TY - JOUR
T1 - Neuropharmacological effects of sigma receptor ligands
T2 - Anxiolytic, anti-amnesic and neuroprotective effects
AU - Amano, M.
AU - Yamada, K.
AU - Matsuno, K.
AU - Nabeshima, Toshitaka
PY - 1996
Y1 - 1996
N2 - There is evidence for the existence of two classes of sigma binding sites, termed 'site 1' and 'site 2', that are distinct from opioid and PCP receptors. Sigma receptor ligands may be useful in the treatment of schizophrenia, since they improve not only positive but also negative symptoms with little extrapyramidal side effects in animal models. In addition, recent experiments have demonstrated that sigma receptor ligands attenuate the motor suppression and colonic motor disturbances seen under menially stressful situations, stimulate the central cholinergic function thereby ameliorating impairment of learning and memory, and protect cerebral neurons against cerebral ischemic insult. The present review describes the neuropharmacological effects of sigma receptor ligands, especially anxiolytic (anti-stress) effects, ameliorating effects on impairment of learning and memory, and neuroprotective effects.
AB - There is evidence for the existence of two classes of sigma binding sites, termed 'site 1' and 'site 2', that are distinct from opioid and PCP receptors. Sigma receptor ligands may be useful in the treatment of schizophrenia, since they improve not only positive but also negative symptoms with little extrapyramidal side effects in animal models. In addition, recent experiments have demonstrated that sigma receptor ligands attenuate the motor suppression and colonic motor disturbances seen under menially stressful situations, stimulate the central cholinergic function thereby ameliorating impairment of learning and memory, and protect cerebral neurons against cerebral ischemic insult. The present review describes the neuropharmacological effects of sigma receptor ligands, especially anxiolytic (anti-stress) effects, ameliorating effects on impairment of learning and memory, and neuroprotective effects.
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M3 - Review article
C2 - 8905794
AN - SCOPUS:0029848493
SN - 1340-2544
VL - 16
SP - 73
EP - 84
JO - Japanese Journal of Psychopharmacology
JF - Japanese Journal of Psychopharmacology
IS - 3
ER -