| Interaction of apical and basal membrane ion channels underlies electroreception in ampullary epithelia of skates Biophysical Journal, Volume 67, Issue 4, 1 October 1994, Pages 1525-1533 J. Lu and H.M. Fishman Abstract The exquisite sensitivity of elasmobranch fishes to electric fields is thought to reside in electroreceptive organs called ampullae of Lorenzini. We measured the stimulus-response behavior of ampullary organs excised from skates. Under open-circuit conditions, the ampullary organ showed three distinct response states: spontaneous repetitive spikes, evoked spikes, and small, damped oscillatory responses. Under short-circuit conditions, the amplitude range for a linear current response to a sinusoidal (0.5 Hz) voltage clamp of an organ (assessed by spectral analysis of the harmonics generated) was 7–200 microV rms. Changes in the spike firing rate of the afferent nerve innervating the organ were evident for voltage clamps of the ampullary epithelium of 3 microV and the spike rate saturated for clamp steps exceeding 100 microV. Thus, the linear response range of the ampullary epithelium exceeded the range in spike firing rate of the afferent nerve. The steady-state transorgan electrical properties under voltage clamp conditions were obtained by analysis of complex admittance determinations in the frequency range 0.05–20 Hz for perturbations (< 100 microV rms) in the linear range. Admittance functions were distinctly related to the preparation states observed under open-circuit conditions. A negative real part in the organ admittance (i.e., a steady-state negative conductance generated by the preparation) was a common characteristic of the two (open-circuit) excitable states. The negative conductance was also confirmed by the direction of current flow through the ampullary epithelium in response to step voltage clamps.(ABSTRACT TRUNCATED AT 250 WORDS) Abstract | PDF (870 kb) |
| Localization and function of the electrical oscillation in electroreceptive ampullary epithelium from skates Biophysical Journal, Volume 69, Issue 6, 1 December 1995, Pages 2458-2466 J. Lu and H.M. Fishman Abstract A steady, spontaneous current oscillation (1 nA p-p) occurs in voltage-clamped, isolated ampullary organs (canal, ampulla, and nerve) from skates (Raja). Spectral analysis showed that energy in the oscillation was confined to a narrow band of frequencies (3 Hz) about a fundamental frequency (32 Hz at 20 degrees C) and in harmonics. The frequency of the oscillation was temperature dependent (increasing from 21 to 33 Hz for increases in temperature from 13 degrees C to 21 degrees C). The addition of 0.5 microM tetrodotoxin to the basal side of the ampullary epithelium eliminated afferent nerve activity but had no effect on the epithelial oscillation, indicating that the oscillation is not generated or induced by afferent nerve activity. Nitrendipine (2 microM) added to the solution bathing the basal side of the ampullary epithelium abolished the oscillation rapidly (within minutes), but a steady-state negative conductance (i.e., real part of the complex admittance < 0) generated by the preparation remained for 36min. Conversely, nitrendipine (50 microM) added to the perfusate (artificial sea water) of the apical side eliminated the negative conductance rapidly (18.5 min) but had no effect on the spontaneous oscillation for more than 1 h. The effect and the elapsed time for an effect of nitrendipine after separate applications to the basal and apical membrane surfaces of ampullary epithelium suggest that 1) the negative conductance and the oscillation are generated independently in apical and basal membranes, respectively, and 2) both processes involve L-type Ca channels. Furthermore, the addition of tetraethylammonium (2 mM) to the basal side eliminated both the oscillation and the postsynaptic response to voltage clamps (< or = 100 microV) of the ampullary epithelium in the operational voltage range of the afferent nerve. This result suggests that the basal membrane oscillation functions in neurotransmitter release from presynaptic (basal) membranes. Abstract | PDF (1007 kb) |
| A Comment on the Sensitivity of Fish to Low Electric Fields Biophysical Journal, Volume 75, Issue 4, 1 October 1998, Pages 2117-2118 Donatella Petracchi and Giovanni Cercignani Full Text | PDF (74 kb) |
Copyright © 1995 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 69, Issue 6, 2467-2475, 1 December 1995
doi:10.1016/S0006-3495(95)80117-7
Research Article
J. Lu and H.M. Fishman
Two ampullary epithelial properties necessary for electroreception were used to identify the types of ion channels and transporters found in apical and basal membranes of ampullary receptor cells of skates and to assess their individual role under voltage-clamp conditions. The two essential properties are (1) a steady-state negative conductance generated in apical membranes and (2) a small, spontaneous current oscillation originating in basal membranes (Lu and Fishman, 1995). The effects of pharmacological agents and ion substitutions on these properties were evaluated from transorgan or transepithelial complex admittance determinations in the frequency range 0.125 to 50 Hz measured in individual, isolated ampullary organs. In apical membranes, L-type Ca channels were found to be responsible for generation of the steady-state negative conductance. In basal membranes, K and Ca-dependent Cl (Cl(Ca)) channels were demonstrated to contribute to a net positive membrane conductance. L-type Ca channels were also evident in basal membranes and are thought to function in synaptic transmission from the electroreceptive epithelium to the primary afferent nerve. In addition to ion channels in basal membranes, two transporters (Na+/K+ pump and Na(+)-Ca+ exchanger) were apparent. Rapid (minutes) cessation of the current oscillation after blockage of any of the basal ion channels (Ca, Cl(Ca), K) suggests critical involvement of each of these channel types in the generation of the oscillation. Suppression of either Na+/K+ transport or Na(+)-Ca2+ exchange also eliminated the oscillation but at a slower rate, indicating an indirect effect.