Siping Wei

Prof. Dr. Siping Wei

orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

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

Representative Publications

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22 August 2024 in Journal of Colloid and Interface Science
Verified
Journal Article
Closed access
HZHaibo Zhou
Haibo Zhou
KWKaili Wu
Kaili Wu
XLXunwen Luo
Xunwen Luo
QCQinghong Cai
Qinghong Cai
JZJia Zeng
Jia Zeng
SWSiping Wei
Siping Wei

1 March 2021 in Advanced Synthesis & Catalysis
Verified
Journal Article
Closed access
PDF file
MZMin Zhang
Min Zhang
ZZZhijie Zhang
Zhijie Zhang
YHYangsen He
Yangsen He
TZTing Zou
Ting Zou
ZQZhongyu Qi
Zhongyu Qi
DYDong Yi
Dong Yi

4 February 2022 in Chemical Communications
Verified
Journal Article
Closed access
PDF file
HLHao Li
Hao Li
YHYishu He
Yishu He
DZDi Zhang
Di Zhang
LYLi Yang
Li Yang
JZJiarui Zhang
Jiarui Zhang
QFQifeng Fu
Qifeng Fu
We describe a photocatalytic [2+2] cycloaddition of redox-sensitive aliphatic-amine-containing indole derivatives assisted by a hydrogen bond, which affords a range of cyclobutane-fused polycyclic indoline derivatives, especially bridged-cyclic indolines.

10 November 2020 in Chinese Journal of Chemistry
Verified
Journal Article
Closed access
PDF file
DYDong Yi
Dong Yi
LHLinying He
Linying He
ZQZhongyu Qi
Zhongyu Qi
ZZZhijie Zhang
Zhijie Zhang
MLMengshun Li
Mengshun Li
SWSiping Wei
Siping Wei

21 February 2025 in Journal of Hazardous Materials
Verified
Journal Article
Closed access
KWKaili Wu
Kaili Wu
YTYacen Tang
Yacen Tang
YQYirui Qiu
Yirui Qiu
HZHaibo Zhou
Haibo Zhou
XLXingyan Liu
Xingyan Liu
FDFan Dong
Fan Dong

18 October 2024 in Frontiers in Pharmacology
Verified
Journal Article
Open access
PDF file
QRQingyi Ren
Qingyi Ren
CHChenxi He
Chenxi He
YSYuhong Sun
Yuhong Sun
XGXiaowei Gao
Xiaowei Gao
YZYan Zhou
Yan Zhou
FWFang Wang
Fang Wang
Background: Asiaticoside, the main active ingredient of Centella asiatica, is a pentacyclic triterpenoid compound. Previous studies have suggested that asiaticoside possesses neuroprotective and anti-depressive properties, however, the mechanism of its anti-depressant action not fully understood. In recent years, a growing body of research on anti-depressants has focused on the microbiota-gut-brain axis, we noted that disruption of the gut microbial community structure and diversity can induce or exacerbate depression, which plays a key role in the regulation of depression.Methods: Behavioral experiments were conducted to detect depression-like behavior in mice through sucrose preference, forced swimming, and open field tests. Additionally, gut microbial composition and short-chain fatty acid (SCFA) levels in mouse feces were analyzed 16S rRNA sequencing and gas chromatography-mass spectrometry (GC-MS). Hippocampal brain-derived neurotrophic factor (BDNF) and 5-hydroxytryptamine receptor 1A (5-HT1A) expression in mice was assessed by western blotting. Changes in serum levels of inflammatory factors, neurotransmitters, and hormones were measured in mice using ELISA.Results: This study revealed that oral administration of asiaticoside significantly improved depression-like behavior in chronic unpredictable mild stress (CUMS) mice. It partially restored the gut microbial community structure in CUMS mice, altered SCFA metabolism, regulated the hypothalamic–pituitary–adrenal axis (HPA axis) and inflammatory factor levels, upregulated BDNF and 5-HT1A receptor protein expression, and increased serum serotonin (5-hydroxytryptamine, 5-HT) concentration. These findings reveal that asiaticoside exerts antidepressant effects via the microbiota-gut-brain axis.Conclusions: These results suggested that asiaticoside exerts antidepressant effects through the microbiota-gut-brain axis in a CUMS mouse model.