Ishihara Kumatoshi, Sasa Masashi
Department of Pharmacotherapy, Graduate School of Medical Sciences, Hiroshima University, 1-2-3, Kasumi, Minamiku, Hiroshima, 734-8551 Japan.
Nihon Shinkei Seishin Yakurigaku Zasshi. 2002 Feb;22(1):23-30.
Sigma receptors have recently been the target of drug development related to psychiatric disorders, including schizophrenia and depression, as well as cognitive enhancers. This paper focused on the sigma-receptor-mediated modulation of neuronal activity, especially the effects on aminergic neuron and hippocampal neuron activity. Dopaminergic neuron activities in the substantia nigra and ventral tegmental area (VTA) are variously modified by the systemic administration of sigma ligands. When applied with microiontophoresis, they are reported to increase dopaminergic neuron activity in the VTA. This activity may be involved in the psychotropic or antipsychotic effects of these ligands. Moreover, serotonergic neurons in the raphe nucleus and noradrenergic neurons in the locus coeruleus were activated by sigma ligands. These effects are probably related to the antidepressant activity of sigma receptor ligands. In the hippocampus, sigma ligands suppressed CA1 neuronal activity in vitro. The effects were suggested to be due to an increase in the threshold of action potential and decreased synaptic transmission efficacy. NMDA receptor function was modified in biphasic fashion related to doses of sigma ligands, that is, a lower dose facilitated the NMDA receptor functions, and a higher dose inhibited them. These effects on the hippocampal neurons may contribute to their neuroprotective and antiamnesic actions. Further studies are needed to elucidate the relation between the physiological function of sigma receptor and psychiatric diseases by the use of sigma receptor ligands and molecular techniques.
西格玛受体最近已成为与精神疾病(包括精神分裂症和抑郁症)以及认知增强剂相关的药物开发靶点。本文重点关注西格玛受体介导的神经元活动调节,特别是对胺能神经元和海马神经元活动的影响。黑质和腹侧被盖区(VTA)中的多巴胺能神经元活动会因全身性给予西格玛配体而发生不同程度的改变。据报道,当通过微量离子电泳应用时,它们会增加VTA中多巴胺能神经元的活动。这种活动可能与这些配体的精神otropic或抗精神病作用有关。此外,中缝核中的5-羟色胺能神经元和蓝斑中的去甲肾上腺素能神经元被西格玛配体激活。这些作用可能与西格玛受体配体的抗抑郁活性有关。在海马体中,西格玛配体在体外抑制CA1神经元活动。这些作用被认为是由于动作电位阈值增加和突触传递效率降低所致。NMDA受体功能与西格玛配体的剂量呈双相性改变,即较低剂量促进NMDA受体功能,而较高剂量则抑制它们。这些对海马神经元的作用可能有助于它们的神经保护和抗遗忘作用。需要进一步研究以利用西格玛受体配体和分子技术阐明西格玛受体的生理功能与精神疾病之间的关系。