The Effect of Intrathecal Injection of Dextromethorphan on the Experimental Neuropathic Pain Model

AuthorAchmad Fahmien
AuthorYunus Kuntawi Ajien
AuthorDirga Rachmad Apriantoen
AuthorAkbar Widoen
AuthorAsadullah Asadullahen
AuthorNurkholis Roufien
AuthorDanti Nur Indiastutien
AuthorHeri Subiantoen
AuthorAgus Turchanen
OrcidAchmad Fahmi [0000-0003-0464-5482]en
OrcidYunus Kuntawi Aji [0000-0002-1877-6312]en
OrcidDirga Rachmad Aprianto [0000-0003-2591-1938]en
OrcidAsadullah Asadullah [0000-0002-9368-4717]en
Issued Date2021-06-30en
AbstractBackground: Peripheral glucocorticoid receptors (GRs) are altered by peripheral nerve injury and may modulate the development of neuropathic pain. Two central pathogenic mechanisms underlying neuropathic pain are neuroinflammation and N-methyl-D-aspartate receptor (NMDAR)-dependent neural plasticity in the spinal cord. Objectives: This study examined the effect of the non-competitive NMDAR antagonist dextromethorphan on partial sciatic nerve ligation (PSL)-induced neuropathic pain and the spinal expression of the glucocorticoid receptor (GR). Methods: Male mice were randomly assigned into a sham group and two groups receiving PSL followed by intrathecal saline vehicle or dextromethorphan (iDMP). Vehicle or iDMP was administered 8 - 14 days after PSL. The hotplate paw-withdrawal latency was considered to measure thermal pain sensitivity. The spinal cord was then sectioned and immunostained for GR. Results: Thermal hyperalgesia developed similarly in the vehicle and iDMP groups prior to the injections (P = 0.828 and 0.643); however, it was completely mitigated during the iDMP treatment (P < 0.001). GR expression was significantly higher in the vehicle group (55.64 ± 4.50) than in the other groups (P < 0.001). The iDMP group (9.99 ± 0.66) showed significantly higher GR expression than the sham group (6.30 ± 1.96) (P = 0.043). Conclusions: The suppression of PLS-induced thermal hyperalgesia by iDMP is associated with the downregulation of GR in the spinal cord, suggesting that this analgesic effect is mediated by inhibiting GR-regulated neuroinflammation.en
DOIhttps://doi.org/10.5812/aapm.114318en
KeywordNeuropathic Painen
KeywordIntrathecalen
KeywordGlucocorticoid Receptoren
KeywordDextromethorphan Hydrobromideen
PublisherBrieflandsen
TitleThe Effect of Intrathecal Injection of Dextromethorphan on the Experimental Neuropathic Pain Modelen
TypeResearch Articleen

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