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Potentiation of Antidepressant Effects of Agomelatine and Bupropion by Hesperidin in Mice
- Source :
- Neurology Research International, Vol 2018 (2018), Neurology Research International
- Publication Year :
- 2018
- Publisher :
- Hindawi, 2018.
-
Abstract
- Hesperidin, a well-known flavanone glycoside mostly found in citrus fruits, showed neuroprotective and antidepressant activity. Agomelatine, a melatonergic MT1/MT2 agonist and 5-HT2C receptor antagonist, exhibits good antidepressant efficacy. Bupropion has been widely used for the treatment of depression because of its dopamine and norepinephrine reuptake inhibition. The objective of present study was to assess the antidepressant effects of hesperidin combination with agomelatine or bupropion. Male Swiss Albino mice received treatment of saline, vehicle, ‘hesperidin alone’, ‘agomelatine alone’, hesperidin+agomelatine, ‘bupropion alone’, hesperidin+bupropion, and agomelatine+bupropion for 14 days. The immobility period was analysed 30 min after the treatment in forced swim and tail suspension tests. Dopamine and serotonin levels were analysed in hippocampus, cerebral cortex, and whole brain using HPLC with fluorescence detector. Hesperidin plus agomelatine treated group was better in terms of decrease in immobility period and increase in dopamine and serotonin levels when compared to their respective monotherapy treated groups.
- Subjects :
- Agonist
Article Subject
medicine.drug_class
Pharmacology
lcsh:RC346-429
03 medical and health sciences
Hesperidin
chemistry.chemical_compound
0302 clinical medicine
Dopamine
medicine
Agomelatine
lcsh:Neurology. Diseases of the nervous system
Bupropion
business.industry
Receptor antagonist
030227 psychiatry
Neurology
chemistry
Antidepressant
Neurology (clinical)
Serotonin
business
030217 neurology & neurosurgery
Research Article
medicine.drug
Subjects
Details
- Language :
- English
- ISSN :
- 20901852
- Database :
- OpenAIRE
- Journal :
- Neurology Research International
- Accession number :
- edsair.doi.dedup.....170a71bc155624217f75f6d0e750f2aa
- Full Text :
- https://doi.org/10.1155/2018/9828639