1.Schisandrin B Inhibits NLRP3 Inflammasome Pathway and Attenuates Early Brain Injury in Rats of Subarachnoid Hemorrhage.
Song CHEN ; Yi-Hang DING ; Song-Sheng SHI ; Xian-Kun TU
Chinese journal of integrative medicine 2022;28(7):594-602
OBJECTIVE:
To determine whether Schisandrin B (Sch B) attenuates early brain injury (EBI) in rats with subarachnoid hemorrhage (SAH).
METHODS:
Sprague-Dawley rats were divided into sham (sham operation), SAH, SAH+vehicle, and SAH+Sch B groups using a random number table. Rats underwent SAH by endovascular perforation and received Sch B (100 mg/kg) or normal saline after 2 and 12 h of SAH. SAH grading, neurological scores, brain water content, Evan's blue extravasation, and terminal transferase-mediated dUTP nick end-labeling (TUNEL) staining were carried out 24 h after SAH. Immunofluorescent staining was performed to detect the expressions of ionized calcium binding adapter molecule 1 (Iba-1) and myeloperoxidase (MPO) in the rat brain, while the expressions of B-cell lymphoma 2 (Bcl-2), Bax, Caspase-3, nucleotide-binding oligomerization domain-like receptor family pyrin domain-containing 3 (NLRP3), apoptosis-associated specklike protein containing the caspase-1 activator domain (ASC), Caspase-1, interleukin (IL)-1β, and IL-18 in the rat brains were detected by Western blot.
RESULTS:
Compared with the SAH group, Sch B significantly improved the neurological function, reduced brain water content, Evan's blue content, and apoptotic cells number in the brain of rats (P<0.05 or P<0.01). Moreover, Sch B decreased SAH-induced expressions of Iba-1 and MPO (P<0.01). SAH caused the elevated expressions of Bax, Caspase-3, NLRP3, ASC, Caspase-1, IL-1β, and IL-18 in the rat brain (P<0.01), all of which were inhibited by Sch B (P<0.01). In addition, Sch B increased the Bcl-2 expression (P<0.01).
CONCLUSION
Sch B attenuated SAH-induced EBI, which might be associated with the inhibition of neuroinflammation, neuronal apoptosis, and the NLRP3 inflammatory signaling pathway.
Animals
;
Apoptosis
;
Brain/pathology*
;
Brain Injuries/pathology*
;
Caspase 3/metabolism*
;
Cyclooctanes
;
Evans Blue
;
Inflammasomes/metabolism*
;
Interleukin-18/metabolism*
;
Lignans
;
NLR Family, Pyrin Domain-Containing 3 Protein/metabolism*
;
Polycyclic Compounds
;
Proto-Oncogene Proteins c-bcl-2/metabolism*
;
Rats
;
Rats, Sprague-Dawley
;
Subarachnoid Hemorrhage/drug therapy*
;
Water
;
bcl-2-Associated X Protein/metabolism*
2.Preparation and evaluation of schisandrin B-loaded F127 modified lipid-polymer nanoparticles for inhibition of breast cancer lung metastasis.
Fei YAN ; Jiang-Pei SHI ; Hai-Zhen CHEN ; Jun-Yi SHEN ; Xing-Mei XIE ; Zi-Fei JIANG ; G U XIAO-YAN ; Ying LIU ; Nian-Ping FENG
China Journal of Chinese Materia Medica 2020;45(21):5177-5183
In the current study, schisandrin B(SchB)-loaded F127 modified lipid-polymer hybrid nanoparticles(SchB-F-LPNs) were developed to improve the inhibition of breast cancer lung metastasis. Modified nanoprecipitation method was used to prepare SchB-F-LPNs. The nanoparticles were spherical in shape with shell-core structure by TEM observation. SchB-F-LPNs showed a mean particle size of(234.60±6.11) nm with zeta potential of(-5.88±0.49) mV. XRD results indicated that SchB existed in the nanoparticles in an amorphous state. The apparent permeability coefficient through porcine mucus of F-LPNs was 1.43-fold of that of LPNs as shown in the in vitro mucus penetration study. The pharmacokinetics study showed that the C_(max) of SchB was(369.06±146.94) μg·L~(-1),(1 121.34±91.65) μg·L~(-1) and(2 951.91±360.53) μg·L~(-1) respectively in SchB suspensions group, SchB-LPNs group and SchB-F-LPNs group after oral administration in rats. With SchB suspensions as the reference formulation, the relative bioavailability of SchB-F-LPNs was 568.60%. SchB-F-LPNs inhibited the morphological change during transforming growth factor-β1(TGF-β1)-induced epithelial-mesenchymal transition. In addition, SchB-F-LPNs significantly decreased the number of metastatic pulmonary nodules in 4 T1 tumor-bearing mice, suggesting that SchB-F-LPNs may inhibit the metastasis of breast cancer. These results reveal the promising potential of SchB-F-LPNs in treatment of breast cancer lung metastasis.
