ABSTRACT
Camellia polyodonta flowers contain limited information available regarding the composition of their bioactive compounds and activity. The objective of this study was to identify phenolic compounds and investigate the effect of different solvents (ethanol and methanol) on the phenolic content and antioxidant activity in C. polyodonta flowers. The analysis using UPLC-Q-TOF-MS/MS revealed the presence of 105 phytochemicals and the most common compounds were flavonols, procyanidins, and ellagitannins. Interestingly, flavonol triglycosides were identified for the first time in these flowers. The study demonstrated that the concentration of the solvent had a significant impact on the total phenolic compound (TPC), total flavonoid compound (TFC), and total proanthocyanidin content (TPAC). The TPC, TFC, and TPAC showed a remarkable increase with the increasing concentration of the solvent, reaching their maximum levels (138.23 mg GAE/g DW, 421.62 mg RE/g DW, 60.77 mg PB2E/g DW) at 70% ethanol. However, the total anthocyanin content reached its maximum at low concentrations (0.49 mg CGE/g DW). Similar trends were observed in the antioxidant activity, as measured by the DPPH· assay (DPPH radical scavenging activity), ABTS·+ assay (ABTS radical cation scavenging activity), and FRAP assay (Ferric reducing antioxidant power). The maximum antioxidant activity was observed at 100% solvents and 70% methanol. Among the 14 individual phenolic compounds, 70% methanol yielded the highest content for 8 (cyanidin-3-O-glucoside, procyanidin B2, procyanidin B4, epicatechin, rutin, kaempferol-3-O-rutinoside, astragaline and quercitrin) out of the 14 compounds. Additionally, it was found that epicatechin was the most abundant phenolic compound, accounting for approximately 20339.37 µg/g DW. Based on these findings, it can be concluded that 70% methanol is the most effective solvent for extracting polyphenols from C. polyodonta flowers. These results provided chemical information and potential antioxidant value for further research in C. polyodonta flowers.
ABSTRACT
Camellia polyodonta flowers are rich sources of phenolics and less attention has been paid to their potential biological activity. This study aims to explore the crude extracts and resulting purified fractions (CPFP-I, II, III, and IV) through compositional analysis and antioxidant and hypolipidemic activities in vitro and in vivo. Among four fractions, CPFP-II contained the highest total phenolic content and flavonoid content, while CPFP-III exhibited the greatest total proanthocyanidin content. Among the 14 phenolic compounds, CPFP-II displayed the highest content of procyanidin B2, B4, and C1, whereas CPFP-III contained the highest amount of 1,2,3,6-tetragalloylglucose. The DPPH, ABTS, and FRAP assessments demonstrated a consistent trend: CPFP-II > CPFP-III > CPFP-I > CPFP-IV. In vivo experiments showed that that all four fractions significantly reduced lipid levels in hyperlipidemic C. elegans (p < 0.05), with CPFP-II exhibiting the most potent effect. Furthermore, CPFP-II effectively bound to bile acids and inhibited the enzymatic activity of pancreatic lipase in vitro. Consequently, CPFP-II should be prioritized as a promising fraction for further exploration and should provide substantial support for the feasibility of the C. polyodonta flower as a natural alternative.
ABSTRACT
Litsea pungens is a plant with medicinal and edible properties, where the fruits are edible and the leaves have medicinal properties. However, there is limited research on the chemical and pharmacological activities of the plant. In this study, essential oils were extracted by steam distillation and their antioxidant and antibacterial activities were further evaluated. Gas chromatography-mass spectrometry (GC-MS) was used to identify the chemical components of L. pungens fresh fruit essential oil (FREO) and L. pungens fresh flower essential oil (FLEO), rapeseed oil (RO) and commercial Litsea oil (CEO). The results showed that 12 chemical components were identified in FREO. Twelve chemical components were identified from FLEO, four chemical components were identified from CEO, and thirteen chemical components were identified from RO. Except for RO, the other three oils were mainly composed of terpenes, among which limonene is the main chemical component. In terms of antioxidant activity, FREO, FLEO, CEO and RO have antioxidant capacity, mainly reflected in the scavenging DPPH free radicals and the iron ion chelating ability, and the antioxidant activity shows a certain dose effect, but the antioxidant activity of FLEO is the weakest among the four oils. Meanwhile, under the stress of hydrogen peroxide, CEO demonstrated a significant antioxidant protective effect on cells. It is worth mentioning that compared with the positive control, the FREO exhibited a better antibacterial rate. When the concentration of essential oil is 20 mg/mL, the bacteriostatic rate can reach 100%. Therefore, it could be a promising candidate among medicinal and edible plants.
