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The extracts of Fructus Akebiae, a preparation containing 90% of the active ingredient hederagenin: serotonin, norepinephrine and dopamine reuptake inhibitor.
- Source :
-
Pharmacology, biochemistry, and behavior [Pharmacol Biochem Behav] 2012 Jan; Vol. 100 (3), pp. 431-9. Date of Electronic Publication: 2011 Oct 08. - Publication Year :
- 2012
-
Abstract
- Fructus Akebiae is a traditional Chinese herbal extract that has been used for the treatment of depressive disorders in China. Previous studies demonstrated that Fructus Akebiae extracts (FAE) displayed a potent antidepressant-like activity in animal behavior tests and found that the specific active ingredient from the extracts of Fructus Akebiae is hederagenin. However, the underlying mechanism is unknown. Here we provide evidences that FAE enhances the signaling of central monoamines via inhibition of the reuptake of the extracellular monoamines including serotonin (5-HT), norepinephrine (NE) and dopamine (DA). In rat brain membrane preparations and HEK293 cells transfected with human serotonin transporter (SERT), NE transporter (NET) and DA transporter (DAT), we found that FAE displayed marked affinity to rat and cloned human monoamine transporters in ex vivo and in vitro experiments, using competitive radio ligand binding assay. In uptake assays using rat synaptosomes and transfected cells, FAE was found to significantly inhibit all three monoamine transporters in a dose- and time-dependent manner, with a comparable or better potency to their corresponding specific inhibitors. In contrast, FAE (10 μM), showed no significant affinity to a variety array of receptors tested from CNS. In support of our uptake data, in vivo microdialysis studies showed that administration of FAE (12.6, 25, 50 mg/kg) significantly increased extracellular concentrations of 5-HT, NE and DA in frontal cortex of freely moving rats. Taken together, our current study showed for the first time that FAE is a novel triple inhibitor of monoamine transporters, which may be one the mechanisms of its antidepressant activity.<br /> (Copyright © 2011 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Biogenic Monoamines metabolism
Dopamine Plasma Membrane Transport Proteins antagonists & inhibitors
Dopamine Plasma Membrane Transport Proteins genetics
Dopamine Plasma Membrane Transport Proteins metabolism
Dose-Response Relationship, Drug
Drugs, Chinese Herbal chemistry
Frontal Lobe drug effects
Frontal Lobe metabolism
HEK293 Cells
Humans
Male
Nerve Tissue Proteins antagonists & inhibitors
Nerve Tissue Proteins genetics
Nerve Tissue Proteins metabolism
Norepinephrine Plasma Membrane Transport Proteins antagonists & inhibitors
Norepinephrine Plasma Membrane Transport Proteins genetics
Norepinephrine Plasma Membrane Transport Proteins metabolism
Oleanolic Acid analysis
Oleanolic Acid pharmacology
Rats
Rats, Sprague-Dawley
Recombinant Proteins antagonists & inhibitors
Recombinant Proteins genetics
Recombinant Proteins metabolism
Serotonin Plasma Membrane Transport Proteins chemistry
Serotonin Plasma Membrane Transport Proteins genetics
Serotonin Plasma Membrane Transport Proteins metabolism
Synaptosomes metabolism
Up-Regulation drug effects
Brain drug effects
Drugs, Chinese Herbal pharmacology
Neurons drug effects
Neurotransmitter Uptake Inhibitors pharmacology
Oleanolic Acid analogs & derivatives
Synaptosomes drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1873-5177
- Volume :
- 100
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Pharmacology, biochemistry, and behavior
- Publication Type :
- Academic Journal
- Accession number :
- 22005599
- Full Text :
- https://doi.org/10.1016/j.pbb.2011.10.001