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1.
J Ethnopharmacol ; 331: 118332, 2024 Sep 15.
Article in English | MEDLINE | ID: mdl-38735421

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Citri Reticulata Pericarpium Viride (also known Qing-Pi or QP) is a plant in the Rutaceae family, QP is a traditional Qi-regulating medicine in Chinese medicine that is compatible with other Chinese medicine components and has extensive clinical practice in treating anxiety and depression. Reports on the pharmacological effects of QP have demonstrated its neuroprotective effects and antioxidant capacities. Numerous pharmacological benefits of QP are attributed to its antioxidant abilities. Anxiety disorders are a broadly defined category of mental illnesses. Oxidative stress and an imbalance in the antioxidant defense system are typical pathological features of these disorders. AIM OF THE STUDY: The aim of this study was to evaluate the effects of QP essential oil on anxiety using animal models and investigate the underlying neurobiological mechanisms. MATERIALS AND METHODS: This study aimed to develop an animal model of anxiety using chronic restraint stress and investigate the effects of inhalation of Citri Reticulata Pericarpium Viride essential oil on anxiety-like behavior, olfactory function, and olfactory bulb neurogenesis in mice with anxiety. RESULTS: The results showed that long-term chronic restraint stimulation caused a decrease in olfactory function, significant anxiety-like behavior, and a notable reduction in the number of neurons in the olfactory bulb. However, inhalation of Citri Reticulata Pericarpium Viride essential oil reversed these effects, improving the olfactory function, neuro-stimulating effect, alleviating anxiety-like behavior, and regulating theta (4-12Hz) oscillation in the hippocampus DG area. These effects were associated with changes in the expression levels of glutamate receptor NMDAR and NeuN in olfactory bulb. CONCLUSIONS: The study revealed that mice with anxiety induced by chronic restraint stress exhibited significant olfactory dysfunction, providing strong evidence for the causal relationship between anxiety disorders and olfactory dysfunction. Moreover, QP essential oil has the potential to be developed as a therapeutic drug for anxiety disorders, in addition to its role as a complementary anxiolytic.


Subject(s)
Anti-Anxiety Agents , Anxiety , Oils, Volatile , Olfactory Bulb , Receptors, N-Methyl-D-Aspartate , Animals , Oils, Volatile/pharmacology , Oils, Volatile/isolation & purification , Male , Anxiety/drug therapy , Mice , Anti-Anxiety Agents/pharmacology , Anti-Anxiety Agents/therapeutic use , Anti-Anxiety Agents/isolation & purification , Receptors, N-Methyl-D-Aspartate/metabolism , Behavior, Animal/drug effects , Glutamic Acid/metabolism , Neurogenesis/drug effects , Disease Models, Animal , Stress, Psychological/drug therapy
2.
Zhongguo Zhong Yao Za Zhi ; 49(2): 285-293, 2024 Jan.
Article in Chinese | MEDLINE | ID: mdl-38403304

ABSTRACT

The 21st century is a highly information-driven era, and traditional Chinese medicine(TCM) pharmacy is also moving towards digitization and informatization. New technologies such as artificial intelligence and big data with information technology as the core are being integrated into various aspects of drug research, manufacturing, evaluation, and application, promoting interaction between these stages and improving the quality and efficiency of TCM preparations. This, in turn, provides better healthcare services to the general population. The deep integration of emerging technologies such as artificial intelligence, big data, and cloud computing with the TCM pharmaceutical industry will innovate TCM pharmaceutical technology, accelerate the research and industrialization process of TCM pharmacy, provide cutting-edge technological support to the global scientific community, boost the efficiency of the TCM industry, and promote economic and social development. Drawing from recent developments in TCM pharmacy in China, this paper discussed the current research status and future trends in digital TCM pharmacy, aiming to provide a reference for future research in this field.