Subject(s)
Litsea , Oils, Volatile , Antioxidants/pharmacology , Antioxidants/chemistry , Oils, Volatile/pharmacology , Oils, Volatile/chemistry , Litsea/chemistry , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Terpenes , Plant Oils/pharmacology , Plant Oils/chemistryABSTRACT
Camellia oil (CO) is a high medicinal and nutritional value edible oil. However, its ability to alleviate fat accumulation in high-fat Caenorhabditis elegans has not been well elucidated. Therefore, this study aimed to investigate the effect of CO on fat accumulation in high-fat C. elegans via transcriptome and metabolome analysis. The results showed that CO significantly reduced fat accumulation in high-fat C. elegans by 10.34% (Oil Red O method) and 11.54% (TG content method), respectively. Furthermore, CO primarily altered the transcription levels of genes involved in longevity regulating pathway. Specifically, CO decreased lipid storage in high-fat C. elegans by inhibiting fat synthesis. In addition, CO supplementation modulated the abundance of metabolic biomarkers related to pyrimidine metabolism and riboflavin metabolism. The integrated transcriptome and metabolome analyses indicated that CO supplementation could alleviate fat accumulation in high-fat C. elegans by regulating retinol metabolism, drug metabolism-cytochrome P450, metabolism of xenobiotics by cytochrome P450, ascorbate and aldarate metabolism, and pentose and glucuronate interconversions. Overall, these findings highlight the potential health benefits of CO that could potentially be used as a functional edible oil.
Subject(s)
Caenorhabditis elegans Proteins , Camellia , Animals , Caenorhabditis elegans/metabolism , Transcriptome , Camellia/genetics , Camellia/metabolism , Caenorhabditis elegans Proteins/metabolism , Lipid Metabolism , MetabolomeABSTRACT
The flowers, leaves, seed cakes and fruit shells of Camellia oleifera are rich in bioactive polysaccharides, which can be used as additives in food and other industries. In this study, a Box-Behnken design was used to optimize the extraction conditions of polysaccharides from C. oleifera flowers (P-CF), leaves (P-CL), seed cakes (P-CC), and fruit shells (P-CS). Under the optimized extraction conditions, the polysaccharide yields of the four polysaccharides were 9.32% ± 0.11 (P-CF), 7.57% ± 0.11 (P-CL), 8.69% ± 0.16 (P-CC), and 7.25% ± 0.07 (P-CS), respectively. Polysaccharides were mainly composed of mannose, rhamnose, galacturonic acid, glucose, galactose, and xylose, of which the molecular weights ranged from 3.31 kDa to 128.06 kDa. P-CC had a triple helix structure. The antioxidant activities of the four polysaccharides were determined by Fe2+ chelating and free radical scavenging abilities. The results showed that all polysaccharides had antioxidant effects. Among them, P-CF had the strongest antioxidant activity, of which the highest scavenging ability of DPPHâ¢, ABTSâ¢+, and hydroxyl radical could reach 84.19% ± 2.65, 94.8% ± 0.22, and 79.97% ± 3.04, respectively, and the best chelating ability of Fe2+ could reach 44.67% ± 1.04. Overall, polysaccharides extracted from different parts of C. oleifera showed a certain antioxidant effect, and could be developed as a new type of pure natural antioxidant for food.
