Antioxidant and Anti-Inflammatory Properties of Hydrolyzed Royal Jelly Peptide in Human Dermal Fibroblasts: Implications for Skin Health and Care Applications.
Chang-Yu YanQian-Qian ZhuCheng-Xi GuanGui-Lan XiongXin-Xing ChenHai-Biao GongJia-Wei LiShu-Hua OuyangHiroshi KuriharaYi-Fang LiRong-Rong HePublished in: Bioengineering (Basel, Switzerland) (2024)
Hydrolyzed royal jelly peptide (RJP) has garnered attention for its health-promoting functions. However, the potential applications of RJP in skincare have not been fully explored. In this study, we prepared RJP through the enzymatic hydrolysis of royal jelly protein with trypsin and investigated its antioxidant and anti-inflammatory properties on primary human dermal fibroblasts (HDFs). Our results demonstrate that RJP effectively inhibits oxidative damage induced by H 2 O 2 and lipid peroxidation triggered by AAPH and t -BuOOH in HDFs. This effect may be attributed to the ability of RJP to enhance the level of glutathione and the activities of catalase and glutathione peroxidase 4, as well as its excellent iron chelating capacity. Furthermore, RJP modulates the NLRP3 inflammasome-mediated inflammatory response in HDFs, suppressing the mRNA expressions of NLRP3 and IL-1β in the primer stage induced by LPS and the release of mature IL-1β induced by ATP, monosodium urate, or nigericin in the activation stage. RJP also represses the expressions of COX2 and iNOS induced by LPS. Finally, we reveal that RJP exhibits superior antioxidant and anti-inflammatory properties over unhydrolyzed royal jelly protein. These findings suggest that RJP exerts protective effects on skin cells through antioxidative and anti-inflammatory mechanisms, indicating its promise for potential therapeutic avenues for managing oxidative stress and inflammation-related skin disorders.
Keyphrases
- anti inflammatory
- nlrp inflammasome
- oxidative stress
- umbilical cord
- healthcare
- inflammatory response
- wound healing
- endothelial cells
- induced apoptosis
- public health
- soft tissue
- mesenchymal stem cells
- hydrogen peroxide
- induced pluripotent stem cells
- mental health
- binding protein
- pluripotent stem cells
- palliative care
- signaling pathway
- extracellular matrix
- protein protein
- human health
- working memory
- machine learning
- lipopolysaccharide induced
- climate change
- nitric oxide
- single cell
- risk assessment
- genome wide
- dna methylation
- nitric oxide synthase
- fatty acid
- pain management
- diabetic rats
- ischemia reperfusion injury
- single molecule