Showing posts with label mRNA expression. Show all posts
Showing posts with label mRNA expression. Show all posts

Monday, 2 February 2026

Hepatoprotective Effects of Liubao Tea Polyphenols against CCl₄-Induced Liver Injury in Mice via Antioxidant Activity | Chapter 7 | Molecular Mechanisms and Signaling Pathways of the Anti-inflammatory Effects of Functional Foods

Active oxygen free radicals cause oxidative stress, which is a common pathophysiological mechanism of liver diseases. Tea polyphenols can sequester lipid peroxidation free radicals during the peroxidation process, lower polyphenolic free-radical content, and interrupt free-radical oxidation chain reactions, thereby effectively removing free radicals. This study investigated the protective effect of Liubao tea polyphenols (PLT) against carbon tetrachloride (CCl₄)-induced liver injury in mice. Mice were pretreated with PLT prior to the administration of CCl₄ (10 mL/kg) to induce hepatic damage. Subsequently, liver and serum biochemical parameters, along with the expression levels of relevant messenger RNAs (mRNAs) and proteins in liver tissue, were assessed. The results demonstrated that PLT administration significantly ameliorated liver injury, as indicated by reduced liver indices and improved histological architecture. Specifically, PLT downregulated serum levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), triglycerides (TGs), and malondialdehyde (MDA), while elevating the activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px). Furthermore, PLT decreased the serum concentrations of pro-inflammatory cytokines, including interleukin-6 (IL-6), IL-12, tumour necrosis factor-α (TNF-α), and interferon-γ (IFN-γ). Histopathological examination revealed that PLT attenuated CCl₄-induced central venous alterations and hepatocellular damage. At the molecular level, quantitative PCR and Western blot analyses confirmed that PLT upregulated the mRNA and protein expression of antioxidant enzymes—Cu/Zn-SOD, Mn-SOD, catalase (CAT), and GSH-Px—as well as the NF-κB inhibitor IκB-α in liver tissues. Conversely, PLT downregulated the expression of cyclooxygenase-2 (COX-2) and nuclear factor kappa B (NF-κB). Additionally, PLT increased the protein levels of phosphorylated NF-κB p65 (p-NF-κB p65) and cytochrome P450 reductase in injured livers. PLT comprises several bioactive compounds, such as gallic acid, catechin, caffeine, epicatechin (EC), epigallocatechin gallate (EGCG), gallocatechin gallate (GCG), and epicatechin gallate (ECG), which may contribute to its broad biological activities. In conclusion, PLT exerts a preventive effect against CCl₄-induced liver injury, comparable to that of silymarin, likely through the modulation of oxidative stress and inflammatory pathways. In this study, toxic carbon tetrachloride was used to simulate chemical-induced liver injury, and the observed effects remained at the laboratory level. In order to better prove this study’s argument, future research on the human body is expected. The role of PLT in liver injury needs to be further studied, which will be conducive to more obvious discoveries of the link between its active components and their mechanisms. At the same time, in view of the mechanism of PLT, it is necessary to verify the mechanism more accurately for the differences across PLT components in the future.

 

 

Author(s) Details

Yanni Pan
Chongqing Collaborative Innovation Center for Functional Food, Chongqing University of Education, Chongqing 400067, China, Chongqing Engineering Research Center of Functional Food, Chongqing University of Education, Chongqing 400067, China, Chongqing Engineering Laboratory for Research and Development of Functional Food, Chongqing University of Education, Chongqing 400067, China, College of Biological and Chemical Engineering, Chongqing University of Education, Chongqing 400067, China and Department of Food Science and Biotechnology, Cha University, Gyeongghi-do 487-010, South Korea.

 

Xingyao Long
Chongqing Collaborative Innovation Center for Functional Food, Chongqing University of Education, Chongqing 400067, China, Chongqing Engineering Research Center of Functional Food, Chongqing University of Education, Chongqing 400067, China, Chongqing Engineering Laboratory for Research and Development of Functional Food, Chongqing University of Education, Chongqing 400067, China and College of Biological and Chemical Engineering, Chongqing University of Education, Chongqing 400067, China.

