Among the world’s leading causes of cardiovascular disease, atherosclerosis is a chronic inflammatory disorder that affects the arteries. Both vasodilation and vasoconstriction, low levels of nitric oxide and high levels of reactive oxygen species and pro-inflammatory factors characterize dysfunctional blood vessels. Hypertension, and atherosclerosis, all start with this dysfunction. Geraniol, a compound of acyclic monoterpene alcohol, found in plants such as geranium, lemongrass and rose, is a primary constituent of essential oils. It shows a variety of pharmacological properties. This study aimed to investigate the impact of geraniol on Ox-LDL-induced stress and inflammation in human umbilical vein endothelial cells. In this study, HUVECs were treated with Ox-LDL or geraniol at different dose concentrations. MTT assay, Western blot, ROS generation and DNA fragmentation were used to evaluate geraniol’s effects on Ox-LDL-induced HUVECs inflammation. The results show that geraniol pre-incubation ameliorates Ox-LDL-mediated HUVECs cytotoxicity and DNA fragmentation. The geraniol inhibited the production of pro-inflammatory cytokines by Ox-LDL, including TNF-α, IL-6 and IL-1β. In Ox-LDL-stimulated HUVECs, geraniol suppresses the nuclear translocation and activity of NF-ᴋB as well as phosphorylation of IkBα. Moreover, geraniol activated the PI3K/AKT/NRF2 pathway in HUVECs, resulting in an increase in the expression of HO-1. Taking our data together, we can conclude that, in HUVECs, geraniol inhibits Ox-LDL-induced inflammation and oxidative stress by targeting PI3/AKT/NRF2.

Hepatotoxic contaminants such as zearalenone (ZEA) are widely present in foods. Marine algae have a wide range of potential applications in pharmaceuticals, cosmetics, and food products. Research is ongoing to develop treatments and products based on the compounds found in algae. Fucoxanthin (FXN) is a brown-algae-derived dietary compound that is reported to prevent hepatotoxicity caused by ZEA. This compound has multiple biological functions, including anti-diabetic, anti-obesity, anti-microbial, and anti-cancer properties. Furthermore, FXN is a powerful antioxidant. In this study, we examined the effects of FXN on ZEA-induced stress and inflammation in HepG2 cells. MTT assays, ROS generation assays, Western blots, and apoptosis analysis were used to evaluate the effects of FXN on ZEA-induced HepG2 cell inflammation. Pre-incubation with FXN reduced the cytotoxicity of ZEA toward HepG2 cells. FXN inhibited the ZEA-induced production of pro-inflammatory cytokines, including IL-1 β, IL-6, and TNF-α. Moreover, FXN increased HO-1 expression in HepG2 by activating the PI3K/AKT/NRF2 signaling pathway. In conclusion, FXN inhibits ZEA-induced inflammation and oxidative stress in hepatocytes by targeting Nrf2 via activating PI3K/AKT signaling.

Silybum marianum is a medicinal plant that produces silybins A and B, which exhibit liver-protective activities. The He–Ne laser pre-sowing seed treatment has been used as a physical biostimulator in numerous plants to promote seed germination, plant growth, and secondary metabolite production. Thus, in this study, a He–Ne laser at 632.8 nm was used to irradiate S. marianum seeds with the aim of promoting plant growth as well as enhancing the production of silybin (A + B). The seeds were irradiated with a He–Ne laser for 2, 4, 6, 8, and 10 min. The growth attributes of the plants, as well as the silybin (A + B) content and bioactivities of fruit extracts from various treatment groups, were compared. The results indicated that all laser seed treatments resulted in a subsequent increase in plant growth, with the highest yield observed in the 10 min laser treatment. An increase in fruit silybin (A + B) content and in chalcone synthase gene expressions were observed in plants from the 6-, 8-, and 10-min laser-irradiated seeds. The highest silybin (A + B) contents were observed in plants from the 6-min-irradiated seeds. Furthermore, the corresponding fruit extract also exhibited elevated cell growth inhibition in the Dictyostelium discoideum cell model.

Moringa oleifera Lam (MO) is a member of the Moringaceae family and has been widely used as a traditional form of treatment for various diseases due to its high nutrient content. The plant is rich in vitamins, minerals, organic acids, phenolic compounds, polyphenols, alkaloids, and flavonoids. However, the concentrations of these components in each part of the plant differ, leading to specific beneficial uses. In this study, we aimed to analyze the contents of Moringa oleifera leaf (ML) and Moringa oleifera root (MR) extracts and characterize the effects of these extracts on cell behavior. HPLC analysis data showed a higher level of flavonoids and apigenin in the ML extract compared to the MR extract. Furthermore, CG/MS analysis revealed 54 components in the ML extract, with only 3 (ethyl palmitate, ethyl linolenate, and palmitic acid, 2-(octadecyloxy)ethyl ester) of them being at high levels. In this study, Dictyostelium discoideum was used as a cellular model and D. discoideum’s cell growth, chemotaxis, and development life cycle were investigated. The data presented herein demonstrate a significant decrease in cell growth and that the completion of the development life cycle was delayed in the ML extract-treated sample. This effect was not found in the untreated cells and MR extract-treated samples. In addition, the ability of cells to stream during chemotaxis was not inhibited following treatments. These findings suggested that ML extract has an impact on cell proliferation and cell directed migration processes, where the high level of flavonoids and apigenin in this extract can be a strong factor that led to these results.