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Vol. 294, Issue 2, 500-509, August 2000
Departments of Neurology and Pharmacology & Physiology, University
of Rochester School of Medicine & Dentistry, Rochester, New York
The cellular correlates of desensitization or tolerance are poorly
understood. To address this, we studied acute and long-term µ-opioid
desensitization, with respect to Ca2+ currents, in cultured
rat dorsal root ganglion (DRG) neurons. Exposure of DRG neurons to the
µ-agonist
[D-Ala2,N-MePhe4,Gly-ol5]-enkephalin
(DAMGO; 3 µM) reduced whole-cell currents ~35%, but with continued
agonist application, 52% of the response was lost over 10 to 12 min.
In contrast, exposure of DRG neurons to DAMGO for 24 h resulted in
a nearly complete loss of Ca2+ channel regulation after
washing and re-exposure to DAMGO. Responses to the
-aminobutyric
acidB agonist baclofen were not affected in these
neurons. Acute desensitization preferentially affected the
voltage-sensitive component of µ-opioid and
-aminobutyric acidB responses. Facilitation of both the DAMGO- and
baclofen-inhibited current by a strong depolarizing prepulse was
significantly attenuated in acutely desensitized neurons. Because
G
-subunits mediate
neurotransmitter-induced changes in channel voltage-dependent properties, these data suggest an altered interaction of the
G
-subunit with the Ca2+
channel. Block of N-type Ca2+ channels with
-conotoxin
GVIA revealed a component of the opioid response that did not
desensitize over 10 min. We conclude that acute and long-term
µ-opioid desensitization in DRG neurons occurs by different
mechanisms. Acute desensitization is heterologous and functionally
compartmentalized: the pathway targeting non-N-type channels is
relatively resistant to the early effects of continuous agonist
exposure; the pathway targeting N-type channels in a largely voltage-insensitive manner is partially desensitized; and the pathway
targeting N-type channels in a largely voltage-sensitive manner is
completely desensitized.
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