Maqui Berry and Ginseng Extracts Reduce Cigarette Smoke-Induced Cell Injury in a 3D Bone Co-Culture Model.
Shun-Cong ZhangWeidong WengShuncong ZhangHelen RinderknechtBianca BraunRegina BreinbauerPurva GuptaAshok KumarSabrina EhnertTina HistingAndreas K NusslerRomina H Aspera-WerzPublished in: Antioxidants (Basel, Switzerland) (2022)
Cigarette smoking-induced oxidative stress has harmful effects on bone metabolism. Maqui berry extract (MBE) and ginseng extract (GE) are two naturally occurring antioxidants that have been shown to reduce oxidative stress. By using an osteoblast and osteoclast three-dimensional co-culture system, we investigated the effects of MBE and GE on bone cells exposed to cigarette smoke extract (CSE). The cell viability and function of the co-culture system were measured on day 14. Markers of bone cell differentiation and oxidative stress were evaluated at gene and protein levels on day 7. The results showed that exposure to CSE induced osteoporotic-like alterations in the co-culture system, while 1.5 µg/mL MBE and 50 µg/mL GE improved CSE-impaired osteoblast function and decreased CSE-induced osteoclast function. The molecular mechanism of MBE and GE in preventing CSE-induced bone cell damage is linked with the inhibition of the NF-κB signaling pathway and the activation of the Nrf2 signaling pathway. Therefore, MBE and GE can reduce CSE-induced detrimental effects on bone cells and, thus, prevent smoking-induced alterations in bone cell homeostasis. These two antioxidants are thus suitable supplements to support bone regeneration in smokers.
Keyphrases
- oxidative stress
- diabetic rats
- bone regeneration
- bone mineral density
- induced apoptosis
- signaling pathway
- high glucose
- single cell
- drug induced
- epithelial mesenchymal transition
- stem cells
- mesenchymal stem cells
- pi k akt
- endothelial cells
- postmenopausal women
- cell death
- small molecule
- body composition
- cell therapy
- immune response
- endoplasmic reticulum stress
- cell cycle arrest
- ischemia reperfusion injury
- bone marrow
- toll like receptor
- mass spectrometry
- inflammatory response
- protein protein
- hydrogen peroxide