Antidepressant-like effect of lectin from Canavalia brasiliensis (ConBr) administered centrally in mice

被引:52
作者
Barauna, Sara C.
Kaster, Manuella P.
Heckert, Bettina T.
do Nascimento, Kyria S.
Rossi, Francesco M.
Teixeira, Edson H.
Cavada, Benildo S.
S Rodrigues, Ana Lucia
Leal, Rodrigo B. [1 ]
机构
[1] Univ Fed Santa Catarina, Dept Biol, Ctr Ciencias Biol, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Federal Ceara, BioMol Lab, BR-60455970 Fortaleza, Ceara, Brazil
[3] Univ Fed Ceara, Fac Med Sobral, BR-62041180 Sobrai, Ce, Brazil
关键词
lectin; ConBr; ConA; forced swimming test; antidepressant; monoaminergic system; 5-HT; dopamine; noradrenaline;
D O I
10.1016/j.pbb.2006.07.030
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 [法学]; 0303 [社会学]; 030303 [人类学]; 04 [教育学]; 0402 [心理学];
摘要
This study investigates the action of the central administration of the lectins isolated from Canavalia brasiliensis seeds (ConBr) and from Canavalia ensiformes seeds, (Concanavalin A, ConA) in the forced swimming test (FST) in mice. ConBr (1-10 mu g/site, i.c.v.), but not ConA, produced a decrease in the immobility time in the FST (observed at the time points 15, 30, 60 and 120 min after the injection), without changing the locomotor activity in the open-field test. The effect of ConBr in the FST was dependent on its protein structure integrity. ConBr (0.1 mu g/site, i.c.v.) caused a potentiation of the action of fluoxetine, a selective 5-HT reuptake inhibitor. The anti-immobility effect elicited by ConBr(0.1 mu g/site, i.c.v.) in the FST was prevented by the pretreatment of mice with pindolol (32 mg/kg, a 5-HT1A/1B receptor/beta-adrenoceptor antagonist), NAN-190 (0.5 mg/kg, a 5-HT1A receptor antagonist), ketanserin (5 mg/kg, a 5-HT2A/2C receptor antagonist), sulpiride (50 mg/kg, a D-2 receptor antagonist) or yohimbine (1 mg/kg, an alpha(2)-adrenoceptor antagonist), but not with SCH 23390 (0.05 mg/kg, a D-1 receptor antagonist) or prazosin (1 mg/kg, an alpha(1)-adrenoceptor antagonist). These results indicate that the antidepressant-like effect of ConBr in the FST is dependent on its interaction with the serotoninergic (via 5-HT1A and 5-HT2), noradrenergic (via alpha(2)-adrenoceptors) and dopaminergic (via D-2 receptors) systems. Considering the presence of lectins in the brain and based on the results, it will be important to determine a possible role of endogenous lectins in the modulation of the central nervous system function. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:160 / 169
页数:10
相关论文
共 62 条
[1]
Lectin-induced nitric oxide production [J].
Andrade, JL ;
Arruda, S ;
Barbosa, T ;
Paim, L ;
Ramos, MV ;
Cavada, BS ;
Barral-Netto, M .
CELLULAR IMMUNOLOGY, 1999, 194 (01) :98-102
[2]
In vivo lymphocyte activation and apoptosis by lectins of the Diocleinae subtribe [J].
Barbosa, T ;
Arruda, S ;
Cavada, B ;
Grangeiro, TB ;
de Freitas, LAR ;
Barral-Netto, M .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2001, 96 (05) :673-678
[3]
BECKER JW, 1975, J BIOL CHEM, V250, P1513
[4]
RAT PAW EDEMA AND LEUKOCYTE IMMIGRATION INDUCED BY PLANT-LECTINS [J].
BENTO, CAM ;
CAVADA, BS ;
OLIVEIRA, JTA ;
MOREIRA, RA ;
BARJAFIDALGO, C .
AGENTS AND ACTIONS, 1993, 38 (1-2) :48-54
[5]
New approaches to antidepressant drug discovery: beyond monoamines [J].
Berton, O ;
Nestler, EJ .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (02) :137-151
[6]
CURRENT ADVANCES AND TRENDS IN THE TREATMENT OF DEPRESSION [J].
BLIER, P ;
DEMONTIGNY, C .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1994, 15 (07) :220-226
[7]
Boehm S, 1998, J NEUROCHEM, V71, P2421
[8]
Revisiting proteus:: Do minor changes in lectin structure matter in biological activity?: Lessons from and potential biotechnological uses of the diocleinae subtribe lectins [J].
Cavada, BS ;
Barbosa, T ;
Arruda, S ;
Grangeiro, TB ;
Barral-Netto, M .
CURRENT PROTEIN & PEPTIDE SCIENCE, 2001, 2 (02) :123-135
[9]
CEBO C, 2002, BIOCHIM BIOPHYS ACTA, V19, P422
[10]
Characterization of serotonin transporter in blood lymphocytes of rats.: Modulation by in vivo administration of mitogens [J].
Cedeño, N ;
Urbina, M ;
Obregón, F ;
Lima, L .
JOURNAL OF NEUROIMMUNOLOGY, 2005, 159 (1-2) :31-40