Animals
;
Cyclooctanes
;
Lignans
;
Lipids
;
Lung Neoplasms/drug therapy*
;
Mice
;
Nanoparticles
;
Polycyclic Compounds
;
Polyethylenes
;
Polymers
;
Polypropylenes
;
Rats
;
Swine
3.The exposure level of environmental harmful substances related to the secondhand smoke in Korean non-smoker adults: data from the second Korean National Environmental Health Survey (KoNEHS 2012–2014): a cross-sectional study
Sang Woo KIM ; Sung Won JUNG ; Jae Gwang LEE ; Jae Han JOO ; June Hee LEE ; Kyung Jae LEE
Annals of Occupational and Environmental Medicine 2019;31(1):e30-
BACKGROUND: We aimed to find the exposure level of environmental harmful substances related to the secondhand smoke (SHS) using a nationally representative data of the general population in Korea. METHODS: Total 3,533 people were included in this study. We compared the proportion exceeding 95 percentile of the concentrations of harmful substances by sex according to SHS exposure. 16 kinds of substances related to tobacco smoke were analyzed including heavy metals, polycyclic aromatic hydrocarbons, volatile organic compounds, and environmental phenol. For 16 kinds of substances, the odds ratios (ORs) for exceeding 95 percentile of each harmful substance were calculated by multiple logistic regression according to SHS exposure. Age, education level, marital status, body mass index, drinking, and exercise were adjusted as covariates. Cotinine level was additionally adjusted to increase reliability of our results. RESULTS: SHS was associated with high exposure of mercury, methylhippuric acid, fluorene, and cotinine. In women, SHS was associated with mercury, methylhippuric acid, fluorene, and cotinine, while in men, it was associated with cotinine. After adjusting covariates, ORs of blood mercury, methylhippuric acid and hydroxyfluorene in the exposed gruop were greater than that in the non-exposed group. Especially in female, methylhippuric acid and hydroxyfluorene showed consistent result. CONCLUSIONS: Our finding demonstrates that SHS is related to several harmful substances. Therefore, to reduce the health effects of SHS, it is necessary to educate and publicize the risk of SHS. Future studies are necessary to more accurately analyze factors such as exposure frequency, time, and pathway of SHS.
Adult
;
Body Mass Index
;
Cotinine
;
Cross-Sectional Studies
;
Drinking
;
Education
;
Environmental Health
;
Female
;
Humans
;
Korea
;
Logistic Models
;
Male
;
Marital Status
;
Metals, Heavy
;
Odds Ratio
;
Phenol
;
Polycyclic Hydrocarbons, Aromatic
;
Smoke
;
Tobacco
;
Tobacco Smoke Pollution
;
Volatile Organic Compounds
4.Evaluation of neuroactive effects of ethanol extract of Schisandra chinensis, Schisandrin, and Schisandrin B and determination of underlying mechanisms by zebrafish behavioral profiling.
