Sigma 2 Receptor/Tmem97 Agonists Produce Long Lasting Antineuropathic Pain Effects in Mice.

ABSTRACT: Neuropathic pain is an important medical problem with few effective treatments. The sigma 1 receptor (?1R) is known to be a potential target for neuropathic pain therapeutics, and antagonists for this receptor are effective in preclinical models and are currently in phase II clinical trials. Conversely, relatively little is known about ?2R, which has recently been identified as transmembrane protein 97 (Tmem97). We generated a series of ?1R and ?2R/Tmem97 agonists and antagonists and tested them for efficacy in the mouse spared nerve injury (SNI) model. In agreement with previous reports, we find that ?1R ligands given intrathecally (IT) produce relief of SNI-induced mechanical hypersensitivity. We also find that the putative ?2R/Tmem97 agonists DKR-1005, DKR-1051, and UKH-1114 (Ki ? 46 nM) lead to relief of SNI-induced mechanical hypersensitivity, peaking at 48 h after dosing when given IT. This effect is blocked by the putative ?2R/Tmem97 antagonist SAS-0132. Systemic administration of UKH-1114 (10 mg/kg) relieves SNI-induced mechanical hypersensitivity for 48 h with a peak magnitude of effect equivalent to 100 mg/kg gabapentin and without producing any motor impairment. Finally, we find that the TMEM97 gene is expressed in mouse and human dorsal root ganglion (DRG) including populations of neurons that are involved in pain; however, the gene is also likely expressed in non-neuronal cells that may contribute to the observed behavioral effects. Our results show robust antineuropathic pain effects of ?1R and ?2R/Tmem97 ligands, demonstrate that ?2R/Tmem97 is a novel neuropathic pain target, and identify UKH-1114 as a lead molecule for further development.

SUBMITTER: Sahn JJ 

PROVIDER: S-EPMC5715471 | biostudies-other | 2017 Aug

REPOSITORIES: biostudies-other