Shuyang Ji

Shuyang Ji

orcid

Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 February 2025 in Supportive Care in Cancer
Verified
Journal Article
Closed access
PDF file
YLYang Li
Yang Li
SJShuyang Ji
Shuyang Ji
YTYanmin Tao
Yanmin Tao
HWHongyan Wang
Hongyan Wang
ZWZhifei Wen
Zhifei Wen
XZXiangeng Zhang
Xiangeng Zhang

22 May 2024 in Journal of the American Medical Directors Association
Verified
Journal Article
Closed access
YTYan Min Tao
Yan Min Tao
HWHongyan Wang
Hongyan Wang
JLJingsong Luo
Jingsong Luo
HZHong Zhang
Hong Zhang
WZWen Zhang
Wen Zhang
XZXiangeng Zhang
Xiangeng Zhang

7 June 2025 in Archives of Gerontology and Geriatrics
Verified
Journal Article
Closed access
DYDongmei Yao
Dongmei Yao
SYShenbi Yang
Shenbi Yang
ZWZhifei Wen
Zhifei Wen
JHJing He
Jing He
SJShuyang Ji
Shuyang Ji
XZXiangeng Zhang
Xiangeng Zhang

23 April 2025 in Scientific Reports
Verified
Journal Article
Open access
PDF file
HWHongyan Wang
Hongyan Wang
QLQingfang Liang
Qingfang Liang
ZWZhifei Wen
Zhifei Wen
WMWenlian Ma
Wenlian Ma
SJShuyang Ji
Shuyang Ji
XZXiangeng Zhang
Xiangeng Zhang
Depression is a serious and common complication of diabetes, with a well-established link between the two conditions. Recent studies indicate that activation of the NLRP3 inflammasome in hippocampal microglia plays a key role in the pathogenesis of diabetes complicated with depression (DD). While environmental enrichment (EE) has demonstrated significant anti-neuroinflammatory effects, its potential to alleviate neuroinflammation specifically induced by DD remains unclear. The DD rat model was established using a combination of a high-fat diet, streptozotocin injection, and chronic unpredictable mild stress. The effects of EE on NLRP3 inflammasome activation in the hippocampal microglia of DD rats were examined through a series of behavioral tests (open field test, forced swim test, and elevated plus maze), along with enzyme-linked immunosorbent assays, hematoxylin and eosin staining, TdT-mediated dUTP nick-end labeling staining, Western blot analysis, and immunofluorescence. Compared to the control group, DD rats exhibited impaired glucose metabolism and increased depressive-like behaviors, alongside hippocampal neuronal damage and elevated apoptosis rates. Activation of the NLRP3 inflammasome in hippocampal microglia was observed, with upregulation of the NLRP3 signaling pathway and inhibition of the PI3K/AKT signaling pathway. EE significantly mitigated these effects, reducing hippocampal neuroinflammation and alleviating depressive behaviors in DD rats. Neuroinflammation in the hippocampus is a key mechanism underlying the pathogenesis of DD. This study demonstrated that EE reduces neuroinflammation, likely by inhibiting the activation of the NLRP3 inflammasome in hippocampal microglia.