Martin-Fardon Rémi, Maurice Tangui, Aujla Harinder, Bowen Wayne D, Weiss Friedbert
Molecular and Integrative Neurosciences Department, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Neuropsychopharmacology. 2007 Sep;32(9):1967-73. doi: 10.1038/sj.npp.1301323. Epub 2007 Jan 31.
Growing evidence suggests a role for sigma(1) (sigma(1)) receptors in cognitive function, anxiety, depression, regulation of stress responses, and, recently, the appetitive effects of cocaine as measured by conditioned place preference. This study was designed to extend understanding of the role of sigma(1) receptors in addiction-relevant conditioned effects of cocaine by testing the effects of a potent and selective sigma(1) receptor antagonist, BD1047, on conditioned reinstatement of cocaine-seeking. To determine whether modification of conditioned reinstatement by BD1047 is selective for drug-directed behavior or reflects general suppressant effects on motivated behavior, BD1047 was tested also on reinstatement induced by stimuli conditioned to a natural reward, sweetened condensed milk (SCM). Additionally, because sigma(1) receptors have been implicated also in processes linked to the acute reinforcing actions of cocaine, tests of the effects of BD1047 on cocaine self-administration-including a comparison with the sigma(1) antagonist effects on SCM self-administration-were conducted as well. Cocaine self-administering male Wistar rats were trained to associate a discriminative stimulus (S(D)) with the availability of cocaine or SCM, and then subjected to reinstatement tests following extinction of cocaine or SCM-reinforced behavior. BD1047 (1-30 mg/kg) reversed response reinstatement induced by the cocaine S(D) at 20 and 30 mg/kg but did not modify SCM S(D)-induced responding at all but the highest 30 mg dose, at which responding was reversed to extinction levels. BD1047 did not modify responding reinforced directly by SCM or cocaine. The findings support a role for sigma(1) receptors in regulating conditioned responses to cocaine-related contextual stimuli and identify this receptor as a potential treatment target for the prevention of craving and relapse.
越来越多的证据表明,σ1受体在认知功能、焦虑、抑郁、应激反应调节以及最近通过条件性位置偏好测量的可卡因的奖赏效应中发挥作用。本研究旨在通过测试一种强效且选择性的σ1受体拮抗剂BD1047对可卡因觅求条件性恢复的影响,来扩展对σ1受体在可卡因成瘾相关条件性效应中作用的理解。为了确定BD1047对条件性恢复的改变是对药物导向行为具有选择性,还是反映了对动机行为的一般抑制作用,还对BD1047在由与天然奖赏——甜炼乳(SCM)相关的条件刺激诱导的恢复方面进行了测试。此外,由于σ1受体也与可卡因的急性强化作用相关的过程有关,因此还进行了BD1047对可卡因自身给药影响的测试——包括与σ1拮抗剂对SCM自身给药影响的比较。对可卡因自身给药的雄性Wistar大鼠进行训练,使其将辨别性刺激(S(D))与可卡因或SCM的可得性联系起来,然后在可卡因或SCM强化行为消退后进行恢复测试。BD1047(1 - 30mg/kg)在20和30mg/kg时可逆转由可卡因S(D)诱导的反应恢复,但除了最高的30mg剂量外,对SCM S(D)诱导的反应没有影响,在该剂量下反应逆转至消退水平。BD1047对由SCM或可卡因直接强化的反应没有影响。这些发现支持了σ1受体在调节对可卡因相关情境刺激的条件反应中的作用,并确定该受体是预防渴望和复发的潜在治疗靶点。