 

Ruokun Yi
Chongqing Collaborative Innovation Center for Functional Food, Chongqing University of Education, Chongqing 400067, China, Chongqing Engineering Research Center of Functional Food, Chongqing University of Education, Chongqing 400067, China and Chongqing Engineering Laboratory for Research and Development of Functional Food, Chongqing University of Education, Chongqing 400067, China.

 

Xin Zhao
Chongqing Collaborative Innovation Center for Functional Food, Chongqing University of Education, Chongqing 400067, China, Chongqing Engineering Research Center of Functional Food, Chongqing University of Education, Chongqing 400067, China and Chongqing Engineering Laboratory for Research and Development of Functional Food, Chongqing University of Education, Chongqing 400067, China.

 

Please see the book here :- https://doi.org/10.9734/bpi/mono/978-81-998509-0-3/CH7

Wednesday, 6 December 2023

Effects of Refined Xiaoyaosan on Depressive-Like Behaviors in Rats with Chronic Unpredictable Mild Stress through Neurosteroids, their Synthesis and Metabolic Enzymes | Chapter 11 | Insights into the Prevention and Treatment of Depression with Famous TCM Prescription Xiaoyaosan

 To observe the effects of refined Xiaoyaosan (XYS) on the depressive-like behaviors in rats with chronic unpredictable mild stress (CUMS), and to explore the relationship between the changes of neurosteroids and mRNA expressions of their synthesis and metabolic enzymes, and the mechanism of XYS in the treatment of depression. Methods: Eighty-four healthy male Sprague-Dawley rats were randomly divided into normal group, model group, XYS group and fluoxetine group. The latter three groups were subjected to 21 days of CUMS to prepare the stress depression model. Rats in the XYS group, and fluoxetine group were given intragastric administration with refined XYS and fluoxetine, respectively. The behavioral changes of the rats were observed after 21 days. The contents of pregnenolone (PREG), progesterone (PROG) and alloprognanolone (ALLO) in the plasma of rats were measured by ELISA. The levels of PREG, PROG and ALLO in the hippocampus and amygdala tissues were measured by High-performance liquid chromatography-mass spectrometry analysis(LC-MS/MS). The mRNA expressions of 3α-hydroxysteroid dehydrogenase (3α-HSD), 3β-hydroxysteroid dehydrogenase (3 β-HSD), cholesterol side-chain cleavage enzyme (P450scc) and 5α-reductase (5a-R) in the hippocampus and amygdala were detected by RT-qPCR methods. Results: There were changes in the model rats. The contents of PREG, PROG and ALLO changed similarly, which reflected in the decrease of PROG and ALLO, and the increase of PREG. The mRNA expression of P450scc was increased, and the mRNA expressions of 3α -HSD, 3 β-HSD and 5a-R were decreased. Refined XYS could improve the behaviors of rats and the biological indicators. Conclusions: There is a neurosteroid dysfunction in the brain region of depression rat model animals, and the mechanism of refined XYS depression treatment may be related to the regulation of the control of mRNA expression of related synthesis and metabolic enzymes in the hippocampus and amygdala, further affecting the contents of neurosteroids.


Author(s) Details:

Xiaoling Guo,
School of Basic Medical Science, Beijing University of Chinese Medicine, Beijing-100029, China and Beijing Fengtai District Fangzhuang Community Health Service Center, Beijing-100078, China.

Wenqi Qiu,
School of Basic Medical Science, Beijing University of Chinese Medicine, Beijing-100029, China.

Yueyun Liu,
School of Basic Medical Science, Beijing University of Chinese Medicine, Beijing-100029, China.

Yifang Zhang,
School of Basic Medical Science, Beijing University of Chinese Medicine, Beijing-100029, China.

Hongbo Zhao,
School of Basic Medical Science, Beijing University of Chinese Medicine, Beijing-100029, China.

Jiaxu Chen,
Formula-pattern Research Center, School of Traditional Chinese Medicine, Jinan University, Guangzhou-510632, Guangdong, China and School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, No. 11 North Third Ring Road Chaoyang District, Beijing-100029, China.

Please see the link here: https://stm.bookpi.org/IPTDFTPX/article/view/11272