Beeswax by-Products Efficiently Counteract the Oxidative Damage Induced by an Oxidant Agent in Human Dermal Fibroblasts.
Francesca GiampieriMassimiliano GasparriniTamara Yuliett Forbes-HernándezPiera Pia MannaJiaojiao ZhangPatricia Reboredo-RodríguezDanila CianciosiJosé Luis QuilesCristina Torres Fernández-PiñarFrancisco Josè Orantes-BermejoStefano BompadreSadia AfrinMaurizio Antonio BattinoPublished in: International journal of molecular sciences (2018)
The antioxidant capacity and the phytochemical composition of two by-products from beeswax recycling processes were recently investigated. The aim of the present work was to evaluate the efficacy of one of these by-products, MUD1, against the oxidative stress induced by 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) in human dermal fibroblast (HDF) cells. After a preliminary viability assay, the protective effect of MUD1 was investigated through the measurement of apoptosis level, the reactive oxygen species (ROS) and nitrite (NO₂-) production, the level of protein and lipid biomarkers (carbonyl groups, total glutathione and thiobarbituric acid-reactive substance) of oxidative damage, and the measurement of antioxidant enzymes activities (glutatione peroxidase, glutathione reductase, glutathione transferase, superoxide dismutase and catalase). The obtained results showed that MUD1 exerted protective effects on HDF, increasing cell viability and counteracted the oxidative stress promoted by AAPH-treatment, and improved mitochondria functionality and wound healing capacities. This work shows the antioxidant effects exerted by beeswax by-products, demonstrating for the first time their potential against oxidative stress in human dermal fibroblast cells; however, further research will be necessary to evaluate their potentiality for human health by more deeply in vitro and in vivo studies.
Keyphrases
- oxidative stress
- induced apoptosis
- wound healing
- endothelial cells
- reactive oxygen species
- human health
- cell cycle arrest
- cell death
- dna damage
- endoplasmic reticulum stress
- ischemia reperfusion injury
- risk assessment
- induced pluripotent stem cells
- diabetic rats
- pluripotent stem cells
- anti inflammatory
- signaling pathway
- nitric oxide
- hydrogen peroxide
- small molecule
- combination therapy
- smoking cessation