The effect of µ-opioid receptor activation on GABAergic neurons in the spinal dorsal horn.
10.4196/kjpp.2018.22.4.419
- Author:
Yoo Rim KIM
1
;
Hyun Geun SHIM
;
Chang Eop KIM
;
Sang Jeong KIM
Author Information
1. Department of Physiology, Seoul National University College of Medicine, Seoul 03080, Korea. sangjkim@snu.ac.kr
- Publication Type:Original Article
- Keywords:
DAMGO;
GABAergic interneurons;
Opioid;
Pain;
Substantia gelatinosa
- MeSH:
Analgesics, Opioid;
Animals;
Enkephalin, Ala(2)-MePhe(4)-Gly(5)-;
Excitatory Postsynaptic Potentials;
GABAergic Neurons*;
Interneurons;
Mice;
Mice, Transgenic;
Nerve Fibers, Unmyelinated;
Neurons;
Spinal Cord;
Spinal Cord Dorsal Horn*;
Substantia Gelatinosa;
Synaptic Transmission
- From:The Korean Journal of Physiology and Pharmacology
2018;22(4):419-425
- CountryRepublic of Korea
- Language:English
-
Abstract:
The superficial dorsal horn of the spinal cord plays an important role in pain transmission and opioid activity. Several studies have demonstrated that opioids modulate pain transmission, and the activation of µ-opioid receptors (MORs) by opioids contributes to analgesic effects in the spinal cord. However, the effect of the activation of MORs on GABAergic interneurons and the contribution to the analgesic effect are much less clear. In this study, using transgenic mice, which allow the identification of GABAergic interneurons, we investigated how the activation of MORs affects the excitability of GABAergic interneurons and synaptic transmission between primary nociceptive afferent and GABAergic interneurons. We found that a selective µ-opioid agonist, [D-Ala², NMe-Phe⁴, Gly-ol]-enkephanlin (DAMGO), induced an outward current mediated by K⁺ channels in GABAergic interneurons. In addition, DAMGO reduced the amplitude of evoked excitatory postsynaptic currents (EPSCs) of GABAergic interneurons which receive monosynaptic inputs from primary nociceptive C fibers. Taken together, we found that DAMGO reduced the excitability of GABAergic interneurons and synaptic transmission between primary nociceptive C fibers and GABAergic interneurons. These results suggest one possibility that suppression of GABAergic interneurons by DMAGO may reduce the inhibition on secondary GABAergic interneurons, which increase the inhibition of the secondary GABAergic interneurons to excitatory neurons in the spinal dorsal horn. In this circumstance, the sum of excitation of the entire spinal network will control the pain transmission.