Subject(s)
Drugs, Chinese Herbal , Pharmacy , Humans , Medicine, Chinese Traditional , Artificial Intelligence , Technology, Pharmaceutical , Drug Industry
3.
Article in English | MEDLINE | ID: mdl-38193238

ABSTRACT

This paper extends a text classification method utilizing natural language processing (NLP) into the field of traditional Chinese medicine (TCM) compound decoction to effectively and scientifically extend the TCM compound decoction duration. Specifically, a TCM compound decoction duration classification named TCM-TextCNN is proposed to fuse multi-dimensional herb features and improve TextCNN. Indeed, first, we utilize word vector technology to construct feature vectors of herb names and medicinal parts, aiming to describe the herb characteristics comprehensively. Second, considering the impact of different herb features on the decoction duration, we use an improved Term Frequency-Inverse Word Frequency (TF-IWF) algorithm to weigh the feature vectors of herb names and medicinal parts. These weighted feature vectors are then concatenated to obtain a multi-dimensional herb feature vector, allowing for a more comprehensive representation. Finally, the feature vector is input into the improved TextCNN, which uses k-max pooling to reduce information loss rather than max pooling. Three fully connected layers are added to generate higher-level feature representations, followed by softmax to obtain the final results. Experimental results on a dataset of TCM compound decoction duration demonstrate that TCM-TextCNN improves accuracy, recall, and F1 score by 5.31%, 5.63%, and 5.22%, respectively, compared to methods solely rely on herb name features, thereby confirming our method's effectiveness in classifying TCM compound decoction duration.

4.
Anal Chem ; 95(49): 17968-17973, 2023 12 12.
Article in English | MEDLINE | ID: mdl-38032052

ABSTRACT

Extracellular vesicles (EVs) are used by living cells for the purpose of biological information trafficking from parental-to-recipient cells and vice versa. This back-and-forth communication is enabled by two distinct kinds of biomolecules that constitute the cargo of an EV: proteins and nucleic acids. The proteomic-cum-genetic information is mediated by the physiological state of a cell (healthy or otherwise) as much as modulated by the biogenesis pathway of the EV. Therefore, in mirroring the huge diversities of human communications, the proteins and nucleic acids involved in cell communications possess seemingly near limitless diversities, and it is this characteristic that makes EVs so highly heterogeneous. Currently, there is no simple and reliable tool for the selective capture of heterogeneous EVs and the delivery of their undamaged cargo for research in extracellular protein mapping and spatial proteomics studies. Our work is a preliminary attempt to address this issue. We demonstrated our approach by using antibody functionalized liposomes to capture EVs from tumor and healthy cell-lines. To characterize their performance, we presented fluorescence and nanoparticle tracking analysis (NTA) results, TEM images, and Western blotting analysis for EV proteins. We also extracted dermal interstitial fluid (ISF) from healthy individuals and used our functionalized synthetic vesicle (FSV) method to capture EVs from their proteins. We constructed three proteomic sets [EV vs ISF, (FSV+EV) vs ISF, and (FSV+EV) vs EV] from the EV proteins and the free proteins harvested from ISF and compared their differentially expressed proteins (DEPs). The performance of our proposed method is assessed via an analysis of 1095 proteins, together with volcano plots, heatmap, GO annotation, and enriched KEGG pathways and organelle localization results of 213 DEPs.


Subject(s)
Extracellular Vesicles , Nucleic Acids , Humans , Liposomes/metabolism , Extracellular Fluid , Proteomics/methods , Extracellular Vesicles/metabolism , Nucleic Acids/metabolism
5.
Fitoterapia ; 169: 105583, 2023 Sep.
Article in English | MEDLINE | ID: mdl-37336418

ABSTRACT

Phytochemical investigation of the volatile oil of Yueju (YJVO) and its constituent herbs induced the detection of 52 compounds in YJVO, mainly monoterpenes and sesquiterpenes as well as a small amount of aromatic and aliphatic compounds. 5 of these compounds were found only in the YJVO instead of the volatile oil of its constituent herbs. The anti-depressant effect of YJVO was proved by behavioral tests in chronic unpredictable mild stress (CUMS) mice. An acute oral toxicity evaluation determined the LD50 of YJVO was 5.780 mL/kg. Doppler ultrasound and laser speckle imaging have detected that the YJVO could improve depression-related cerebral blood flow. In addition, related neurotransmitters and proteins were analyzed through targeted metabolomics and immunofluorescence. The potential antidepressant mechanisms of YJVO related to significantly decreasing Glu in CUMS mice by up-regulating the ERK/AKT-mediated expression of GLT-1.


