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Neurological mechanism of Xiaochaihutang's antidepressant-like effects to socially isolated adult rats
被引:25
作者:
Ma, Jie
[1
]
Wu, Chun Fu
[1
]
Wang, Fang
[1
]
Yang, Jing Yu
[1
]
Dong, Ying Xu
[1
]
Su, Guang Yue
[2
]
Zhang, Kuo
[1
]
Wang, Zhi Qian
[1
]
Xu, Long Wen
[1
]
Pan, Xing
[1
]
Zhou, Ting Shuo
[1
]
Ma, Ping
[1
]
Song, Shao Jiang
[3
]
机构:
[1] Shenyang Pharmaceut Univ, Dept Pharmacol, Box 31,103 Wenhua Rd, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Dept Funct Food & Wine, Shenyang, Peoples R China
[3] Shenyang Pharmaceut Univ, Dept Tradit Chinese Mat Med, Shenyang, Peoples R China
基金:
中国国家自然科学基金;
关键词:
5-HT1A receptor;
chronic social isolation stress;
neurogenesis;
neurotransmitter;
DEPRESSIVE-LIKE BEHAVIOR;
HIPPOCAMPAL NEUROGENESIS;
EXPRESSION;
SEROTONIN;
STRESS;
MODEL;
5-HT1A;
MICE;
CONSTITUENTS;
NEUROBIOLOGY;
D O I:
10.1111/jphp.12616
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Objectives Xiaochaihutang (XCHT) has antidepressant effects in multiple animal models of depression in our previous studies. But the antidepressant effects and exact mechanisms of XCHT in a rat model of chronic social isolation stress (CSIS) have never been studied. We therefore aimed to investigate the effects of XCHT on depressive/anxiety-related behaviours of CSIS-exposed rats and understand the neurological mechanism involving neurogenesis. Methods We established the CSIS model and then investigated the effects of XCHT on behavioural change. HPLC-MS/MS was adopted to quantify neurotransmitter levels in the cerebrospinal fluid (CSF). Immunofluorescence technology was used to study the effects of XCHT on neurogenesis; while expressions of 5-HT1A receptor signalling pathway in the hippocampus were measured using Western blotting. Key Findings Xiaochaihutang significantly alleviated depressive/anxiety-like behaviours of CSIS-exposed rats. XCHT significantly regulated levels of monoamine neurotransmitters in the CSF without affecting Glu, GABA and ACh. XCHT also significantly increased neurogenesis in CSIS-exposed rats. Additionally, XCHT reversed CSIS-induced decrease of 5-HT1A receptor expression and promoted the expression of BDNF in the hippocampus. Conclusion Our results suggest that XCHT could significantly regulate the depressive/anxiety-like behaviours induced by CSIS, which are likely attributed to the promotion of hippocampal neurogenesis and neurotrophin expressions through the activation of serotonergic system.
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页码:1340 / 1349
页数:10
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