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Low corticosterone levels attenuate late life depression and enhance glutamatergic neurotransmission in female rats

Shi-feng Chu1, Zhao Zhang1, Xin Zhou1, Wen-bin He2, Bo Yang3, Li-yuan Cui1, Hong-yuan He4, Zhen-zhen Wang1, Nai-hong Chen1
1 State Key Laboratory of Bioactive Substances and Functions of Natural Medicines, Institute of Materia Medica and Neuroscience Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
2 Shanxi Key Laboratory of Chinese Medicine Encephalopathy, Shanxi University of Chinese Medicine, Jinzhong 030619, China
3 Department of Pharmacy, Characteristic Medical Center of the Chinese People’s Armed Police Force, Tianjin 300300, China
4 Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China
Correspondence to: Nai-hong Chen: chennh@imm.ac.cn,
DOI: 10.1038/s41401-020-00536-w
Received: 18 April 2020
Accepted: 11 September 2020
Advance online: 7 October 2020

Abstract

Sustained elevation of corticosterone (CORT) is one of the common causes of aging and major depression disorder. However, the role of elevated CORT in late life depression (LLD) has not been elucidated. In this study, 18-month-old female rats were subjected to bilateral adrenalectomy or sham surgery. Their CORT levels in plasma were adjusted by CORT replacement and the rats were divided into high-level CORT (H-CORT), low-level CORT (L-CORT), and Sham group. We showed that L-CORT rats displayed attenuated depressive symptoms and memory defects in behavioral tests as compared with Sham or H-CORT rats. Furthermore, we showed that glutamatergic transmission was enhanced in L-CORT rats, evidenced by enhanced population spike amplitude (PSA) recorded from the dentate gyrus of hippocampus in vivo and increased glutamate release from hippocampal synaptosomes caused by high frequency stimulation or CORT exposure. Intracerebroventricular injection of an enzymatic glutamate scavenger system, glutamic-pyruvic transmine (GPT, 1 μM), significantly increased the PSA in Sham rats, suggesting that extracelluar accumulation of glutamate might be the culprit of impaired glutamatergic transmission, which was dependent on the uptake by Glt-1 in astrocytes. We revealed that hippocampal Glt-1 expression level in the L-CORT rats was much higher than in Sham and H-CORT rats. In a gradient neuron–astrocyte coculture, we found that the expression of Glt-1 was decreased with the increase of neural percentage, suggesting that impairment of Glt-1 might result from the high level of CORT contributed neural damage. In sham rats, administration of DHK that inhibited Glt-1 activity induced significant LLD symptoms, whereas administration of RIL that promoted glutamate uptake significantly attenuated LLD. All of these results suggest that glutamatergic transmission impairment is one of important pathogenesis in LLD induced by high level of CORT, which provide promising clues for the treatment of LLD.
Keywords: major depression disorder; late life depression; corticosterone; hippocampus; glutamatergic transmission; glutamate/ glutamine cycle; glutamate transporter 1

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