Endocrine active compounds with structural similarities to natural hormones such as 17β-estradiol (E2) and androgen are suspected to affect the human endocrine system by inducing hormone-dependent effects. This study aimed to detect the (anti-)estrogenic and (anti-)androgenic activities of mono-(2-ethylhexyl) phthalate (MEHP) by yeast estrogen/androgen bioassay (YES/YAS). In addition, the mechanism and uptake of MEHP to receptors during agonistic and antagonistic activities were investigated through the activation signal recovery test and chromatographic analysis using liquid chromatography and tandem mass spectrometry (LC-MS/MS). Estrogenic and androgenic activities of MEHP were not observed. However, MEHP exhibited anti-estrogenic (IC₅₀ = 125 μM) and anti-androgenic effects (IC₅₀ = 736 μM). It was confirmed that these inhibitory effects of MEHP were caused by receptor-mediated activity of the estrogen receptor and non-receptor-mediated activity of the androgen receptor in an activation signal recovery test. When IC₅₀ concentrations of anti-estrogenic and androgenic activity of MEHP were exposed to yeast cells, the uptake concentration observed was 0.0562 ± 0.0252 μM and 0.143 ± 0.0486 μM by LC-MS/MS analysis.

Nanomaterials are widely believed to induce toxic effects on organisms by evoking oxidative stress. We evaluated the toxic effects of nanomaterials on the cardiac and behavioral changes in Daphnia magna under varying exposure conditions. Titanium dioxide nanoparticles (TiO₂ NPs), silver nanoparticles (AgNPs), and silver nitrate (AgNO₃) were selected for the acute toxicity tests. The adverse effects of the substances on the neonates including heart rate, swimming speed, and oxidative stress were measured. The heart rate level decreased as the concentration of both NPs and silver ions (Ag⁺) increased. The average swimming speed was measured to be approximately 15 mm/min for the control group. The swimming speed generally increased with a longer exposure to both NPs although it reached a plateau at the lowest concentration of AgNPs. A similar but less clear trend was observed for Ag⁺. For all substances, the overall swimming speed exhibited no correlation or weak negative correlations with the exposure concentration. The oxidative stress levels increased after exposure compared with the control group. We conclude that aquatic nanotoxicity tests should consider multilevel physicochemical, physiological, and behavioral parameters for the official guidelines to quantify more robust adverse outcomes.

Extensive research on medicinal herbs for bioactive compounds proposes that they could replace synthetic drugs, reducing side effects and economic burdens. Especially, interest in the synergistic benefits of natural products is increasing, implying that their combined use may enhance therapeutic effectiveness. This study aimed to explore the synergetic effects of turmeric (Curcuma longa L.) and black pepper (Piper nigrum L.) extract on lung normal (MRC-5) and cancer (A549 and NCI-H292) cell lines. The turmeric extract (TM) only affected the lung cancer cell lines, but it had no impact on the MRC-5 cell line. On the other hand, the black pepper extract (BP) did not cause any damage to either the lung normal or cancer cell lines, even at concentrations of up to 400 µg/mL. Response surface methodology was used to predict the ideal synergistic concentrations (EC₅₀) of TM and BP, which were found to be 48.5 and 241.7 µg/mL, respectively. Notably, the selected condition resulted in higher cytotoxicity compared to the exposure to TM alone, indicating a potent synergetic effect. The rate of curcumin degradation under this combined treatment was significantly decreased to 49.72 ± 5.00 nmol/h/µg for A549 cells and 47.53 ± 4.78 nmol/h/µg for NCI-H292 cells, respectively, as compared to curcumin alone. Taken together, this study confirmed the potent synergistic effect of TM and BP on lung cancer cell lines. Further research is required to identify their specific synergetic mechanisms. Our findings provide crucial foundational data on the synergistic effects of TM and BP.

Secondary metabolites derived from plants, such as flavonoids, alkaloids, and terpenoids, are being increasingly utilized because of their bioactivity and ubiquitous distribution. Although their pharmacological uses and agricultural applications are well studied, their potential role as endocrine-disrupting compounds (EDCs) in non-target environmental organisms is largely unknown. This review aims to update our knowledge on the endocrine-disrupting effects induced by plant-derived metabolites in environmental testing models. We review guidelines and conceptual models for standardized testing approaches used to assess endocrine disruption and identify critical data gaps in the context of mammalian test systems compared to those for environmental species. We also emphasize the known endocrine mechanisms, including the regulation of estrogen and thyroid pathways and their effects on reproduction and hormonal regulation in environmental species. By integrating evidence across diverse biological systems, this work intends to provide a link between toxicological and ecological perspectives on the emerging role of plant-derived metabolites as potential EDCs in natural ecosystems. Importantly, we highlight that an extensive assessment of plant-derived metabolites is required to improve understanding of their ecological hazards and the mechanisms of their effects.

Numerous studies derived from medicinal herbs have been conducted to explore bioactive compounds as potential alternatives to synthetic drugs, aiming to mitigate harmful side effects and alleviate economic burdens. In this study, we assessed the safety and potential biological activities of extracts from Fomes fomentarius L. (FFL). The FFL extracts were obtained through various ethanol concentrations, as follows: 0%, 30%, 50%, 70%, and 100%, respectively. All extracts did not induce mutagenicity even up to 5 mg/plate concentration. In the assessment of antioxidant activity, only the hot water extract exhibited weaker antioxidant activity than the other ethanol extracts. Notably, all extracts exhibited significant antimutagenetic effects only with a metabolically active enzyme system (S9 mix). The condition of 70% ethanol extract displayed the most robust antimutagenic activity; thus, the extract was sequentially fractionated with solvents of varying polarities to isolate inhibitory components. After the fractionization, the diethyl ether and butanol fractions effectively suppressed the growth of mutated colonies, suggesting that those such as essential oils, vitamins, alkaloids, and flavonoids can be considered major active compounds. Overall, our study demonstrated that FFL extracts induce potent antioxidant and antimutagenic effects. Further investigations are warranted to verify specific active compounds which induce an antimutagenic effect. Our findings provide valuable insights into FFL as a promising source for potential functional food development.