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Flavonoids from Polygonum hydropiper L. regulate PCV2-induced oxidative stress of RAW264.7 cells via Pi3k/AKT and
Qi Chen1, Qiuhua Wang1, Yi Zhao1
1College of Animal Science and Technology, Guangxi University, Nanning, 530005, People's Republic of China.
Abstract:
Flavonoid n-butanol (FNB) possess diverse pharmacological properties. This study aimed to explore the mechanism of FNB in regulating oxidative response in PCV2-infected RAW264.7 cells. PCV2-infected macrophages were treated with FNB, and oxidative stress markers, antioxidant enzyme activities, as well as related gene and protein expression were assessed to evaluate FNB's regulatory effects. Specifically, the level of Nitric Oxide (NO), Total antioxidant capacity (T-AOC), anti-hydroxyl radical capacity, anti-superoxide anion capacity, L-Glutathione (GSH) level, Super Oxide Dismutase (SOD) and Catalase (CAT) were detected. The expression of key oxidative stress-related and signaling pathway genes and proteins was determined by qPCR and western blotting, respectively. The results indicated that FNB reduced intracellular ROS, increased SOD and CAT activities, improved antioxidant capacity, upregulated the mRNA expression levels of HO-1, NQO1, Nrf2, Pi3kca, SOD, and HDAC1, downregulated AKT, Keap1, and HAT1, enhanced HDAC1 activity, and inhibited HAT activity. In conclusion, FNB protects against PCV2-induced oxidative damage by activating the PI3K/AKT pathway and inhibiting Keap1, which collectively enhance the Nrf2/HO-1 antioxidant response.
Insights
Flavonoid n-butanol (FNB) protects against oxidative damage caused by PCV2 infection. It enhances the Nrf2/HO-1 antioxidant response by activating the PI3K/AKT pathway and inhibiting Keap1.
Area of Science:
- Pharmacology
- Cell Biology
- Immunology
Background:
- Porcine circovirus type 2 (PCV2) infection causes oxidative stress in macrophages.
- Flavonoid n-butanol (FNB) exhibits various pharmacological activities.
- Understanding FNB's mechanism against PCV2-induced oxidative damage is crucial.
Purpose of the Study:
- To investigate the protective mechanism of FNB against PCV2-induced oxidative stress in RAW264.7 cells.
- To elucidate FNB's role in regulating antioxidant enzymes and related signaling pathways.
Main Methods:
- PCV2-infected RAW264.7 cells were treated with FNB.
- Assessed oxidative stress markers (ROS, NO, T-AOC, GSH).
- Measured antioxidant enzyme activities (SOD, CAT) and gene/protein expression (qPCR, Western blotting).
Main Results:
- FNB reduced intracellular ROS and improved antioxidant capacity.
- FNB increased SOD and CAT activities.
- FNB modulated key genes/proteins in the PI3K/AKT/Nrf2/HO-1 pathway, including upregulation of Nrf2 and HO-1, and downregulation of Keap1.
Conclusions:
- FNB exerts protective effects against PCV2-induced oxidative damage.
- FNB activates the PI3K/AKT pathway and inhibits Keap1.
- This action collectively enhances the Nrf2/HO-1 antioxidant response, mitigating oxidative stress.
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