期刊论文详细信息
BMC Gastroenterology
Psychological stress induced zinc accumulation and up-regulation of ZIP14 and metallothionein in rat liver
Hui Shen1  Jianxin Qian2  Xiao Dou1  Liping Tao1  Zhilei Shen1  Yingjie Li1  Yuanyuan Zheng3  Xue Tian1 
[1] Department of Naval Hygiene, Second Military Medical University, 800 Xiangyin Road, Shanghai 200433, PR China;Department of Medical Oncology, Changzheng Hospital, No. 64 Hetian Road, Shanghai 200070, China;Department of Immunology, Second Military Medical University, No. 800 Xiangyin Road, Shanghai 200433, China
关键词: Corticosterone;    Liver;    Metallothionein;    ZIP14;    Zinc;    Psychological stress;   
Others  :  855707
DOI  :  10.1186/1471-230X-14-32
 received in 2013-05-03, accepted in 2014-02-13,  发布年份 2014
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【 摘 要 】

Background

Zinc is necessary for normal liver function; and vice versa, the liver plays a central role in zinc homeostasis. The aim of present study is to assess the effects of repeated psychological stress (PS) on the zinc metabolism and related mechanism involved in zinc homeostasis in rat liver.

Methods

In present study, we used communication box to create PS model and investigated the serum corticosterone (CORT), zinc level in serum and liver, liver metallothionein (MT) content and ZRT/IRT-like Protein 14 (ZIP14) mRNA expression.

Results

The results showed that the serum CORT level increased and serum zinc level decreased significantly after 7 d and 14 d PS treatment. Meanwhile, zinc and MT contents in liver were elevated after 14 d PS exposure, while those in 7 d PS exposure group did not change. ZIP14 mRNA was expressed markedly at 7 d after the onset of PS, while Zip14 mRNA expression in the liver after 14 d PS exposure reached normal level compared with control group.

Conclusions

The results suggest that PS exposure could induce hypozincemia, which might be related to liver zinc accumulation because of high level of MT through glucocorticoid-mediated MT synthesis and ZIP14 expression induced by interleukin-6.

【 授权许可】

   
2014 Tian et al.; licensee BioMed Central Ltd.

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