Chronic stress increases dopamine levels in hippocampal dentate gyrus and impairs spatial learning and memory in rats.
- Author:
Ke ZHAO
1
;
Peng REN
2
;
Ming-Yue LI
2
;
Qing-Hua JIN
2
;
Bin XIAO
3
Author Information
1. Department of Physiology, Baicheng Medical College, Baicheng 137000, China.
2. Department of Physiology and Pathophysiology, College of Medicine, Yanbian University, Yanji 133002, China.
3. Department of Physiology and Pathophysiology, College of Medicine, Yanbian University, Yanji 133002, China. xiaobin@ybu.edu.cn.
- Publication Type:Journal Article
- MeSH:
Animals;
Dentate Gyrus;
Dopamine;
Hippocampus;
Male;
Maze Learning;
Rats;
Rats, Sprague-Dawley;
Spatial Learning;
Spatial Memory
- From:
Acta Physiologica Sinica
2020;72(6):777-784
- CountryChina
- Language:Chinese
-
Abstract:
The objective of this study was to elucidate the effect of chronic stress (CS) on dopamine (DA) level and synaptic efficiency in the hippocampal dentate gyrus (DG) during spatial learning and memory. Sprague Dawley (SD) male rats were randomly divided into control group and CS group (n = 10). CS group was treated with chronic mild unpredictable stress, and control group did not receive any treatments. The levels of epinephrine and corticosterone (CORT) in serum were measured by using enzyme-linked immunosorbent assay (ELISA); the spatial learning and memory abilities of rats were measured by Morris water maze (MWM) test. Meanwhile, the amplitude of field excitatory postsynaptic potential (fEPSP) and concentration of DA in the DG region were determined by in vivo electrophysiology, microdialysis and HPLC techniques during MWM test in rats. After that, the DA D1 receptor (D1R) and its key downstream members in DG were examined by immunohistochemistry or Western blot assay. The results showed that the levels of epinephrine and CORT in the serum of the rats in CS group were significantly increased compared with those in the control group (P < 0.05). In CS group rats, the escape latency was significantly prolonged and the number of platform crossing was markedly decreased during MWM test, compared with those in control group (P < 0.05). Furthermore, the amplitude of fEPSP in the DG was not changed during MWM test in CS rats, while it was significantly increased on the 3rd day of MWM test in control group (P < 0.05). Compared with baseline or control group, CS group showed significantly increased DA level from the 1st to 3rd days of MWM test in the DG (P < 0.05). In addition, the protein expression of D1R was markedly up-regulated in the DG in CS group, while the protein expression levels of p-PKA, p-CREB and BDNF were significantly reduced, compared with those in control group. These results suggest that CS may impair spatial learning and memory abilities in rats through the enhancement of the DA levels in the hippocampal DG.