Subject(s)
Depression , Oils, Volatile , Mice , Animals , Depression/drug therapy , Glutamic Acid/metabolism , Proto-Oncogene Proteins c-akt/metabolism , Oils, Volatile/pharmacology , Molecular Structure , Antidepressive Agents/pharmacology , Stress, Psychological/metabolism , Disease Models, Animal , Hippocampus
6.
Phytomedicine ; 116: 154852, 2023 Jul 25.
Article in English | MEDLINE | ID: mdl-37167824

ABSTRACT

BACKGROUND: Current antidepressant therapy remains unsatisfactory due to the complex pathogenesis. Emerging evidence suggested that depression is associated with inflammatory bowel disease (IBD), intestinal inflammation is an increasingly accepted factor that influences depression, but the mechanism is unclear. PURPOSE: In the current study, we determined whether Pulsatilla chinensis saponins (PRS), a phytomedicine from Pulsatilla chinensis (Bunge) Regel with excellent anti-IBD effect, could improve the depression. Furthermore, we investigated the mechanisms to explore the relationship between IBD and depression and provide new source for the urgent development of antidepressants from phytomedicine. METHODS: The antidepressant activity of PRS was accessed by behavioral test and multichannel technology in depression mice induced by Chronic Unpredictable Mild Stress (CUMS). 16S rDNA-based microbiota and RNA-seq in colon was used to explore potential intestinal metabolism affected by PRS. To illustrate the underlying mechanisms of anti-depression effect of PRS, targeted metabolomics, ELISA assay, immunofluorescence staining, Western Blot, and qPCR were carried out. RESULTS: The results clarified that CUMS induced depression with tryptophan (Trp) metabolism and intestinal inflammation. PRS effectively suppressed the depression and acted as a regulator of Trp/kynurenine (Kyn) metabolic and intestinal inflammation confirmed by analysis of microflora and colon RNA. Meanwhile PRS reduced interferon gamma (IFN-γ), inhibited JAK1-STAT1 phosphorylation, decreased IDO1 levels to protect against the overactivity of Trp/kyn path, suggesting that IFN-γ activated IDO1 probably a significant target for PRS to exert anti-depression effects. To further confirm the mechanism, this research expressed that PRS improved IDO1 activity and depressive behavior in mice with IFN-γ-induced depression. Furthermore, the therapeutic effect of 1-methyl-tryptophan (1-MT) well known as an IDO1 inhibitor in depression and clinically used anti-UC drug Mesalazine (MS) was demonstrated to confirm the potential mechanism. CONCLUSION: The study is the first to reveal the antidepressant effect of PRS and further demonstrate its potential therapeutic targets. In addition, it also clarifies that the Trp/kyn pathway is the crosstalk between IBD and depression and provides new choice for depression treatment. And it also provides an important basis for the follow-up development and exploration of anti-intestinal antidepressants.


Subject(s)
Inflammatory Bowel Diseases , Pulsatilla , Saponins , Mice , Animals , Tryptophan , Saponins/pharmacology , Antidepressive Agents/pharmacology , Interferon-gamma , Inflammation/drug therapy , Indoleamine-Pyrrole 2,3,-Dioxygenase/metabolism
7.
Zhongguo Zhong Yao Za Zhi ; 48(6): 1438-1445, 2023 Mar.
Article in Chinese | MEDLINE | ID: mdl-37005831

ABSTRACT

As an important model animal, fruit fly is characterized by outstanding genetic characteristics, relatively perfect nervous system, rapid reproduction, and low cost. Thus, it has been applied in the research on neuropsychiatric disorders in recent years, showing great potential in life science. The incidence of neuropsychiatric disorders has been on the rise, and the disorders have high disability rate and low case fatality rate. The global drug demand for such diseases is second only to cardiovascular and cerebrovascular diseases. At the moment, the demand of the drugs for the diseases have been rising, and it is an urgent task to develop related drugs. However, the research and development of the drugs are time-intensive and have a high failure rate. A suitable animal model can help shorten the time for drug screening and development, thereby reducing the cost and failure rate. This study reviews the application of fruit flies in several common neuropsychiatric disorders, which is expected to provide new ideas for the research and application of the model animals in traditional Chinese medicine.


Subject(s)
Cerebrovascular Disorders , Drugs, Chinese Herbal , Animals , Medicine, Chinese Traditional , Drugs, Chinese Herbal/pharmacology , Drugs, Chinese Herbal/therapeutic use , Models, Animal
8.
J Ethnopharmacol ; 308: 116215, 2023 May 23.
Article in English | MEDLINE | ID: mdl-36806339

