T. Kohno et al., Actions of opioids on excitatory and inhibitory transmission in substantiagelatinosa of adult rat spinal cord, J PHYSL LON, 518(3), 1999, pp. 803-813
1. The actions of opioid receptor agonists on synaptic transmission in subs
tantia gelatinosa (SG) neurones in adult (6- to 10-week-old) rat spinal cor
d slices were examined by use of the blind whole-cell patch-clamp technique
.
2. Both the mu-receptor agonist DAMGO (1 mu M) and the S-receptor agonist D
PDPE (1 mu M) reduced the amplitude of glutamatergic excitatory postsynapti
c currents (EPSCs) which were monosynaptically evoked by stimulating A delt
a afferent fibres. Both also decreased the frequency of miniature EPSCs wit
hout affecting their amplitude.
3. In contrast, the K-receptor agonist U-69593(1 mu M) had little effect on
the evoked and miniature EPSCs.
4. The effects of DAMGO and DPDPE were not seen in the presence of the mu-r
eceptor antagonist CTAP (1 mu M) and the delta-receptor antagonist naltrind
ole (1 mu M), respectively.
5. Neither DAMGO nor DPDPE at 1 mu M affected the responses of SG: neurones
to bath-applied AMPA (10 mu M).
6. Evoked and miniature inhibitory postsynaptic currents (IPSCs), mediated
by either the GABA(A) or the glycine receptor, were unaffected by the mu-,
delta- and kappa-receptor agonists. Similar results were also obtained in S
G neurones in young adult (3- to 4-week-old) rat spinal cord slices.
7. These results indicate that opioids suppress excitatory but not inhibito
ry synaptic transmission, possibly through the activation of mu- and delta-
but not kappa-receptors in adult rat spinal cord SG neurones; these action
s are presynaptic in origin. Such an action of opioids may be a possible me
chanism for the antinociception produced by their intrathecal administratio
n.