Pałucha Agnieszka, Pilc Andrzej
Department of Neurobiology, Institute of Pharmacology, Polish Academy of Sciences, Smetna 12, PL 31-343 Kraków, Poland.
Pol J Pharmacol. 2002 Nov-Dec;54(6):581-6.
Most conventional antidepressant drugs influence serotoninergic, adrenergic, and/or dopaminergic systems, increasing serotonin, norepinephrine and dopamine synaptic availability. More recently attention has focused on glutamatergic system. Both preclinical and clinical studies, showing antidepressant-like actions of compounds which reduce transmission at N-methyl-D-aspartate (NMDA) receptors, indicate possible involvement of glutamatergic system in the etiology of depression. Since glutamatergic transmission is controlled not only by ionotropic but also by metabotropic glutamate receptors (mGluR), their involvement in the etiology and the therapy of depression was also postulated. Recent studies, showing that antidepressant treatment may influence mGlu receptors, together with the findings that group I mGluR antagonists, may possess antidepressant-like action, support this hypothesis.
大多数传统抗抑郁药物会影响血清素能、肾上腺素能和/或多巴胺能系统,增加血清素、去甲肾上腺素和多巴胺的突触可用性。最近,注意力集中在了谷氨酸能系统上。临床前和临床研究均表明,能减少N-甲基-D-天冬氨酸(NMDA)受体传递的化合物具有类抗抑郁作用,这表明谷氨酸能系统可能参与了抑郁症的病因。由于谷氨酸能传递不仅受离子型谷氨酸受体控制,还受代谢型谷氨酸受体(mGluR)控制,因此也有人推测它们参与了抑郁症的病因和治疗。最近的研究表明,抗抑郁治疗可能会影响mGlu受体,同时发现I组mGluR拮抗剂可能具有类抗抑郁作用,这支持了这一假设。