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Pulsatilla decoction has been extensively used to treat ulcerative colitis (UC) in recent years. Pulsatilla chinensis saponin (PRS), the active ingredient of its monarch medicine Pulsatilla chinensis (Bunge) Regel, plays a crucial role in the treatment of UC, but its specific mechanism of action has not been fully elucidated. AIM OF THE STUDY: This study aims to investigate the protective effect and possible mechanism of PRS on DSS-induced ulcerative colitis in rats. MATERIALS AND METHODS: In this study, the DSS-induced colitis model was used to explore the metabolism and absorption of PRS under UC, detect the content of short-chain fatty acids (SCFAs) in colon tissue, the expression of receptor G Protein-Coupled Receptor 43 (GPR43) protein and inflammasome NLRP3, and observe the expression level of IL-1ß, IL-6 and TNF-α in colon tissue. The protective effect of the PRS was also observed. RESULTS: It was found that in the UC group, the absorption rate and extent of drugs increased, and the elimination was accelerated. Compared with the control group, PRS increased the content of short-chain fatty acids (SCFAs) in colon tissue, promoted the expression of SCFAs receptor GPR43 protein, inhibited the activation of the NLRP3 inflammasome, and decreased the content of IL-1ß, IL-6 and TNF-α. PRS protects the colon in DSS-induced inflammatory bowel disease by increasing the content of SCFAs, promoting the expression of GPR43 protein, inhibiting the activation of the NLRP3 inflammasome, and reversing the increase in IL-1ß, IL-6 and TNF-α levels. CONCLUSIONS: PRS can increase the content of colonic SCFAs, activate the GPR43-NLRP3 signaling pathway, and reduce the levels of pro-inflammatory cytokines, thereby improving the symptoms of DSS-induced colitis.


Subject(s)
Colitis, Ulcerative , Colitis , Pulsatilla , Saponins , Rats , Animals , Mice , Colitis, Ulcerative/drug therapy , NLR Family, Pyrin Domain-Containing 3 Protein/metabolism , Inflammasomes/metabolism , Tumor Necrosis Factor-alpha/metabolism , Saponins/pharmacology , Interleukin-6/metabolism , Colitis/drug therapy , Colon , Signal Transduction , Receptors, G-Protein-Coupled/metabolism , Fatty Acids, Volatile/metabolism , Dextran Sulfate , Mice, Inbred C57BL , Disease Models, Animal
9.
Chem Biodivers ; 19(9): e202100961, 2022 Sep.
Article in English | MEDLINE | ID: mdl-35979749

ABSTRACT

Herba Patriniae (HP) is widely used as a medicinal and edible material in China. Besides food value, HP attracts more attention due to its medicinal potential. Patrinia villosa Juss. (PV) and Patrinia scabiosaefolia Fisch. (PS) are the two species origins of HP. These two of HP show different effects on cell proliferation, migration, angiogenesis and anti-diabetic. As we have previously reported, PV and PS show significant differences on their anti-inflammatory ability in the same experimental model. Comparing the ingredient profiles of two different sources will not only facilitate the understanding of their medicinal effects, but also help the development and research of new activities. However, still now, there is no systematic and detailed study to compare the components of PV and PS. In present study, ultra-high performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry was employed to achieve a high-throughput qualitative and thorough analysis of the chemical composition spectrum of HP. A total of 164 compounds were identified, among these compounds, 127 compounds were identified from PV, and 107 compounds were identified from PS. Most of the chemical components was discovered for the first time. Flavonoids, saponins, terpenoids and organic acids, as the main ingredients in PV and PS were 45.45 %vs 28.46 %, 12.61 % vs. 32.09 %, 14.33 % vs. 22.38 % and 14.58 % vs. 6.79 %, respectively. Flavonoids are the main components of PV, while PS is rich in saponins. PV and PS were classified into two groups by principal component analysis (PCA) and screened out the main molecular differences responsible by orthogonal partial least squares discriminant analysis (OPLS-DA). All the results will be a guide for the quality control, functional activity research, or better clinic use based on the ingredients profile between these two species. Besides, this first study on ingredients profile of two species origins will be beneficial for potential and best resources utilization of both PV and PS.


