting responses were used to determine the response dynamics and signal-to-noise ratio (SNR) of mechanoelectrical transduction. 2. Neurons were separated into two groups that, in terms of their afferent discharges, displayed different adaptations to displacement stimuli. Both responded at the onset of the step but then adapted fully, either immediately or within 10-200 ms. Voltage-clamp recordings showed only small differences in the receptor currents of the two groups. 3. Displacement of the slit caused a large inward current that decayed in seconds to a steady level of ~10-25% of the initial transient. When adapted to a steady displacement, the neurons responded to superimposed displacements in the same direction with additional transient currents, whose decay could be fitted by two exponentials with time constants of ~10 and 100 ms. In contrast, displacement in the opposite direction caused small 'outward' currents without obvious adaptation. This behavior persisted with increasing background displacements, suggesting a shift in the displacement- response curve along the displacement axis. 4. White noise stimulation supported the step data and confirmed that the receptor's sensitivity was independent of mean slit membrane displacement. When the relative displacement of the stimulus (i.e., strain) was held constant at different maintained backgrounds, the SNR of the neurons remained fairly constant at ~2-10 over the frequency range from 4 to 450 Hz. The receptor current frequency responses showed high-pass characteristics, with a two- to sevenfold enhancement of the response amplitude and a phase lag relative to the stimulus of 90° at 300 Hz. Low coherence values in the frequency range of 0.5-125 Hz were explained by nonlinear adaptation. 5. We conclude that, by rapidly adapting to the mean displacement of the slit membrane, slit organ mechanoreceptor neurons maintain a high sensitivity and SNR that allow the detection of small and rapid changes in cuticular strain.