Bioconversion of Ginsenosides in American Ginseng Extraction Residue by Fermentation with Ganoderma lucidum Improves Insulin-like Glucose Uptake in 3T3-L1 Adipocytes

Ginseng is one of the most popular traditional Chinese medicines that have been widely used in China and other Asian countries for thousands of years. Ginsenosides are the unique bioactive saponins occurring in ginseng, and their biological activities have been extensively investigated. A large amount of ginseng residue is produced as waste product due to its applications in manufacturing functional food products, even though it may still contain bioactive components. Thus, the objective of this study was to investigate the hypoglycemic activities of American ginseng extraction residue (AmR) via fermentation with Ganoderma lucidum. Our results showed that the total phenolic contents and β-glucosidase activity of AmR profoundly increased after fermentation with G. lucidum. In 3T3-L1 adipocytes, stimulation of glucose uptake by treatment with AmR was not significant, while fermented AmR (FAmR) exhibited insulin-like glucose-uptake-stimulatory effects. Importantly, the hypoglycemic effects of FAmR were positively associated with the amount of the deglycosylated minor ginsenosides Rg1, Rg3, and compound K. Taken together, our current findings suggest that bioconversion of AmR by fermentation with G. lucidum may be a feasible and eco-friendly approach to developing a functional ingredient for the management of diabetes, while also resolving the problem of ginseng waste.

Ginsenoside Compound K Assisted G-Quadruplex Folding and Regulated G-Quadruplex-Containing Transcription

Ginsenoside compound K (CK) is one of the major metabolites of the bioactive ingredients in Panax ginseng, which presents excellent bioactivity and regulates the expression of important proteins. In this work, the effects of CK on G-quadruplexes (G4s) were quantitatively analyzed in the presence and absence of their complementary sequences. CK was demonstrated to facilitate the formation of G4s, and increase the quantity of G4s in the competition with duplex. Thermodynamic experiments suggested that the electrostatic interactions were important for G4 stabilization by CK. CK was further found to regulate the transcription of G4-containing templates, reduce full-length transcripts, and decrease the transcription efficiency. Our results provide new evidence for the pharmacological study of ginsenosides at the gene level.

Ocean Waves in K-distributed Clutter

<div> <div> <div> <p>Two examples of low grazing angle radar sea clutter, both well described by the compound K-distribution model, are studied. Pulse Doppler processing is applied to obtain two dimensional range-time textures for the intensity, centroid and width of the Doppler spectrum. The first example exhibits a monochromatic swell pattern, allowing phase averaging to be applied to the textures. The second example has a more typical ocean wave spectrum. The intensity textures are gamma distributed, consistent with the compound K-distribution model, but the Doppler spectrum centroid and width textures are also found to be gamma distributed. Based on this analysis, a new method for simulation of coherent radar sea clutter is proposed, where separate memoryless nonlinear transformations are applied to a simulated water surface to generate the spatially and temporally varying intensity, centroid and width of the Doppler spectrum. The method builds on the evolving Doppler spectrum model for radar sea clutter simulation and established methods for simulation of water surfaces. </p> </div> </div> </div>

Ocean Waves in K-distributed Clutter

<div> <div> <div> <p>Two examples of low grazing angle radar sea clutter, both well described by the compound K-distribution model, are studied. Pulse Doppler processing is applied to obtain two dimensional range-time textures for the intensity, centroid and width of the Doppler spectrum. The first example exhibits a monochromatic swell pattern, allowing phase averaging to be applied to the textures. The second example has a more typical ocean wave spectrum. The intensity textures are gamma distributed, consistent with the compound K-distribution model, but the Doppler spectrum centroid and width textures are also found to be gamma distributed. Based on this analysis, a new method for simulation of coherent radar sea clutter is proposed, where separate memoryless nonlinear transformations are applied to a simulated water surface to generate the spatially and temporally varying intensity, centroid and width of the Doppler spectrum. The method builds on the evolving Doppler spectrum model for radar sea clutter simulation and established methods for simulation of water surfaces. </p> </div> </div> </div>

Biochemical Targets and Molecular Mechanism of Ginsenoside Compound K for Treating Osteoporosis Based on Network Pharmacology

Ginsenosides have been proven to be potential beneficial in treatment of osteoporosis. To investigate the potential of ginsenosides in osteoporosis, ginsenoside compound K (GCK) was selected to explore the potential therapy targets and mechanism based on network pharmacology (NP). 206 and 6590 targets were obtained for GCK and osteoporosis, respectively, in which 138 targets were identified as co-targets of GCK and osteoporosis based on intersection analysis. Five central gene clusters and hub genes (STAT3, PIK3R1, VEGFA, JAK2 and MAP2K1) were identified through protein-protein interaction network analysis. Gene Ontology (GO) enrichment implied that phosphatidylinositol-related biological process, molecular modification and function may play an important role for GCK in treatment and prevention of osteoporosis. Functions and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis suggested that 16 targets were enriched in the osteoclast differentiation. Also, except for being identified as hub targets, MAPK and phosphatidylinositol-related proteins were enriched in the downstream signaling of c-Fms in the osteoclast differentiation pathway. Molecular docking further confirmed that GCK could interact with active cavity on the surface of c-Fms (osteoclast differentiation-related membrane receptor), and their complex could be stabilized by three H-bonds with residues including Glu 664 (3.19 Å), Glu 664 (2.62 Å) and Cys 666 (2.78 Å). Summarily, GCK could interfere the occurrence and progress of osteoporosis through c-Fms-mediated MAPK and phosphatidylinositol-related signaling regulating osteoclast differentiation.

Synthesis, crystal structure and selected properties of K2[Ni(dien)2]{[Ni(dien)]2Ta6O19}·11 H2O

The new compound K2[Ni(dien)2]{[Ni(dien)]2Ta6O19}·11 H2O crystallized at room temperature applying a diffusion based reaction in a H2O/DMSO mixture using K8{Ta6O19}·16 H2O, Ni(NO3)2·6H2O and dien (diethylenetriamine). In the crystal structure, the Lindqvist-type anion [Ta6O19]8– is structurally expanded by two octahedrally Ni2+-centered complexes via three Ni–µ 2-O–Ta bonds thus generating the new {[Ni(dien)]2Ta6O19}4– anion. Two KO8 polyhedra share a common edge to form a K2O14 moiety, which connects the {[Ni(dien)]2Ta6O19}4– cluster shells into chains. The isolated [Ni(dien)2]2+ complexes are located in voids generated by the structural arrangement of the chains. An extended hydrogen bonding network between the different constituents generates a 3D network. The crystal water molecules can be thermally removed to form a highly crystalline dehydrated compound. Partial water uptake leads to the formation of a crystalline intermediate with a reduced unit cell volume compared to the fully hydrated sample. Water sorption experiments demonstrate that the fully dehydrated sample can be fully reconverted to the hydrated compound. The crystal field splitting parameters for the octahedrally coordinated Ni2+-centered complexes have been evaluated from an UV/Vis spectrum yielding D q = 1056 cm−1 and B = 887 cm−1.