Subject(s)
Patrinia , Saponins , Anti-Inflammatory Agents/pharmacology , Chromatography, High Pressure Liquid/methods , Discriminant Analysis , Flavonoids/chemistry , Least-Squares Analysis , Patrinia/chemistry , Tandem Mass Spectrometry/methods , Terpenes
10.
Food Sci Nutr ; 10(1): 49-59, 2022 Jan.
Article in English | MEDLINE | ID: mdl-35035908

ABSTRACT

Schisandra chinensis (S. chinensis) extract powder is an important intermediate for the preparation of many prepared medicines and health products. The physicochemical properties of S. chinensis extract powder have been found to vary tremendously and this has been attributed to the long drying time in the traditional drying method. In this study, S. chinensis specimens were authenticated as the dry fruit of S. chinensis (Turcz.) Baill. S. chinensis were extracted twice with 8 L kg-1 (liquid to solid ratio) distilled water. The extracts were mixed and concentrated under reduced pressure to 1.24 g cm-3. Ultrasound-assisted vacuum drying (UAVD) was employed as a new approach to improve the efficiency in drying S. chinensis extract powder and produce a higher quality product. The effects of drying temperature (70, 80, 90°C), ultrasonic power (40, 120, 200 W), and ultrasonic application time (4, 12, 20 min every 20 min) on the kinetics and quality of S. chinensis extract were investigated and compared with the conventional vacuum drying (CVD). It was shown that, with the increase in drying temperature, ultrasonic power, and time of UAVD, the drying time for S. chinensis extract to reach the equilibrium moisture decreased. The drying time was reduced by more than 25% when utilizing UAVD compared to the CVD method. The effective moisture diffusivity (D eff) values for CVD and UAVD were 3.48 × 10-9 m2·s-1 and 7.41 × 10-9 m2 s-1, respectively, at the drying temperature of 80°C, indicating an increase of 112.93%. It was also found that a Weibull distribution model was suitable for predicting the moisture content of S. chinensis extract (R 2 > 0.95). Furthermore, the content of Schisandrol A in the extracts obtained from UAVD was 12.79% higher than that obtained using CVD at 90°C. This demonstrates that UAVD is an efficient drying technique for S. chinensis extract.

11.
Planta Med ; 88(14): 1311-1324, 2022 Nov.
Article in English | MEDLINE | ID: mdl-34911135

ABSTRACT

Clinical studies have shown that insomnia and anxiety are usually accompanied by cardiovascular dysfunction. In traditional Chinese medicine, Schisandra chinensis (SC) and wine processed Schisandra chinensis (WSC) are mainly used for the treatment of dysphoria, palpitation and insomnia. However, little attention was paid to its mechanism. In this study, we monitored the effect of SC and WSC on the nervous system and cardiovascular system of free-moving rats in the real-time. Our results show that SC and WSC can alleviate cardiovascular dysfunction while promoting sleep, and we further explored their potential mechanisms. HPLC-QTOF-MS was used for the quality control of chemical components in SC and WSC. Data sciences international (DSI) physiological telemetry system was applied to collect the electroencephalogram (EEG), electrocardiogram (ECG) and other parameters of free-moving rats to understand the effects of long-term intake of SC and WSC on rats. The content of Cortisol (CORT), neurotransmitters and amino acids in rat pituitary and hypothalamus were analyzed by UPLC-MS to determine the activity of HPA axis. The expression of melatonin receptor MT1 was analyzed by immunofluorescence technique. Our results suggested that SC and WSC may play the role of promoting sleep by increasing the expression level of melatonin receptor MT1 in hypothalamus, and modulate the activity of HPA axis by regulating the levels of the related neurotransmitters and amino acid, so as to improve the abnormal cardiovascular system of rats. This study may provide theoretical support for explicating the advantages of SC and other phytomedicines in the treatment of insomnia.


Subject(s)
Schisandra , Sleep Initiation and Maintenance Disorders , Wine , Animals , Rats , Schisandra/chemistry , Schisandra/metabolism , Sleep Initiation and Maintenance Disorders/drug therapy , Receptors, Melatonin/metabolism , Chromatography, Liquid , Hypothalamo-Hypophyseal System/metabolism , Tandem Mass Spectrometry/methods , Rats, Sprague-Dawley , Pituitary-Adrenal System/metabolism , Neurotransmitter Agents/metabolism , Amino Acids , Sleep
12.
Phytomedicine ; 94: 153833, 2022 Jan.
Article in English | MEDLINE | ID: mdl-34798520

