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Inhibition of N-methyl-D-aspartate receptor function appears to be one of the common actions for antidepressants

You-Zhi Zhang

Yan-Qin Liu

Division of Psychopharmacology, Beijing Institute of Pharmacology and Toxicology, Beijing, China

Heng-Lin Wang

Department of Anesthesiology, 309 Hospital of Beijing, China

Jiang-Bei Cao

Ting-Ting Guan

Zhi-Pu Luo

Division of Psychopharmacology, Beijing Institute of Pharmacology and Toxicology, Beijing, China

In order to explore the possible common action mechanisms of three kinds of classical antidepressants, inhibition of drugs on the N-methyl-D-aspartate (NMDA)–Ca²–nitric oxide synthase (NOS) signal pathway was observed. With 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay and lactic dehydrogenase (LDH) assay, classical antidepressants, desipramine (1, 10 M), fluoxetine (0.625–10 M) or moclobemide (2.5, 10 M) antagonized NMDA 300 M induced-lesion in PC12 cells. Using fura-2/AM (acetoxymethyl ester) labelling assay, desipramine or fluoxetine at doses 1, 5 M attenuated the intracellular Ca² overload induced by NMDA 200 M for 24h in PC12 cells. Meanwhile, using confocal microscope, it was also found that desipramine 5 M, fluoxetine 2.5 M or moclobemide 10 M decreased the NMDA 20 M induced intracellular Ca² overload in primarily cultured rat hippocampal neurons. Furthermore, desipramine (1, 5 M), fluoxetine (1, 5 M) or moclobemide (2.5, 10 M) significantly inhibited NOS activity in NMDA (300 M) treated PC12 cells for 4h. In summary, we suggest that inhibition on the function of NMDA–Ca² –NOS signal pathway appears to be one of the common actions for antidepressants despite their remarkably different structures, which is expected to have great implication for the evaluation and screening in vitro of new antidepressants.

Key Words: antidepressants • PC12 cells • N-methyl-D-aspartate • Ca2 • nitric oxide synthase • hippocampal neurons

This version was published on September 1, 2006

Journal of Psychopharmacology, Vol. 20, No. 5, 629-635 (2006)
DOI: 10.1177/0269881106059692


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