Antidepressant-like effect of Canavalia brasiliensis (ConBr) lectin in mice: Evidence for the involvement of the glutamatergic system

被引:25
作者
Rieger, Debora K. [1 ]
Costa, Ana Paula [1 ]
Budni, Josiane [1 ]
Moretti, Morgana [1 ]
Rocha Barbosa, Sabrina Giovana [1 ]
Nascimento, Kyria S. [2 ]
Teixeira, Edson H. [2 ]
Cavada, Benildo S. [2 ]
Rodrigues, Ana Lucia S. [1 ]
Leal, Rodrigo B. [1 ]
机构
[1] Univ Fed Santa Catarina, Ctr Ciencias Biol, Dept Bioquim, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Fed Ceara, BioMolLab, BR-60455970 Fortaleza, CE, Brazil
关键词
ConBr; Lectin; Depression; NMDA; Nitric oxide; Forced swimming test; GUANOSINE-MONOPHOSPHATE PATHWAY; OXIDE-CGMP PATHWAY; NITRIC-OXIDE; NMDA RECEPTORS; ASCORBIC-ACID; DEPRESSION; PLASMA; FLUOXETINE; CITALOPRAM; PROTECTS;
D O I
10.1016/j.pbb.2014.03.008
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Lectins recognize and reversibly bind to carbohydrates attached to proteins and lipids modulating a variety of signaling pathways. We previously showed that ConBr, a lectin from Canavalia brasiliensis seeds, produced an antidepressant-like effect in mice by modulating the monoaminergic neurotransmitter systems. Moreover, ConBr blocked hippocampal neurotoxicity induced by quinolinic acid in vivo and by glutamate in vitro, suggesting a neuroprotective activity of ConBr via glutamatergic system modulation. Therefore, the present study was undertaken to investigate the involvement of the N-methyl-D-aspartate (NMDA) receptor and the L-arginine-nitric oxide (NO) pathway in the antidepressant-like action displayed by ConBr in the forced swimming test (FST). With the aim of verifying the involvement of NMDA receptors in the antidepressant-like effect of ConBr (10 mu g/site, i.c.v.), an intra-cerebroventricular (tor.) pretreatment with either NMDA (0.1 pmol/site) or D-serine (30 mu g/site) was carried out. The results show that both treatments blocked the effect of ConBr. Furthermore, the coadministration of subeffective doses of the NMDA receptor antagonist MK-801 (0.001 mg/kg, i.p.) or ketamine (0.1 mg/kg, i.p.; NMDA receptor antagonist) and ConBr (0.1 mu g/site, i.c.v.) caused a synergistic reduction in immobility time. In order to verify the dependence of the L-arginine-NO-cGMP pathway, on the effect of ConBr in the FST, a pretreatment with the NO precursor, L-arginine (750 mg/kg, i.p.), or the PDE5 inhibitor, sildenafil (5 mg/kg, i.p.), was performed. Both drugs abolished the antidepressant-like action of ConBr. Finally, the administration of subeffective doses of the soluble guanylate cyclase inhibitor 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ; 30 pmol/site, i.c.v.) and ConBr (0.1 mu g/site, i.c.v.) produced a synergistic antidepressant-like effect in the FST. Taken together, the results suggest that the antidepressant-like effect of ConBr in the FST involves NMDA receptor inhibition and reduction in NO and cGMP synthesis. (C) 2014 Elsevier Inc All rights reserved.
引用
收藏
页码:53 / 60
页数:8
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