Search Results (3)

Gerbera piloselloides (L.)Cass. is an important ethnomedicinal plant. Wild populations are steadily declining, however, posing a risk of failure to meet future market demand. Investigating suitable habitats for this plant and key influencing factors is crucial for its artificial cultivation. In this study, we implemented an optimized MaxEnt to project suitable habitats for the target species in five different periods and explored the impact of different environmental variables on its distribution. Our study findings provide confirmation of the following: (1) The current and future potential distributions of Gerbera piloselloides are primarily located in the areas south of the Qinling–Huaihe boundary in China, with future expansions expected to shift northward and westward. (2) Notably, there was a contraction in the junction regions of the provinces of Jiangxi, Anhui, Hunan, and Hubei. (3) The number of highly suitable habitats in Fujian, Guangdong, Yunnan, and Guangxi is expanding; in comparison, the number in Guizhou, Sichuan, and Hainan is declining. (4) The primary environmental determinants shaping its range, together with the threshold values for highly suitable habitats, are the minimum temperature of the coldest month (bio6, 0.88–22.58 °C) and the temperature seasonality (bio4, 461.54–763.9). The findings presented in this work provide support for the artificial cultivation and conservation of this plant. Full article

Gerbera piloselloides, a plant in the Asteraceae family, is a traditional Chinese medicinal herb known for its unique therapeutic properties, including reported anti-tumor and antioxidant effects. Recent studies suggest that the main constitute of G. piloselloides, coumarins, may have potential anti-tumor activity. Recent research suggests that coumarins, the active compounds in G. piloselloides, may hold potential anti-tumor activity. However, the pharmacodynamic constituents remain unidentified. This study aims to isolate and characterize the bioactive compounds of G. piloselloides and to assess its anti-tumor effects. Initially, seven compounds, including coumarins, a ketone, and a furanolide, were isolated and identified from G. piloselloides by semi-preparative high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) analysis. The anti-tumor effects of these compounds were evaluated across four different cancer cell lines. Among them, the compound cyclobrachycoumarin showed a significant inhibitory effect on colorectal cancer (CRC) cell proliferation and was selected for further investigation. Cyclobrachycoumarin was found to induce CRC cell apoptosis and cell cycle arrest in a dose-dependent manner. This treatment also led to increased levels of ROS and cleaved PARP, along with decreased expressions of survivin, cyclin D1, and CDK1. In vivo studies further demonstrated that cyclobrachycoumarin effectively reduced tumor growth in HT-29 xenograft models by promoting apoptosis and cell cycle arrest, with a favorable tolerability profile. In summary, this study suggests that cyclobrachycoumarin may be a promising candidate for safe and effective CRC therapy. Full article

Crude ethyl acetate extract of Gerbera piloselloides (L.) Cass. was investigated by dual high-resolution PTP1B/α-glucosidase inhibition profiling and LC-PDA-HRMS. This indicated the presence of a series of unprecedented prenyl- and geranyl-substituted coumarin derivatives correlated with both α-glucosidase and PTP1B inhibitory activity. Repeated chromatographic separation targeting these compounds led to the isolation of 13 new compounds, of which ten could be isolated as both enantiomers after chiral separation. The structures of all isolated compounds were characterized by HRMS and extensive 1D and 2D NMR analysis. The absolute configurations of the isolated compounds were determined by comparison of experimental and calculated electronic circular dichroism spectra. Compound 6 features a rare furan-oxepane 5/7 ring system, possibly formed through addition of a geranyl unit to C-3 of 5-methylcoumarin, representing a new type of geranyl-substituted coumarin skeleton. Compounds 19 and 24 are the first examples of dimeric natural products consisting of both coumarin and chromone moieties. Full article