Your browser doesn't support javascript.
loading
Cytisine, a Partial Agonist of α4β2 Nicotinic Acetylcholine Receptors, Reduced Unpredictable Chronic Mild Stress-Induced Depression-Like Behaviors
Biomolecules & Therapeutics ; : 291-297, 2016.
Article in English | WPRIM | ID: wpr-51944
ABSTRACT
Cytisine (CYT), a partial agonist of α4β2-nicotinic receptors, has been used for antidepressant efficacy in several tests. Nicotinic receptors have been shown to be closely associated with depression. However, little is known about the effects of CYT on the depression. In the present study, a mouse model of depression, the unpredictable chronic mild stress (UCMS), was used to evaluate the activities of CYT. UCMS caused significant depression-like behaviors, as shown by the decrease of total distances in open field test, and the prolonged duration of immobility in tail suspension test and forced swimming test. Treatment with CYT for two weeks notably relieved the depression-like behaviors in the UCMS mice. Next, proteins related to depressive disorder in the brain region of hippocampus and amygdala were analyzed to elucidate the underlying mechanisms of CYT. CYT significantly reversed the decreases of 5-HT1A, BDNF, and mTOR levels in the hippocampus and amygdala. These results imply that CYT may act as a potential anti-depressant in the animals under chronic stress.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Brain / Receptors, Nicotinic / Brain-Derived Neurotrophic Factor / Hindlimb Suspension / Depression / Depressive Disorder / Physical Exertion / Hippocampus / Amygdala Type of study: Prognostic study Limits: Animals Language: English Journal: Biomolecules & Therapeutics Year: 2016 Type: Article

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: WPRIM (Western Pacific) Main subject: Brain / Receptors, Nicotinic / Brain-Derived Neurotrophic Factor / Hindlimb Suspension / Depression / Depressive Disorder / Physical Exertion / Hippocampus / Amygdala Type of study: Prognostic study Limits: Animals Language: English Journal: Biomolecules & Therapeutics Year: 2016 Type: Article