Chunmei Li

Dr. Chunmei Li

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

View All Publications
1 August 2019 in Environmental Pollution
Verified
Journal Article
Closed access
RKRuifen Kang
Ruifen Kang
RLRuonan Li
Ruonan Li
PDPengyuan Dai
Pengyuan Dai
ZLZhaojian Li
Zhaojian Li
YLYansen Li
Yansen Li
Chunmei LiChunmei Li
Chunmei Li

1 June 2020 in Environmental Pollution
Verified
Journal Article
Closed access
QTQian Tang
Qian Tang
JTJuan Tang
Juan Tang
XRXin Ren
Xin Ren
Chunmei LiChunmei Li
Chunmei Li

1 December 2018 in Environmental Pollution
Verified
Journal Article
Closed access
XRXin Ren
Xin Ren
RLRuonan Li
Ruonan Li
JLJunze Liu
Junze Liu
KHKai Huang
Kai Huang
SWSheng Wu
Sheng Wu
Chunmei LiChunmei Li
Chunmei Li

1 June 2016 in Acta Histochemica
Verified
Journal Article
Closed access
PDPengyuan Dai
Pengyuan Dai
PHPing Hu
Ping Hu
JTJuan Tang
Juan Tang
YLYansen Li
Yansen Li
Chunmei LiChunmei Li
Chunmei Li

1 January 2013 in Reproductive Biology and Endocrinology
Verified
Journal Article
Open access
PDF file
YLYansen Li
Yansen Li
YHYi Huang
Yi Huang
YPYuanguo Piao
Yuanguo Piao
KNKentaro Nagaoka
Kentaro Nagaoka
GWGen Watanabe
Gen Watanabe
Chunmei LiChunmei Li
Chunmei Li
Whole body heat stress had detrimental effect on male reproductive function. It's known that the nuclear factor erythroid 2-related factor 2 (Nrf2) activates expression of cytoprotective genes to enable cell adaptation to protect against oxidative stress. However, it’s still unclear about the exactly effects of Nrf2 on the testis. Here, we investigate the protective effect of Nrf2 on whole body heat stress-induced oxidative damage in mouse testis.

19 December 2017 in Frontiers in Physiology
Verified
Journal Article
Open access
JTJuan Tang
Juan Tang
PHPing Hu
Ping Hu
YLYansen Li
Yansen Li
TWTin-Tin Win-Shwe
Tin-Tin Win-Shwe
Chunmei LiChunmei Li
Chunmei Li
Glyphosate (N-phosphonomethyl-glycine, GLP) is the most popular herbicide used worldwide. This study aimed to investigate the effects of glyphosate on rats' liver function and induction of pathological changes in ion levels and oxidative stress in hepatic tissue. Sprague-Dawley rats were treated orally with 0, 5, 50, and 500 mg/kg body weight of the GLP. After 5 weeks of treatment, blood and liver samples were analyzed for biochemical and histomorphological parameters. The various mineral elements content in the organs of the rats were also measured. Significant decreases were shown in the weights of body, liver, kidney and spleen between the control and treatment groups. Changes also happened in the histomorphology of the liver and kidney tissue of GLP-treated rats. The GLP resulted in an elevated level of glutamic-oxalacetic transaminase (GOT), glutamic-pyruvic transaminase (GPT) and IL-1β in the serum. Besides, decreased total superoxide dismutase (T-SOD) activity and increased malondialdehyde (MDA) contents in the serum, liver, and kidney indicated the presence of oxidative stress. Moreover, increase of hydrogen peroxide (H2O2) level and catalase (CAT) activity in the serum and liver and decrease of glutathione (GSH) and lutathione peroxidase (GSH-Px) activity in the kidney tissue further confirmed the occurrence of oxidative stress. The results of RT-PCR showed that the mRNA expressions of IL-1α, IL-1β, IL-6, MAPK3, NF-κB, SIRT1, TNF-α, Keap1, GPX2, and Caspase-3 were significantly increased in the GLP-treated groups compared to the control group. Furthermore, PPARα, DGAT, SREBP1c, and SCD1 mRNA expressions were also remarkably increased in the GLP-treated groups compared to the control group. In addition, aluminum (Al), iron (Fe), copper (Cu), zinc (Zn), and magnesium (Mg) levels were showed a significant difference reduction or increase in rat liver, kidney, spleen, lung, heart, muscle, brain, and fat tissues. These results suggested that glyphosate caused obvious damage to rats' liver and caused various mineral elements content imbalances in various organs of rats. Ion imbalance could weaken antioxidant capacity and involve in the mechanism of liver oxidative damage caused by GLP.