Jia-Wei WANG ; Feng-Yin LIANG ; Xiang-Shuo OUYANG ; Pei-Bo LI ; Zhong PEI ; Wei-Wei SU
Chinese Journal of Natural Medicines (English Ed.) 2018;16(12):916-925
Schisandra chinensis, a traditional Chinese medicine (TCM), has been used to treat sleep disorders. Zebrafish sleep/wake behavioral profiling provides a high-throughput platform to screen chemicals, but has never been used to study extracts and components from TCM. In the present study, the ethanol extract of Schisandra chinensis and its two main lignin components, schisandrin and schisandrin B, were studied in zebrafish. We found that the ethanol extract had bidirectional improvement in rest and activity in zebrafish. Schisandrin and schisandrin B were both sedative and active components. We predicted that schisandrin was related to serotonin pathway and the enthanol extract of Schisandra chinensis was related to seoronin and domapine pathways using a database of zebrafish behaviors. These predictions were confirmed in experiments using Caenorhabditis elegans. In conclusion, zebrafish behavior profiling could be used as a high-throughput platform to screen neuroactive effects and predict molecular pathways of extracts and components from TCM.
Animals
;
Behavior, Animal
;
drug effects
;
Caenorhabditis elegans
;
Central Nervous System Agents
;
chemistry
;
isolation & purification
;
pharmacology
;
Cyclooctanes
;
analysis
;
isolation & purification
;
pharmacology
;
Drugs, Chinese Herbal
;
chemistry
;
pharmacology
;
Lignans
;
analysis
;
isolation & purification
;
pharmacology
;
Plant Extracts
;
chemistry
;
isolation & purification
;
pharmacology
;
Polycyclic Compounds
;
analysis
;
isolation & purification
;
pharmacology
;
Schisandra
;
chemistry
;
Zebrafish
;
physiology
5.Determination of five components in rongxin pills by HPLC.
Zhong-Ying CHU ; Li-Hong WU ; Lan TIAN
China Journal of Chinese Materia Medica 2014;39(6):1016-1019
To establish a method for determination contents of schizandrin, tanshinone I, cryptotanshinone, tanshinone II (A) and schizandrin B in rongxin pills. The HPLC method was performed on an Agilent C18. The mobile phase was composed of methnol and water wish gradient elution. The flow rate was 1.0 mL x min(-1). The column temperature was 30 degrees C and the detection wavelength wash 240 nm. The linear of schizandrin, tanshinone I, cryptotanshinone, Tanshinone II (A) and schizandrin B were 3.000-48.00 (r = 1.000), 3.985-63.76 (r = 0.999 9), 6.370-101.9 (r = 1.000), 8.690-139.0 (r = 0.999 9), 1.700-27.20 mg x L(-1) (r = 0.999 9), respectively. The average recoveries were 98.44%, 100.3%, 99.29%, 99.07%, 98.42%, and RSDs were 0.61%, 1.1%, 0.52%, 0.72%, 0.97%. The method is convenient, accurate and has good precision. It can be used for determination of the preparation.
Chromatography, High Pressure Liquid
;
Cyclooctanes
;
analysis
;
Diterpenes, Abietane
;
analysis
;
Drugs, Chinese Herbal
;
chemistry
;
Lignans
;
analysis
;
Linear Models
;
Organic Chemicals
;
analysis
;
Phenanthrenes
;
analysis
;
Polycyclic Compounds
;
analysis
;
Quality Control
;
Reproducibility of Results
6.High performance preparation and structural confirmation of lignans from Schisandrae chinensis fructus by using HSCCC combined with ESI-MSn method.
Xiao-Li YU ; Zi-feng PI ; Xiu-Li HU ; Feng-Rui SONG ; Zhi-Qiang LIU
Acta Pharmaceutica Sinica 2014;49(1):78-82
High-speed counter-current chromatography (HSCCC) was used to high performance separate and prepare lignans from Schisandrae chinensis fructus. The solvent system is composed of n-hexane-ethyl acetate-methanol-water (9 : 1 : 5 : 5) and n-hexane-ethyl acetate-methanol-water (9 : 1 : 9 : 5), speed is at 900 r.min-1, and flow rate is at 2.0 mL.min-1. Five fractions from Schisandrae chinensis fructus extract were separated and prepared with one HSCCC process. They were identified as schisandrin, gomisin J, schisandrol B, schisantherin A and deoxyschizandrin by electrospray ionization-multiple tandem mass spectrometry (ESI-MSn), respectively. Their contents were obtained in 98.74%, 94.32%, 99.53%, 94.23% and 98.68% by ultra high performance liquid chromatography (UPLC), separately. The rapid and simple method can be applied for the preparation of lignans from Schisandrae chinensis fructus.
