Operant self-administration of a sigma ligand improves nociceptive and emotional manifestations of neuropathic pain

• Published in: European journal of pain 2013-07, Vol.17 (6), p.832-843
• Main Authors: Bura, A.S., Guegan, T., Zamanillo, D., Vela, J.M., Maldonado, R.
• Format: Article
• Language: English
• Subjects: Analgesics - therapeutic use; Analgèsics; Animals; Disease Models, Animal; Emotions; Hyperalgesia - complications; Hyperalgesia - drug therapy; Ligands; Male; Mice; Mice, Inbred C57BL; Neuralgia - chemically induced; Neuralgia - complications; Neuralgia - drug therapy; Neuràlgia; Pain Measurement - methods; Pain Threshold - drug effects; Receptors, sigma - antagonists & inhibitors; Self Administration; Sigma-1 Receptor; Ús terapèutic
• ISSN: 1090-3801; 1532-2149
• DOI: 10.1002/j.1532-2149.2012.00251.x

Background The treatment of neuropathic pain is unsatisfactory at the present moment and the sigma 1 receptor has been identified as a new potential target for neuropathic pain. The aim of this study was to use an operant self‐administration model to reveal the potential interest of a new sigma 1 receptor antagonist, S1RA, in chronic pain that was developed in mice by a partial ligation of the sciatic nerve. Methods Once that chronic pain had reached a steady state, mice were trained to maintain an operant behaviour to self‐administer S1RA. The possible abuse liability of the analgesic compound was determined by evaluating operant self‐administration in sham‐operated mice. The influence of S1RA on the anhedonic state related to chronic pain was also evaluated by measuring the preference for palatable drink (2% sucrose solution) using a recently validated and highly sensitive behavioural device. Results Nerve‐injured mice, but not sham‐operated animals, acquired the operant responding to obtain S1RA (6 mg/kg/infusion). After 10 days of S1RA self‐administration, neuropathic pain was significantly reduced in nerve‐injured mice. In addition, an anhedonic state was revealed in nerve‐injured mice by a decreased consumption of palatable drink, which was significantly attenuated by S1RA (25 mg/kg). Conclusions These results reveal the analgesic efficacy of the sigma antagonist, S1RA, in neuropathic pain associated with an improvement of the emotional negative state and that was devoided of reinforcing effects. The operant responses evaluated in this new mouse model can have a high predictive value to estimate the clinical benefit/risk ratio of new analgesic compounds to treat chronic pain, such as S1RA.