ABSTRACT

BACKGROUND: Atherosclerosis (AS) is a multifactor cardiovascular disease characterized by chronic inflammation. The safety of long-term medication is the focus of clinical treatment selection and application. It is urgent to develop more high-efficiency and low side effects drugs to treat AS. Therefore, the screening of anti-AS drugs with high efficiency and low toxicity from phytomedicine has attracted more and more attention. PURPOSE: The aim of this study was to explore the new pharmacological effect of Herba patriniae against AS, to find the best origin and extraction part of Herba patriniae, furthermore, to reveal its potential action mechanism. METHODS: Apolipoprotein E gene-knockout (ApoE-/-) mice were orally administered with different extracts of Patrinia villosa Juss (PVJ) and Patrinia scabiosaefolia Fisch (PSF). Their anti-AS effect was comprehensively evaluated by small animal ultrasound, HE staining, Oil-Red O staining, platelet aggregation rate and blood lipid level. Lipid metabolomics and network pharmacology were used to study the mechanism of drug action. Finally, the expression of related proteins were detected by western blots and immunofluorescence. RESULTS: PVJ EtOAc extract and PSF EtOAc extract could significantly reduce vascular plaque, liver inflammation, platelet aggregation and blood lipid levels in AS model. By comparison, the effect of PVJEE was better than that of PSFEE. Furthermore, the results of differential metabolites indicated that PVJEE may inhibit the apoptosis of vascular endothelial cells, proliferation and migration of smooth muscle cells by reversing lysophosphatidylcholine (LPC) in the glycerophospholipid metabolic pathway, so as to play an anti-AS role. This result was double verified by KEGG based metabolic pathway enrichment analysis and related protein expression study. CONCLUSION: By changing glycerophospholipid metabolism pathway, Herba patriniae can significantly regulate lipid metabolism and inflammatory level, showing the development potential of anti-AS, which provides new candidate drugs and good prospects for the safe treatment of AS. In addition, through comparison, this study also confirmed that PVJEE was the best origin and extraction part of anti-AS.


Subject(s)
Atherosclerosis , Lysophosphatidylcholines , Animals , Atherosclerosis/drug therapy , Endothelial Cells , Glycerophospholipids , Mice
13.
Exp Neurobiol ; 30(6): 387-400, 2021 12 31.
Article in English | MEDLINE | ID: mdl-34983880

ABSTRACT

Insomnia has become a common central nervous system disease. At present, the pathogenesis of insomnia is not clear. Animal models can help us understand the pathogenesis of the disease and can be used in transformational medicine. Therefore, it is very necessary to establish an appropriate model of insomnia. Clinical data show that insomnia patients with high levels of thyroxine and often accompanied by cardiovascular problems, a common mechanism underlying all of these physiological disruptions is the sympathetic nervous system. Combined with the characteristics of chronic onset of clinical insomnia, an insomnia model induced by long-term intraperitoneal injection of thyroid hormone has been created in our laboratory. In this paper, the insomnia-like state of the model was evaluated based on three validity criteria. Face validity has been demonstrated in metabolism, the Morris water maze, electrocardiogram (ECG) and electroencephalogram (EEG). Structure validity has been proved by the results of targeted metabolomics. After treatment with diazepam, a commonly used clinical anti-insomnia drug, the above physiological and pathological disorders were reversed. The results of comprehensive analysis show that the established thyrotoxicosis-associated insomnia model meets the validity requirement to establish an appropriate animal model of insomnia. The model presented in this article might help to study pathogenetic mechanisms of clinical insomnia, as well as to test promising methods of insomnia treatment.

14.
Zhongguo Zhong Yao Za Zhi ; 43(5): 959-963, 2018 Mar.
Article in Chinese | MEDLINE | ID: mdl-29676094

ABSTRACT

A new sesquiterpenes named glaucochinarol A (1) and a new phenylpropane glycoside named glcacochinaside A (2), together with six known ones, including trichothecolone (3), ß-D-(6-O-trans-feruloyl)fructofuranosyl-α-D-O-glucopyranoisde (4), 3,4,5-trimethoxyphenyl-ß-D-glucopyranoside (5), (4R)-p-menth-1-ene-7,8-diol-7-O-ß-D-glucopyranoside (6), naringenin (7), and emodin-8-O-ß-glucoside (8) were isolated from smilax glaucochina warb. Their structures were elucidated on the basis of NMR, MS and published data. Compounds 3-8 were isolated from the species for this first time.