Countercurrent Distribution
;
Cyclooctanes
;
chemistry
;
isolation & purification
;
Dioxoles
;
chemistry
;
isolation & purification
;
Drugs, Chinese Herbal
;
chemistry
;
isolation & purification
;
Fruit
;
chemistry
;
Lignans
;
chemistry
;
isolation & purification
;
Molecular Structure
;
Plants, Medicinal
;
chemistry
;
Polycyclic Compounds
;
chemistry
;
isolation & purification
;
Schisandra
;
chemistry
;
Spectrometry, Mass, Electrospray Ionization
;
Tandem Mass Spectrometry
7.Network analysis of ethanol precipitation process for Schisandrae chinensis fructus.
Yi ZHONG ; Jie-Qiang ZHU ; Xiao-Hui FAN ; Li-Yuan KANG ; Zheng LI
China Journal of Chinese Materia Medica 2014;39(17):3287-3290
A set of central composite design experiments were designed by using four factors which were ethanol amount, ethanol concentration, refrigeration temperature and refrigeration time. The relation between these factors with the target variables of the retention rate of schizandrol A, the soluble solids content, the removal rate of fructose and the removal rate of glucose were analyzed with Bayesian networks, and ethanol amount and ethanol concentration were found as the critical process parameters. Then a network model was built with 2 inputs and 4 outputs using back propagation artificial neural networks which was optimized by genetic algorithms. The R2 and MSE from the training set were 0.983 8 and 0.001 1. The R2 and MSE from the test set were 0.975 9 and 0.001 8. The results showed that network analysis method could be used for modeling of Schisandrae Chinensis Fructus ethanol precipitation process and identify critical operating parameters.
Bayes Theorem
;
Chemical Precipitation
;
Cold Temperature
;
Cyclooctanes
;
chemistry
;
Ethanol
;
chemistry
;
Fructose
;
analysis
;
Fruit
;
chemistry
;
Glucose
;
analysis
;
Lignans
;
chemistry
;
Neural Networks (Computer)
;
Polycyclic Compounds
;
chemistry
;
Reproducibility of Results
;
Schisandra
;
chemistry
;
Time Factors
8.Effect of forchlorfenuron on fruit morphology and lignans content of Schisandra chinensis.
Xin SONG ; Pu DING ; Xian-Kuan LI ; Ting CHEN ; Liang CHEN ; Bing WANG
China Journal of Chinese Materia Medica 2014;39(9):1579-1583
The effect of plant growth regulator forchlorfenuron (CPPU) 1 x 10(-6), 0.67 x 10(-6), 0.5 x 10(-6) on fruit morphology and effective components lignans was studied. Those morphologies were the combination of four basic morphological changes. The result showed, diametre were increased and longitudinal diametre of fruits were inhibited by foliage fertilizers including CPPU. At the same time, 1 000-grain weight and yield showed the varying degrees increase under CPPU. The order of the degree was 0.5 x 10(-6) > 1 x 10(-6) > 0.67 x 10(-6). Six lignans content of Schisandra chinensis of different harvest time and different CPPU processing groups were determined, the results showed that lignans accumulation occurred mainly in periods of premature the half mature fruiting stages. Under the 0.67 x 10(-6) CPPU treatment, schisandrol B, schisandrin B, schisandrin C content of S. chinensis showed different increase.
Chromatography, High Pressure Liquid
;
Cyclooctanes
;
analysis
;
metabolism
;
Dioxoles
;
analysis
;
metabolism
;
Dose-Response Relationship, Drug
;
Fruit
;
drug effects
;
growth & development
;
metabolism
;
Lignans
;
analysis
;
metabolism
;
Phenylurea Compounds
;
pharmacology
;
Polycyclic Compounds
;
analysis
;
metabolism
;
Pyridines
;
pharmacology
9.Prevention against and treatment of doxorubicin-induced acute cardiotoxicity by dexrazoxane and schisandrin B.