ABSTRACT
Nitrogen cycling in soil, which associated with microbes, plays an important role in plant growth. Irrational application of nitrogen fertilizer could disrupt the structure of soil microbial community, thus inhibiting the uptake of nitrogen by plants and increasing nitrogen leaching in soil. Field and pot leaching experiments with the combined application of chitin fertilizer and selenium (Se) were carried out in order to develop an approach to improve the efficiency of nitrogen fertilizer utilization and reduce runoff by nitrogen loss in orchards of Guanxi pomelo in Fujian Province. Our results showed that application of chitin fertilizer combined with Se to the soil with reduced nitrogen and phosphate fertilizer (nitrogen fertilizer decreased by 25% and phosphate fertilizer decreased by 50%) could significantly increase the fruit yield, vitamin C and solid-acid ratio in the fruit. The application of chitin fertilizer and Se can not only lead to the increase of total nitrogen content in plant leaves but also the alkali-hydrolyzable nitrogen content in soil which enhancing soil nitrogen supplying capacity. It has been found that the adding the chitin fertilizer and Se into soil can significantly affect the structure and functional categories microbial communities and its activities. This is directly evidenced by the findings that the expression level of several groups of N metabolism and transporting related genes (i.e. amoAB and nxrA in nitrification, narG, nirK, norBC, and nosZ in denitrification, nirD, narH in dissimilatory nitrogen reduction, and ureC in ammoniation) has been drastically up-regulated. Our results indicate this strategy for reducing N and P input while maintaining and improving plant performance by supplementing with micronutrient Se and chitin fertilizer can increase the fruit yield and improve the quality of Guanxi pomelo through improving fertilizer use efficiency.
Subject(s)
Selenium , Soil , Chitin , Fertilizers/analysis , Fruit/chemistry , Nitrogen/analysisABSTRACT
Eucalyptus grandis × E. urophylla was a unique hybridization in China. However, the chemical and pharmacological properties were rarely reported. Therefore, in this work, we used a steam distillation method to obtain essential oils from leaves of E. grandis × E. urophylla, and further evaluated the antioxidant, antimicrobial, and phytotoxic potential of the essential oil. Gas chromatography mass spectrometry (GC-MS) was applied to investigate the chemical composition of E. grandis × E. urophylla essential oil (EEO) and the results showed that the main components of EEO were monoterpenes followed by sesquiterpenes. Among them, α-pinene accounted about 17.02%. EEO could also well scavenge 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2, 2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) free radicals showing a good free radical clearance ability. In addition, EEO efficiently inhibited the growth of six kinds of bacteria as well as seven kinds of plant pathogens, especially Salmonella typhimurium and Colletotrichum gloeosporioides. Moreover, the seedling germination of Raphanus sativus, Lactuca sativa, Lolium perenne, and Bidens pilosa was significantly suppressed by EEO, thus, indicating essential oils from eucalyptus possessed an excellent phytotoxic activity. This study may give a better understanding on EEO and provide a pharmacological activities analysis contributing to the further research of EEO as a functional drug in agronomic and cosmetic industries.
Subject(s)
Anti-Bacterial Agents/pharmacology , Antifungal Agents/pharmacology , Antioxidants/pharmacology , Eucalyptus Oil/chemistry , Eucalyptus Oil/pharmacology , Anti-Bacterial Agents/chemistry , Antifungal Agents/chemistry , Antioxidants/chemistry , Eucalyptus/chemistry , Eucalyptus Oil/analysis , Eucalyptus Oil/toxicity , Gas Chromatography-Mass Spectrometry , Germination/drug effects , Lactuca/drug effects , Microbial Sensitivity Tests , Plant Leaves/chemistry , Seeds/drug effectsABSTRACT
Polycyclic aromatic hydrocarbons (PAHs) are the most common contaminants in the air pollutants. Inhalation exposure to PAHs could increase the risk of respiratory disease, cardiovascular disease and even cancer. However, the biotoxicity of multi-component PAHs from atmospheric pollutants has been poorly studies. The main topic of this study was to investigate the PAHs mixture, which derived from atmospheric pollutants, induced toxic effects and inflammatory effects on human bronchial epithelial cells in vitro. The results showed that PAHs mixture could decrease the cell viability, increase the apoptosis rate, and induce cell cycle arrest at S-phase. Furthermore, the expression of inflammatory factors IL-1ß and IL-6 were increased and NF-κB signaling pathway was activated in PAHs mixture-treated cells. The findings of this study indicate that PAHs mixture-induced cytotoxicity and inflammation may be related to intracellular ROS generation and to the activated NF-κB signaling pathway.
