Thiols-rich peptide from water buffalo horn keratin alleviates oxidative stress and inflammation through co-regulating Nrf2/Hmox-1 and NF-κB signaling pathway.
Wenxing WuJiayao TangWanglin BaoQiyuan FengJie ZhengMin HongSheng GuoYue ZhuSiying HuangMing ZhaoJin-Ao DuanRui LiuPublished in: Free radical biology & medicine (2024)
Water buffalo horn (WBH), a traditional Chinese medicine, is known for its antipyretic, anti-inflammatory and antioxidant properties. This study aims to investigate the therapeutic potential of WBH keratin (WBHK) and its derived thiol-rich peptide fractions (SHPF) for oxidative stress and inflammation. WBHK and SHPF were prepared and tested using various models including LPS-induced fever in rabbits, H 2 O 2 -induced oxidative damage in bEnd.3 cells, TNF-α-induced inflammation in bEnd.3 cells and LPS-induced inflammation in RAW 264.7 cells. Expression of key markers, such as Nrf2, Hmox-1 and NF-κB, were analyzed using qRT-PCR, ELISA and Western blotting. Label-free quantitative proteomic analysis was used to identify key differential proteins associated with the efficacy of SHPF. Our results demonstrated that treatment with WBHK significantly reduced body temperature after 0.5 h of administration in the fever rabbit model. SHPF could alleviate cellular inflammatory injury and oxidative damage by activating the key transcription factor Nrf2 and increasing the expression level of Hmox-1. SHPF could inhibit the NF-κB pathway by reducing IκB phosphorylation. It was also found that SHPF could reduce pro-inflammatory cytokine (IL-6, COX-2 and PGE 2 ) and inhibit the expression of VCAM-1, ICAM-1, IL-6 and MCP-1. Proteomics analysis showed that SHPF could inhibit HMGB1 expression and release. The results indicated that SHPF could significantly reduce inflammation and oxidative stress by regulating the Nrf2/Hmox-1 and NF-κB pathways. These findings suggest the potential therapeutic applications of WBH components in the treatment of oxidative stress and inflammation-related diseases.
Keyphrases
- oxidative stress
- induced apoptosis
- lps induced
- diabetic rats
- signaling pathway
- poor prognosis
- inflammatory response
- dna damage
- ischemia reperfusion injury
- pi k akt
- cell cycle arrest
- label free
- transcription factor
- binding protein
- rheumatoid arthritis
- anti inflammatory
- high glucose
- endoplasmic reticulum stress
- heat shock
- endothelial cells
- mass spectrometry
- epithelial mesenchymal transition
- nuclear factor
- drug induced
- replacement therapy
- smoking cessation