Kai-Yong HU ; Yong YANG ; Li-Hua HE ; Duo-Wei WANG ; Zhi-Rong JIA ; Shu-Ran LI ; Wei TIAN ; Jie MAO ; Xian-Jing LI ; Wei ZHANG
Acta Pharmaceutica Sinica 2014;49(7):1007-1012
In this study, it is to compare the effectiveness of prevention against and treatment of doxorubicin (DOX) induced cardiotoxicity by dexrazoxane and schisandrin B (Sch B) in rats. Sprague-Dawley (SD) rats were randomly divided into the following 6 groups: normal saline group, DOX group, DOX+DEX group, DOX+Sch B (80 mg x kg(-1)) group, DOX+Sch B (40 mg x kg(-1)) group and DOX+Sch B (20 mg x kg(-1)) group. The results showed that Sch B could combat the increase of myocardial enzymes in peripheral blood, decrease of the enzyme activity of myocardial tissue antioxidant enzymes and disorders of systolic and diastolic function of heart in rats intravenously injected with doxorubicin (15 mg x kg(-1)). Sch B was better than DEX in protecting rat against DOX-induced the symptoms. Sch B could protect rat against DOX-induced acute cardiomyopathy and has clinical potential applications.
Animals
;
Antibiotics, Antineoplastic
;
adverse effects
;
Antioxidants
;
metabolism
;
Cardiomyopathies
;
chemically induced
;
drug therapy
;
Cardiotoxicity
;
drug therapy
;
Cyclooctanes
;
therapeutic use
;
Dexrazoxane
;
therapeutic use
;
Doxorubicin
;
adverse effects
;
Heart
;
physiopathology
;
Lignans
;
therapeutic use
;
Myocardium
;
enzymology
;
Polycyclic Compounds
;
therapeutic use
;
Rats
;
Rats, Sprague-Dawley
10.Chemical composition, antimicrobial, insecticidal, phytotoxic and antioxidant activities of Mediterranean Pinus brutia and Pinus pinea resin essential oils.
Zeynep ULUKANLI ; Salih KARABÖRKLÜ ; Fuat BOZOK ; Burhan ATES ; Selim ERDOGAN ; Menderes CENET ; Merve Göksin KARAASLAN
Chinese Journal of Natural Medicines (English Ed.) 2014;12(12):901-910
Essential oils of the resins of Pinus brutia and Pinus pinea were evaluated for their biological potential. Essential oils were characterized using GC-MS and GC/FID. in vitro antimicrobial, phytotoxic, antioxidant, and insecticidal activities were carried out using the direct contact and the fumigant assays, respectively. The chemical profile of the essential oils of the resins of P. pinea and P. brutia included mainly α-pinene (21.39% and 25.40%), β-pinene (9.68% and 9.69%), and caryophyllene (9.12% and 4.81%). The essential oils of P. pinea and P. brutia exerted notable antimicrobial activities on Micrococcus luteus and Bacillus subtilis, insecticidal activities on Ephestia kuehniella eggs, phytotoxic activities on Lactuca sativa, Lepidium sativum, and Portulaca oleracea, as well as antioxidant potential. Indications of the biological activities of the essential oils suggest their use in the formulation of ecofriendly and biocompatible pharmaceuticals.
Animals
;
Anti-Infective Agents
;
analysis
;
pharmacology
;
Antioxidants
;
analysis
;
pharmacology
;
Bacillus subtilis
;
drug effects
;
Bicyclic Monoterpenes
;
Bridged Bicyclo Compounds
;
analysis
;
pharmacology
;
Gas Chromatography-Mass Spectrometry
;
Insecta
;
drug effects
;
Insecticides
;
analysis
;
pharmacology
;
Lepidium
;
drug effects
;
Lettuce
;
drug effects
;
Mediterranean Region
;
Micrococcus luteus
;
drug effects
;
Monoterpenes
;
analysis
;
pharmacology
;
Oils, Volatile
;
chemistry
;
pharmacology
;
Pinus
;
chemistry
;
Plant Extracts
;
chemistry
;
pharmacology
;
Plant Oils
;
chemistry
;
pharmacology
;
Polycyclic Sesquiterpenes
;
Portulaca
;
drug effects
;
Resins, Plant
;
chemistry
;
Sesquiterpenes
;
analysis
;
pharmacology
;
Terpenes
;
analysis
;
pharmacology

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