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Antidepressant-like effect of the extract of Rosmarinus officinalis in mice: Involvement of the monoaminergic system
Authors:Daniele G Machado  Luis EB Bettio  Mauricio P Cunha  Juliano C Capra  Juliana B Dalmarco  Moacir G Pizzolatti  Ana Lúcia S Rodrigues
Institution:1. Departamento de Bioquímica, Centro de Ciências Biológicas, Universidade Federal de Santa Catarina, Brazil;2. Departamento de Química, Centro de Ciências Físicas e Matemáticas, Universidade Federal de Santa Catarina, Campus Universitário, Trindade, 88040-900, Florianópolis-SC, Brazil
Abstract:Rosemary, Rosmarinus officinalis L. (Labiatae) has several therapeutic applications in folk medicine in curing or managing a wide range of diseases, including depression. In this study, the effect of the hydroalcoholic extract of the stems and leaves of this plant was investigated in two behavioral models, the forced swimming test (FST) and tail suspension test (TST) in mice. The extract of R. officinalis produced an antidepressant-like effect, since the acute treatment of mice with the extract by p.o. route significantly reduced the immobility time in the FST (100 mg/kg) and TST (10–100 mg/kg), as compared to a control group, without accompanying changes in ambulation in the open-field test. Moreover, the repeated administration (14 days) of the hydroalcoholic extract of R. officinalis by p.o. route also produced an antidepressant-like effect in the TST (100–300 mg/kg). The pretreatment of mice with p-chlorophenylalanine (PCPA, 100 mg/kg, i.p., an inhibitor of serotonin synthesis, for 4 consecutive days), NAN-190 (0.5 mg/kg, i.p., a 5-HT1A receptor antagonist), ketanserin (5 mg/kg, i.p., a 5-HT2A receptor antagonist), 1-(m-chlorophenyl) biguanide (mCPBG, 10 mg/kg, i.p., a 5-HT3 receptor agonist), prazosin (1 mg/kg, i.p., an α1-adrenoceptor antagonist), SCH23390 (0.05 mg/kg, s.c., a dopamine D1 receptor antagonist) or sulpiride (50 mg/kg, i.p., a dopamine D2 receptor antagonist), but not yohimbine (1 mg/kg, i.p., an α2-adrenoceptor antagonist) was able to reverse the anti-immobility effect of the extract (10 mg/kg, p.o.) in the TST. The combination of MDL72222, (0.1 mg/kg, i.p., a 5-HT3 receptor antagonist) with a sub-effective dose of the extract of R. officinalis (1 mg/kg, p.o.) produced an anti-immobility effect in the TST. The results suggest that the antidepressant action of the extract of R. officinalis is mediated by an interaction with the monoaminergic system and that this plant should be further investigated as an alternative therapeutic approach for the treatment of depression.
Keywords:ANOVA  analysis of variance  mCPBG  1-(m-chlorophenyl) biguanide  DMSO  dimethylsulfoxide  FST  forced swimming test  MAOi  monoamine oxidase inhibitor  MDL72222  tropanyl 3  5-dichlorobenzoate  NAN-190  1-(2-methoxyphenyl)-4[-(2-phthalimido)butyl]piperazine)  NA  noradrenaline  PCPA  p-chlorophenylalanine methyl ester  SCH23390  (R)-(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2  3  4  5-tetrahydro-1H-3-benzazepine hydrochloride  5-HT  serotonin  SSRI  selective serotonin reuptake inhibitor  TST  tail suspension test
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