Terminalia arjuna bark extract attenuates picrotoxin-induced behavioral changes by activation of serotonergic, dopaminergic, GABAergic and antioxidant systems.
10.1016/S1875-5364(17)30086-9
- Author:
Y CHANDRA SEKHAR
1
;
G PHANI KUMAR
2
;
K R ANILAKUMAR
1
Author Information
1. Applied Nutrition Division, Defence Food Research Laboratory, DRDO, Mysore-570011, Karnataka, India.
2. Applied Nutrition Division, Defence Food Research Laboratory, DRDO, Mysore-570011, Karnataka, India. Electronic address: phani_dfrl@rediffmail.com.
- Publication Type:Journal Article
- Keywords:
Anxiety;
Gene expression;
LC-MS;
Neurotransmitters;
Picrotoxin;
Terminalia arjuna
- MeSH:
Animals;
Antioxidants;
metabolism;
Anxiety Disorders;
drug therapy;
genetics;
metabolism;
psychology;
Brain-Derived Neurotrophic Factor;
genetics;
metabolism;
Dopamine Agents;
administration & dosage;
GABA Agents;
administration & dosage;
Glutathione Peroxidase;
genetics;
metabolism;
Humans;
Male;
Mice;
Mice, Inbred BALB C;
Neuronal Plasticity;
drug effects;
Neurotransmitter Agents;
metabolism;
Phytotherapy;
Picrotoxin;
adverse effects;
Plant Bark;
chemistry;
Plant Extracts;
administration & dosage;
Serotonin Agents;
administration & dosage;
Superoxide Dismutase-1;
genetics;
metabolism;
Terminalia;
chemistry
- From:
Chinese Journal of Natural Medicines (English Ed.)
2017;15(8):584-596
- CountryChina
- Language:English
-
Abstract:
Stress and emotion are associated with several illnesses from headaches to heart diseases and immune deficiencies to central nervous system. Terminalia arjuna has been referred as traditional Indian medicine for several ailments. The present study aimed to elucidate the effect of T. arjuna bark extract (TA) against picrotoxin-induced anxiety. Forty two male Balb/c mice were randomly divided into six experimental groups (n = 7): control, diazepam (1.5 mg·kg), picrotoxin (1 mg·kg) and three TA treatemt groups (25, 50, and 100 mg/kg). Behavioral paradigms and PCR studies were performed to determine the effect of TA against picrotoxin-induced anxiety. The results showed that TA supplementation increased locomotion towards open arm (EPM) and illuminated area (light-dark box test), and increased rearing frequency (open field test) in a dose dependent manner, compared to picrotoxin (P < 0.05). Furthermore, TA increased number of licks and shocks in Vogel's conflict. PCR studies showed an up-regulation of several genes, such as BDNF, IP, DL, CREB, GABA, SOD, GPx, and GR in TA administered groups. In conclusion, alcoholic extract of TA bark showed protective activity against picrotoxin in mice by modulation of genes related to synaptic plasticity, neurotransmitters, and antioxidant enzymes.