Subject(s)
Air Pollutants/toxicity , Bronchi/drug effects , Cytotoxins/toxicity , Epithelial Cells/drug effects , Polycyclic Aromatic Hydrocarbons/toxicity , Humans , Inflammation/chemically induced , Inhalation Exposure/adverse effectsABSTRACT
The quadratic polynomial fertilizer response model (QPFM) is the primary method for implementing quantitative fertilization in crop production, but the success rate of this model's recommended fertilization rates in China is low because the model contains a high setting bias. This paper discusses a new modelling method for expanding the applicability of QPFM. The results of field experiments with 8 levels of N, P, or K fertilization showed that the dynamic trend between rice yield increases and fertilizer application rate exhibited a typical exponential relationship. Therefore, we propose a unary non-structural fertilizer response model (NSFM). The responses of 18 rice field experiments to N, P, or K fertilization indicated that the new models could significantly predict rice yields, while two experimental fitting results using the unary QPFM did not pass statistical significance tests. The residual standard deviations of 13 new models were significantly lower than that of the unary QPFM. The linear correlation coefficient of the recommended application rates between the new model and the unary QPFM reached a significant level. Theoretical analysis showed that the unary QPFM was a simplified version of the new model, and it had a higher fitting precision and better applicability.
Subject(s)
Agriculture/methods , Fertilizers/analysis , Oryza/metabolism , Crop Production/methods , Crops, Agricultural/metabolism , Models, Theoretical , Nitrogen/analysis , Soil/chemistryABSTRACT
To study the gene expression change and possible signal pathway during androgen-dependent prostate cancer (ADPC) becoming androgen-independent prostate cancer (AIPC), an LNCaP cell model of AIPC was established using flutamide in combination with androgen-free environment inducement, and differential expression genes were screened by microarray. Then the biological process, molecular function and KEGG pathway of differential expression genes are analyzed by Molecule Annotation System (MAS). By comparison of 12,207 expression genes, 347 expression genes were acquired, of which 156 were up-ragulated and 191 down-regulated. After analyzing the biological process and molecule function of differential expression genes, these genes are found to play crucial roles in cell proliferation, differntiation, cell cycle control, protein metabolism and modification and other biological process, serve as signal molecules, enzymes, peptide hormones, cytokines, cytoskeletal proteins and adhesion molecules. The analysis of KEGG show that the relevant genes of AIPC transformation participate in glutathione metabolism, cell cycle, P53 signal pathway, cytochrome P450 metabolism, Hedgehog signal pathway, MAPK signal pathway, adipocytokines signal pathway, PPAR signal pathway, TGF-ß signal pathway and JAK-STAT signal pathway. In conclusion, during the process of ADPC becoming AIPC, it is not only one specific gene or pathway, but multiple genes and pathways that change. The findings above lay the foundation for study of AIPC mechanism and development of AIPC targeting drugs.
Subject(s)
Biomarkers, Tumor/genetics , Gene Expression Profiling , Neoplasms, Hormone-Dependent/genetics , Prostatic Neoplasms/genetics , Signal Transduction , Androgen Antagonists/pharmacology , Apoptosis , Cell Movement , Cell Proliferation , Flutamide/pharmacology , Gene Expression Regulation, Neoplastic , Humans , Male , Neoplasms, Hormone-Dependent/drug therapy , Neoplasms, Hormone-Dependent/pathology , Oligonucleotide Array Sequence Analysis , Prostatic Neoplasms/drug therapy , Prostatic Neoplasms/pathology , RNA, Messenger/genetics , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction , Tumor Cells, CulturedABSTRACT
Focal adhesion kinase (FAK), a nonreceptor tyrosine kinase protein, acts as an early modulator of integrin signaling cascade, regulating basic cellular functions. In transformed cells, unopposed FAK signaling has been considered to promote tumor growth, progression, and metastasis. The aim of this study was to assess the role of FAK in rat osteosarcoma OSR-6 cells. OSR-6 cells were transfected with PGPU6/GFP/shNC (shNC), and PGPU6/GFP/FAK-2434 (shRNA-2434), separately. Expression of FAK was detected by Real-time PCR and Western blots. MTT assay was used to examine changes in cell proliferation. Cell apoptosis was analyzed by flow cytometry. The expression of caspase-3,-7,-9 was measured by Western blots. The expression of FAK in OSR-6 cells significantly decreased in shRNA-2434 group in contrast to the control group (P < 0.01). Cell proliferation was inhibited by shRNA-2434 and shRNA-2434+ cisplatin, and the effects were clearly enhanced when cells were treated with anticancer agents. The level of cell apoptosis in shRNA-2434 and shRNA-2434+ cisplatin group was higher than that in the control group (P < 0.01). The current data support evidence that down-regulation of FAK could induce rat osteosarcoma cells (OSR-6) apoptosis through the caspase-dependent cell death pathway. Inhibition of the kinases may be important for therapies designed to enhance the apoptosis in osteosarcoma.
