Volume 17, Number 11,
Issue of June 1, 1997
pp. 4406-4414
Copyright ©1997 Society for Neuroscience
Temperature Dependency of Basal and Evoked Release of Amino Acids
and Calcitonin Gene-Related Peptide from Rat Dorsal Spinal Cord
Received Jan. 17, 1997; revised March 3, 1997; accepted March 12, 1997.
David M. Dirig1,
Xiao-Ying Hua2, and
Tony L. Yaksh1, 2
Departments of 1 Pharmacology and
2 Anesthesiology, University of California, San Diego, La
Jolla, California 92093-0818
Moderate hypothermia significantly diminishes consequences of
spinal and cerebral anoxia. One component of this neuroprotection has
been hypothesized to be suppression of excitotoxic transmitter release.
Whether this suppression is attributable to reduced hypoxic injury that
induces release or an alteration of the release process itself is
unclear. We sought to characterize the temperature sensitivity (Q10) of basal and evoked calcitonin
gene-related peptide (CGRP) and amino acid release from dorsal horn
slices of rat spinal cord over a range of temperatures from 40 to
8°C. At 40°C, potassium (60 mM) and capsaicin (10 µM) evoked a 21- and 32-fold increase in basal CGRP
concentrations, respectively. Capsaicin had no effect on glutamate
release, but potassium evoked a 2.7-fold increase. Release evoked by
either potassium or capsaicin was reduced in a biphasic fashion with
declining temperature. Over the range of 40 to 34°C, the
Q10 values for evoked release for CGRP were 11.3 (potassium) and 39.7 (capsaicin) and for glutamate, 5.5 (potassium). Over the range of 34 to 8°C,
Q10 values were near unity for all evoked
release (0.8 and 1.3 for CGRP and 1.2 for glutamate). Although serine,
glycine, glutamine, taurine, and citrulline showed no evoked release,
basal levels were reduced at temperatures below 34°C. The pronounced
temperature dependency of evoked transmitter release between 40 and
34°C is consistent with the profound cerebral protection observed
with mild hypothermia in which metabolic activity is only slightly
depressed.
Key words:
hypothermia;
hyperthermia;
glutamate;
CGRP;
spinal cord
superfusion;
evoked transmitter release;
dorsal horn;
capsaicin