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The Journal of Neurophysiology Vol. 81 No. 4 April 1999, pp. 1567-1574
Copyright ©1999 by the American Physiological Society
Channel Properties in Squid Motor
Neurons
Department of Physiology, University of Utah School of Medicine, Salt Lake City, Utah 84108
Petty, Christopher N. and
Mary T. Lucero.
Characterization of a Na+-dependent betaine transporter
with Cl
channel properties in squid motor neurons.
Most marine invertebrates, including squids, use transporters
to accumulate organic osmolytes such as betaine, to prevent water loss
when exposed to elevated salinity. Although a limited number of flux
studies have shown the Na+ dependence of betaine transport,
nothing is known about the electrogenic properties of osmolyte
transporters. We used whole cell and perforated-patch voltage-clamp
techniques to characterize the electrical properties of the betaine
transporter in giant fiber lobe motor neurons of the squid
Lolliguncula brevis. Betaine activated a large,
Cl
-selective current that was reversibly blocked by 100 µM niflumic acid (97 ± 2% block after 40 s, SD;
n = 7) and partially inhibited by 500 µM SITS (29 ± 11%; n = 5). The Cl
current was
Na+ dependent and was virtually eliminated by isotonic
replacement of Na+ with Li+, NMDG+,
or Tris+. Concentration-response data revealed an
EC50 in a physiologically relevant range for these animals
of 5.1 ± 0.9 mM (n = 11). In vertebrates, the
betaine transporter is structurally related to the GABA transporter,
and although GABA did not directly activate the betaine-induced
current, it reversibly reduced betaine responses by 34 ± 14%
(n = 8). Short-term changes in osmolality alone did not
activate the Cl
current, but when combined with betaine,
Cl
currents increased in hypertonic solutions and
decreased in hypotonic solutions. Activation of the betaine transporter
and Cl
current in hypertonic conditions may affect both
volume regulation and excitability in L. brevis motor
neurons. This study is the first report of a novel betaine transporter
in neurons that can act as a Cl
channel.
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