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The Journal of Neurophysiology Vol. 81 No. 5 May 1999, pp. 2493-2500
Copyright ©1999 by the American Physiological Society
Biology Department, University of Victoria, Victoria, British Columbia V8W 3N5, Canada
Paul, Dorothy H. and
Jan Bruner.
Receptor Potentials and Electrical Properties of Nonspiking
Stretch-Receptive Neurons in the Sand Crab Emerita
analoga (Anomura, Hippidae). J. Neurophysiol. 81: 2493-2500, 1999.
Receptor potentials and electrical properties of
nonspiking stretch-receptive neurons in the sand crab Emerita
analoga (Anomura, Hippidae). Four nonspiking, monopolar
neurons with central somata and large peripheral dendrites constitute
the sole innervation of the telson-uropod elastic strand stretch
receptor in Emerita analoga. We characterized their
responses to stretch and current injection, using two-electrode current
clamp, in intact cells and in two types of isolated peripheral
dendritic segments, one that included and one that excluded the
dendritic termini (mechanosensory membrane). The membrane potentials of
intact cells at rest (mean ± SD:
57 ± 4.4 mV,
n = 30), recorded in peripheral or neuropil processes,
are similar to the membrane potentials of isolated dendritic segments
and always less negative than membrane potentials of motoneurons and
interneurons recorded in the same preparations. Ion substitution
experiments indicate that the membrane potential is influenced strongly
by Na+ conductance, probably localized in the
mechanotransducing terminals within the elastic strand. The form of the
receptor potential in response to ramp-hold-release stretch remains the
same as stretch amplitude is varied and is not dependent on initial
membrane potential (
70 to
30 mV) or recording site: initial
depolarization (slope follows ramp of applied stretch), terminated by
rapid, partial repolarization to a plateau (delayed depolarization)
that is intermediate between the peak depolarization and the initial
potential and sustained for the duration of the stretch. Responses to
depolarizing current pulses are similar to stretch-evoked receptor
potentials, except for small amplitude stimuli: an initial peak occurs
only in response to stretch and probably reflects elastic recoil of the
extracellular matrix surrounding the dendritic terminals. The rapid,
partial repolarization depends on holding potential and is abolished by
4-aminopyridine (4-AP; 10 mM), implicating a fast-activating,
fast-inactivating K+ conductance; TEA (60 mM) abolishes the
remaining slow repolarization to the plateau. In intact cells, but not
dendritic segments, regenerative depolarizations can arise in response
to stretch or depolarizing current pulses; they are reduced by
CdCl2 (10 µM) in the saline containing TEA and 4-AP and
probably reflect current spread from Ca2+ influx at
presynaptic terminals in the ganglion. We found no evidence for other
voltage-activated conductances. Unlike morphologically similar
"nonspiking" thoracic receptors of other species, E. analoga's nonspiking neurons are electrically compact and do not
boost the analogue afferent signal by voltage-activated inward
currents. The most prominent (only?) voltage-activated extra-ganglionic conductances are for potassium; by reducing the slope of the
stretch-plateau depolarization curve, they extend each neuron's
functional range to the full range of sensitivity of the receptor.
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