Subject(s)
Apoptosis , Caspase 3/metabolism , Caspases/metabolism , Down-Regulation , Focal Adhesion Protein-Tyrosine Kinases/genetics , Osteosarcoma/pathology , Signal Transduction , Animals , Apoptosis/drug effects , Apoptosis/genetics , Cell Line, Tumor , Cell Proliferation/drug effects , Cell Proliferation/genetics , Cisplatin/pharmacology , Down-Regulation/drug effects , Down-Regulation/genetics , Humans , RNA Interference , RNA, Small Interfering/genetics , Rats , Signal Transduction/drug effects , Signal Transduction/geneticsABSTRACT
A 2-year field experiment of mustard-cabbage-early rice rotation was conducted to investigate the effects of nitrogen application on yield and accumulation of nitrate nitrogen in the soil. The results showed that the applications of 150 kg N x hm(-2) for mustard and cabbage respectively and 90 kg N x hm(-2) for early rice were the best economic application mode, which could increase the net profit by 0.2%-75.6% compared with other application modes. Nitrogen application rates were positively correlated with NO3(-)-N concentration in the soil and in the percolating water. The vegetable-paddy rice rotation decreased the surplus of nitrogen in the soil. The average soil NO3(-)-N concentration was 29.7 mg x kg(-1) under the rotation of mustard-cabbage-early rice, which was only 84.4% of that under the continuous cropping of mustard-cabbage. The average NO3(-)-N concentration in the percolating water under mustard-cabbage-early rice rotation was little different from that in basal soil. Therefore, with the optimum nitrogen application mode, the vegetable-paddy rice rotation could gain the best economic benefit while significantly decrease the accumulation of nitrate nitrogen in the soil to effectively control non-point source pollution of nitrogen from vegetable fields.
Subject(s)
Agriculture/methods , Brassica/growth & development , Fertilizers , Nitrogen/analysis , Oryza/growth & development , Soil/chemistry , Nitrates , Nitrogen Cycle , VegetablesABSTRACT
The complete coding sequences of three of sheep genes SLC25A4, SLC25A5 and SLC25A6 were firstly amplified using the reverse transcriptase polymerase chain reaction (RT-PCR) according to the conserved sequence information of the cattle or other mammals and known highly homologous sheep ESTs. Sheep SLC25A4, SLC25A5 and SLC25A6 genes encode three corresponding proteins of 298 amino acids which contain the identically conserved putative mitochondrial carrier protein domain. Sheep SLC25A4 protein has high homology with the SLC25A4 proteins of six species-cattle (99%), human (95%), rat (95%), mouse (94%), dog (94%) and chicken (89%). Sheep SLC25A5 protein has high identity with the SLC25A5 proteins of five species-cattle (100%), dog (99%), mouse (98%), rat (98%) and human (98%). Sheep SLC25A6 protein also has high homology with the SLC25A6 proteins of four species-cattle (99%), human (97%), pig (97%) and chicken (93%). The phylogenetic tree analysis demonstrated that sheep SLC25A4, SLC25A5 and SLC25A6 proteins share a common ancestor. Moreover, SLC25A4, SLC25A5 and SLC25A6 proteins present stronger interaction each other. The tissue expression analysis indicated that sheep SLC25A4, SLC25A5 and SLC25A6 genes were expressed in a range of tissues including leg muscle, kidney, skin, longissimus dorsi muscle, spleen, heart and liver. Our experiment is the first to provide the primary foundation for further insight into these three sheep genes.