Subject(s)
Glycosides/chemistry , Sesquiterpenes/chemistry , Smilax/chemistry , Glycosides/isolation & purification , Magnetic Resonance Spectroscopy , Molecular Structure , Phytochemicals/chemistry , Phytochemicals/isolation & purification , Sesquiterpenes/isolation & purification
15.
Nat Prod Res ; 32(15): 1760-1768, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29149807

ABSTRACT

Three new flavonoid glycosides, 2(S)-5-hydroxy-6,8-dimethoxyflavonone-7-O-ß-D-glucopyranosyl-(1→6)-O-ß-D-glucopyranoside (1), 5-hydroxy-3,8-dimethoxyflavone-7-O-ß-D-glucopyranosyl-(1→6)-O-ß-D-glucopyranoside (2) and 3,7-dihydroxy-8-methoxyflavone-6-O-ß-D-glucopyranosyl-(1→6)-O-ß-D-glucopyranoside (3), together with five known flavonoids (4-8) were isolated from the roots of Smilax glabra Roxb. Their structures were elucidated on the basis of chemical and spectral evidence, as well as by comparison with literature data. Three new flavonoids were subjected to evaluate anti-inflammatory activity. Compounds 1-3 inhibited the NF κB induction by 32.2, 55.8 and 61.7%, respectively.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Flavonoids/pharmacology , Glycosides/pharmacology , Smilax/chemistry , Animals , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Cell Line , Drug Evaluation, Preclinical , Flavonoids/chemistry , Glycosides/chemistry , Magnetic Resonance Spectroscopy , Molecular Structure , NF-kappa B/antagonists & inhibitors , Plant Roots/chemistry , Spectrometry, Mass, Electrospray Ionization
16.
J Asian Nat Prod Res ; 19(8): 754-765, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28276765

ABSTRACT

Six new steroidal saponins, namely glauco-chinaosides A-F, and one known compound were isolated from the tubers of Smilax glauco-china. Their structures were elucidated by a combination of spectroscopic analysis and hydrolysis followed by spectral and chromatographic analysis. Compounds 1-7 were tested in vitro for their cytotoxic activities against four human tumor cell lines (SH-SY5Y, SGC-7901, HCT-116, and Lovo). Compounds 1, 2, and 5 exhibited cytotoxic activity against SGC-7901, with IC50 values of 2.7, 11.5, and 6.8 µM, respectively.


Subject(s)
Antineoplastic Agents, Phytogenic/isolation & purification , Antineoplastic Agents, Phytogenic/pharmacology , Drugs, Chinese Herbal/isolation & purification , Drugs, Chinese Herbal/pharmacology , Glycosides/isolation & purification , Glycosides/pharmacology , Saponins/isolation & purification , Saponins/pharmacology , Smilax/chemistry , Sterols/isolation & purification , Sterols/pharmacology , Antineoplastic Agents, Phytogenic/chemistry , Drug Screening Assays, Antitumor , Drugs, Chinese Herbal/chemistry , Glycosides/chemistry , HCT116 Cells , Humans , Inhibitory Concentration 50 , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Rhizome/chemistry , Saponins/chemistry , Sterols/chemistry
17.
Zhong Yao Cai ; 39(4): 782-5, 2016 Apr.
Article in Chinese | MEDLINE | ID: mdl-30132319

ABSTRACT

Objective: To study the phenylpropanoid constituents of Smilax trinervula. Methods: The chemical constituents were isolated and purified by macroporous adsorption resin chromatography, gel chromatography and high performance liquid chromatography. Their structures were identified by spectroscopic analysis and comparison with literatures. Results: Nine phenylpropanoid compounds were isolated and their structures were identified as( +)-lyoniresin-4-yl ß-D-glucopyranoside( 1),(-)-8'-epilyoniresin-4-yl ß-glucopyranoside( 2),( +)-lyoniresin-4'-yl ß-glucopyranoside( 3),(-)-lyoniresinol-2α-O-ß-D-glucopyranoside( 4),( +)-lyoniresinol( 5),icariol A2( 6),icariol A2-4-O-ß-D-glucopyranoside( 7),7S,7'S,8R,8'R-icariol A2-9-O-ß-D-glucopyranoside( 8) and( +)-syringaresinol-4'-O-ß-D-glucopyranoside( 9). Conclusion: All the compounds are isolated from Smilax genus for the first time.


Subject(s)
Smilax , 1-Propanol , Chromatography, High Pressure Liquid , Drugs, Chinese Herbal , Furans , Lignans , Plant Extracts
18.
Zhongguo Zhong Yao Za Zhi ; 41(3): 446-450, 2016 Feb.
Article in Chinese | MEDLINE | ID: mdl-28868862

ABSTRACT

The chemical constituents were separated and purified from the 70% ethanol extract of Smilax trinervulaby various chromatographic methods including silica gel, Sephadex LH-20, MCI and preparative HPLC. Their structures were obtained and identified by analysis of the spectroscopic data. Compounds 1-11 were separated from this genus for the first time. Compound 12 was obtained from S. trinervula for the first time.


