Antidepressant mechanism of Shenling Kaixin Granules based on BDNF/TrkB/CREB pathway.
10.19540/j.cnki.cjcmm.20221114.402
- Author:
Yan XU
1
;
Dong-Guang LIU
1
;
Ting-Bo NING
1
;
Jian-Guo ZHU
1
;
Ru YAO
1
;
Xue MENG
1
;
Jing-Chun YAO
1
;
Wen-Xue ZHAO
1
Author Information
1. New Drug Pharmacological Center of Lunan Pharmaceutical Group Corporation Linyi 276006, China State Key Laboratory of Generic Manufacture Technology of Chinese Traditional Medicine Linyi 276006, China.
- Publication Type:Journal Article
- Keywords:
BDNF/TrkB/CREB pathway;
Nrf2/HO-1 pathway;
Shenling Kaixin Granules;
caspase-3 pathway;
chronic unpredictable mild stress(CUMS);
depression
- MeSH:
Rats;
Male;
Animals;
bcl-2-Associated X Protein/metabolism*;
Caspase 3/metabolism*;
Nerve Growth Factor/metabolism*;
Brain-Derived Neurotrophic Factor/metabolism*;
Signal Transduction;
Tumor Necrosis Factor-alpha/metabolism*;
Serotonin/metabolism*;
NF-E2-Related Factor 2/metabolism*;
Rats, Sprague-Dawley;
Antidepressive Agents/pharmacology*;
Hippocampus/metabolism*;
Superoxide Dismutase/metabolism*;
Sugars/pharmacology*;
Depression/genetics*;
Stress, Psychological/metabolism*
- From:
China Journal of Chinese Materia Medica
2023;48(8):2184-2192
- CountryChina
- Language:Chinese
-
Abstract:
To investigate the antidepressant mechanism of Shenling Kaixin Granules(SLKX) in treating chronic unpredictable mild stress(CUMS) model rats. Ninety male SD rats were randomly divided into control group, model group, Shugan Jieyu Capsules(110 mg·kg~(-1)) group and SLKX low-(90 mg·kg~(-1)), medium-(180 mg·kg~(-1)), and high-dose(360 mg·kg~(-1)) groups. Depression rat model was replicated by CUMS method. After treatment, the behavioral changes of rats were evaluated by sugar preference, open field, elevated cross maze and forced swimming experiments. The contents of interleukin 1 beta(IL-1β), tumor necrosis factor α(TNF-α), brain-derived neurotrophic factor(BDNF) and 5-hydroxytryptamine(5-HT) in serum were determined by enzyme linked immunosorbent assay(ELISA), and the activities of superoxide dismutase(SOD) and catalase(CAT) in hippocampal CA1 region were also detected. Pathological changes in hippocampal CA1 region were detected by hematoxylin-eosin(HE) staining, and Western blot was used to determine the expression of nerve growth factor(NGF), BDNF, phospho-tyrosine kinase receptor(p-TrkB)/TrkB, phospho-cAMP-response element binding protein(p-CREB)/CREB, nuclear factor E2 related factor 2(Nrf2), heme oxygenase 1(HO-1), B-cell lymphoma-2(Bcl-2)/Bcl-2 associated X protein(Bax) and caspase-3 in hippocampal CA1 region. RESULTS:: showed that compared with the control group, the model group had decreased sugar preference, reduced number of entries and time spent in the center of open field and shortened total distance of movement, reduced number of entries and proportion of time spent in open arm, and increased number and time of immobility in forced swimming experiment. Additionally, the serum contents of IL-1β and TNF-α and the expression of caspase-3 were higher, while the contents of BDNF and 5-HT, the activities of SOD and CAT in hippocampal CA1 region, the expressions of NGF, BDNF, p-TrkB/TrkB, p-CREB/CREB, HO-1 and Bcl-2/Bax, and the Nrf2 nuclear translocation were lower in model group than in control group. Compared with the conditions in model group, the sugar preference, the number of entries and time spent in the center of open, total distance of movement, and the number of entries and proportion of time spent in open arm in treatment groups were increased while the number and time of immobility in forced swimming experiment were decreased; the serum contents of IL-1β and TNF-α and the expression of caspase-3 were down regulated, while the contents of BDNF and 5-HT, the activities of SOD and CAT in hippocampal CA1 region, the expressions of NGF, BDNF, p-TrkB/TrkB, p-CREB/CREB, HO-1, Bcl-2/Bax, and Nrf2 nuclear translocation were enhanced. In conclusion, SLKX might regulate the Nrf2 nucleus translocation by activating BDNF/TrkB/CREB pathway, lower oxidative stress damage in hippocampus, inhibit caspase-3 activity, and reduce apoptosis of hippocampal nerve cells, thereby playing an antidepressant role.
