Objective: Ginsenosides, biologically active components of the root of Panax ginseng, have been reported to have therapeutic benefits in a number of disease states including psychiatric conditions such as major depressive disorder. Our objective was to determine if a standardised commercial ginseng extract, G115 (R), could reduce the signs of behavioural despair commonly observed in animal models of depression either alone or in combination with the selective serotonin reuptake inhibitor (SSRI) fluoxetine. Methods: Male Sprague-Dawley (SD) rats (N = 51) were divided into four groups: vehicle control, G115 (R) ginseng root extract, fluoxetine and fluoxetine plus G115 (R). Rats were trained to voluntarily consume treatments twice daily for 14 days and were then tested in an open field (OF), elevated plus maze (EPM) and forced swim test (FST). Post-mortem hippocampal and prefrontal cortex tissue was analysed for expression of brain-derived neurotrophic factor (BDNF) and tropomyosin receptor kinase B (TrkB) by western blot. Results: One-way Analysis of Variance revealed no significant group differences in the OF or plus-maze performance on any variable examined. In the FST, fluoxetine significantly reduced immobility time and increased latency to immobility. The effects of fluoxetine were further significantly potentiated by co-administration of G115 (R). Post-mortem tissue analysis revealed significant group differences in BDNF expression in the left hippocampus and left prefrontal cortex without any accompanying changes in TrkB expression. Conclusions: We conclude that oral G115 (R) significantly potentiates the antidepressant-like effect of fluoxetine in the FST in the absence of potentially confounding effects on locomotion and anxiety.
机构:
CINVESTAV, Dept Farmacobiol, Mexico City, DF, MexicoCINVESTAV, Dept Farmacobiol, Mexico City, DF, Mexico
Fernandez-Guasti, Alonso
Olivares-Nazario, Maribel
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CINVESTAV, Dept Farmacobiol, Mexico City, DF, Mexico
Inst Nacl Psiquiatria Ramon de la Fuente Muniz, Direcc Invest Neurociencias, Mexico City, DF, MexicoCINVESTAV, Dept Farmacobiol, Mexico City, DF, Mexico
Olivares-Nazario, Maribel
Reyes, Rebeca
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CINVESTAV, Dept Farmacobiol, Mexico City, DF, MexicoCINVESTAV, Dept Farmacobiol, Mexico City, DF, Mexico
Reyes, Rebeca
Martinez-Mota, Lucia
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Inst Nacl Psiquiatria Ramon de la Fuente Muniz, Direcc Invest Neurociencias, Mexico City, DF, MexicoCINVESTAV, Dept Farmacobiol, Mexico City, DF, Mexico
机构:
MTA SZTE, Neurosci Res Grp, Szeged, Hungary
Univ Szeged, Fac Med, Interdisciplinary Excellence Ctr, Albert Szent Gyorgyi Hlth Ctr,Dept Neurol, Szeged, HungaryMTA SZTE, Neurosci Res Grp, Szeged, Hungary
Tanaka, Masaru
Bohar, Zsuzsanna
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MTA SZTE, Neurosci Res Grp, Szeged, Hungary
Univ Szeged, Fac Med, Interdisciplinary Excellence Ctr, Albert Szent Gyorgyi Hlth Ctr,Dept Neurol, Szeged, HungaryMTA SZTE, Neurosci Res Grp, Szeged, Hungary
Bohar, Zsuzsanna
Martos, Diana
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Univ Szeged, Fac Med, Interdisciplinary Excellence Ctr, Albert Szent Gyorgyi Hlth Ctr,Dept Neurol, Szeged, HungaryMTA SZTE, Neurosci Res Grp, Szeged, Hungary
Martos, Diana
Telegdy, Gyula
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MTA SZTE, Neurosci Res Grp, Szeged, Hungary
Univ Szeged, Fac Med, Dept Pathophysiol, Szeged, HungaryMTA SZTE, Neurosci Res Grp, Szeged, Hungary
Telegdy, Gyula
Vecsei, Laszlo
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MTA SZTE, Neurosci Res Grp, Szeged, Hungary
Univ Szeged, Fac Med, Interdisciplinary Excellence Ctr, Albert Szent Gyorgyi Hlth Ctr,Dept Neurol, Szeged, HungaryMTA SZTE, Neurosci Res Grp, Szeged, Hungary