Subject(s)
Drugs, Chinese Herbal/chemistry , Smilax/chemistry , Chromatography, High Pressure Liquid , Drugs, Chinese Herbal/isolation & purification , Mass Spectrometry , Molecular Structure , Rhizome/chemistry
19.
Oncol Res Treat ; 37(4): 164-9, 2014.
Article in English | MEDLINE | ID: mdl-24732639

ABSTRACT

BACKGROUND: Glutathione S-transferase (GST) T1 and M1 are detoxification enzymes which neutralize various carcinogenic compounds. Polymorphisms of the GSTT1 and GSTM1 genes which encode the enzymes could be associated with cancer risk. PATIENTS AND METHODS: We investigated the association of GSTT1 and GSTM1 null polymorphisms with lung cancer risk in a tightly matched, considerably large sample in China. Genotyping was performed utilizing polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis and DNA sequencing, and associations were measured by using logistic regression analysis. RESULTS: We found that the null genotypes of both polymorphisms resulted in an increased lung cancer risk, with an odds ratio (OR) of 1.57 (95% confidence interval (CI) 1.23-2.00) for GSTT1 and OR 1.87 (95% CI 1.46-2.39) for GSTM1 (p < 0.01). Significant associations remained after stratification by histopathology (p < 0.01) and smoking status (p < 0.05). When gender-stratified association was performed, we found that the GSTT1 null genotype resulted in an increased risk among males (adjusted OR 2.95, 95% CI 2.07-4.20; p < 0.01) but not females (p > 0.05), while the GSTM1 null genotype resulted in an increased risk among females (adjusted OR 2.18, 95% CI 1.54-3.10; p < 0.01) but not males (p < 0.05). CONCLUSION: Polymorphisms in GSTT1 and GSTM1 are associated with the risk of lung cancer in a gender-specific manner.


Subject(s)
Biomarkers, Tumor/genetics , Genetic Predisposition to Disease/epidemiology , Genetic Predisposition to Disease/genetics , Glutathione Transferase/genetics , Lung Neoplasms/epidemiology , Lung Neoplasms/genetics , Adult , Aged , Base Sequence , China/epidemiology , Female , Genetic Markers/genetics , Humans , Male , Middle Aged , Polymorphism, Single Nucleotide/genetics , Prevalence , Risk Factors , Sex Distribution , Sex Factors
20.
J Chromatogr A ; 1321: 21-9, 2013 Dec 20.
Article in English | MEDLINE | ID: mdl-24238713

ABSTRACT

A novel type of magnetic nanoparticles, 3-fluorobenzoyl chloride functionalized magnetic nanoparticles (Fe3O4@SiO2@FBC MNPs) was successfully synthesized. It was applied to the extraction and determination of perfluorinated compounds (PFCs) by coupling with ultra-high performance liquid chromatography with tandem triple quadrupole mass spectrometry (UHPLC-MS/MS). Due to the fluorous-fluorous interaction, the magnetic nanoparticles displayed excellent extraction performance for 6 PFCs, including perfluoroheptanoic acid (PFHpA), perfluorodecanoic acid (PFDA), perfluorododecanoic acid (PFDoA), perfluorotetradecanoic acid (PFTeDA), perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS). The UHPLC separation of PFCs was very quick and could be achieved within 6min. Various factors that may influence the magnetic solid-phase extraction (MSPE) efficiency, such as sorbent amount, desorption solvent, extraction time, pH value of water samples and sample volume, were investigated in detail. Under the optimum conditions, the linear ranges of six PFCs were 0.25-25ng/L with the limits of detection (S/N=3) ranging from 0.01 to 0.06ng/L. Finally, the method was successfully applied to different river water samples, and the recoveries were in the range of 89.34-111.32%. These results indicated that the prepared Fe3O4@SiO2@FBC sorbents could efficiently enrich PFCs and that the proposed method is reliable.


Subject(s)
Benzoates/chemical synthesis , Magnetics , Rivers , Water Pollutants, Chemical/isolation & purification , Adsorption , Benzoates/chemistry , Chromatography, High Pressure Liquid , Hydrogen-Ion Concentration , Microscopy, Electron, Transmission , Spectroscopy, Fourier Transform Infrared , Tandem Mass Spectrometry
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