1.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
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Cyclooctanes
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analysis
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metabolism
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Dioxoles
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analysis
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metabolism
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Dose-Response Relationship, Drug
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Fruit
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drug effects
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growth & development
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metabolism
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Lignans
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analysis
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metabolism
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Phenylurea Compounds
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pharmacology
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Polycyclic Compounds
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analysis
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metabolism
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Pyridines
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pharmacology
2.Identification of Schisandra chinensis with white fruits based on ITS2 sequences.
Xian-Kuan LI ; Bing WANG ; Yan-Chao ZHENG ; Cong LIU ; Pu DING ; Xin SONG
China Journal of Chinese Materia Medica 2014;39(11):2011-2015
OBJECTIVETo analyse a special kind of Schisandra chinensis with the white fruit using ITS2 barcode at molecular levels.
METHODITS2 regions were sequenced bidirectionally. Sequence assembly and consensus sequence generation were performed using the CodonCode Aligner, MEGA 5.0 software was used to align the sequences. The ITS2 secondary structure was predicted using ITS2 web server, BLAST 1 method was used to identify the S. chinensis with the white fruit.
RESULTThe length of the ITS2 sequence was 231 bp. And the sample was identified as S. chinensis using the method of BLAST 1. Their mean interspecific genetic distance (K2P distance) among the populations of the S. chinensis with the white fruit and S. chinensis was far lower than the mean interspecific genetic distance between the S. chinensis and S. sphenanthera.
CONCLUSIONBy using ITS2 the S. chinensis with the white fruit was identified as S. chinensis, and the ITS2 barcode could be used to identify S. chinensis and S. sphenanthera.
DNA, Plant ; chemistry ; genetics ; DNA, Ribosomal Spacer ; chemistry ; genetics ; Fruit ; chemistry ; classification ; genetics ; Molecular Sequence Data ; Nucleic Acid Conformation ; Schisandra ; chemistry ; classification ; genetics ; Sequence Analysis, DNA ; Software
3.Clinical efficacy and safety analysis of ibutilide and propafenone in the treatment of patients with atrial fibrillation
Dong WANG ; Kuan WANG ; Xin-Ping DU
The Chinese Journal of Clinical Pharmacology 2015;(15):1475-1476,1493
Objective To evaluate the clinical efficacy and safety of ibutilide and propafenone in the treatment of patients with atrial fibrilla-tion.Methods A total of 66 patients with atrial fibrillation were included in this study.Of the recruited 66 subjects, 31 cases ( experiment group ) received ibutilide 1 mg by intravenous injection within 10 min and other 35 cases ( control group) received propafenone 70 mg by intravenous injection within 10 min.The treatment procedure were done again if the atrial fibrillation still existed after administration.The successful rate and adverse reactions were recorded in the two groups.Results The successful rate was 74.2% in experiment group and 51.4%in control group with statistical difference ( P<0.05 ).The median time of cardioversion was 20.5 min for experiment group and 25.2 min in control group with significant difference ( P<0.05 ).The rate of adverse reactions were 29.0% and 25.7% in the treatment and control group, respectively without statistical difference ( P >0.05 ).Conclusion The successful rate of ibutilide in the treatment of patients with atrial fibrillation is relative higher with short period of time for success.
4.Forensic application of 30 InDel loci in Han and She nationalities of Eastern China.
Zhen HU ; Zheng WANG ; Su-hua ZHANG ; Shu-min ZHAO ; Ru-xin ZHU ; Kuan SUN ; Cheng-tao LI
Journal of Forensic Medicine 2014;30(5):337-345
OBJECTIVE:
To evaluate the forensic application value of 30 insertion/deletion (InDel) loci included in Investigator DIPplex Kit in Han and She nationalities of Eastern China.
METHODS:
A total of 565 unrelated individuals in Han nationality and 119 ones in She nationality of Eastern China were investigated using Investigator DIPplex Kit. Allele frequencies, population genetics parameters of the 30 InDel loci were statistically calculated.
RESULTS:
In Han nationality, the mean Ho was 0.413 3, the mean DP was 0.551 1, the mean PIC was 0.320 0. And in She nationality, the mean Ho was 0.389 6, the mean DP was 0.543 3, the mean PIC was 0.310 0. No deviation from Hardy-Weinberg equilibrium was observed in Han and She nationalities (P > 0.05).
CONCLUSION
The 30 loci in Investigator DIPplex Kit show good genetic diversity in Han and She nationalities, and could be used as a supplemental tool for some special paternity cases.
Asian People/genetics*
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China
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Ethnicity/genetics*
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Female
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Forensic Genetics
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Gene Frequency
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Genetic Variation
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Genetics, Population
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Humans
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INDEL Mutation/genetics*
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Polymorphism, Genetic
5.Diagnostic value of combined modified Alvarado scores and computed tomography imaging in the pathological types of acute appendicitis in adults.
Shi-kuan LI ; Hai-kuan WANG ; Yuan-bo LI ; Xin-gang PENG ; Pei-ge WANG ; Yan-bing ZHOU ; Xiao-bin ZHOU
Chinese Journal of Gastrointestinal Surgery 2012;15(12):1227-1231
OBJECTIVETo explore the diagnostic value of combined modified Alvarado scores (MAS) and computed tomography imaging in the pathological types of acute appendicitis in adults.
METHODSClinical data of a total of 396 adult patients with acute appendicitis confirmed by surgery and pathology were analyzed retrospectively from June 2007 to July 2010. Case-control study was used to investigate the MAS. CT signs were studied in 115 patients who underwent preoperative CT scan. Univariable analysis was performed using each indicator among different pathological types. Discriminant classification was formed by applying significant variables identified from univariable analysis and a Fisher discriminant function was created.
RESULTSTwenty three variables were statistically significant among different pathological types after univariable analysis(P<0.05) and were selected for discriminant analysis. Six variables including temperature(X1), leucocyte count(X2), the proportion of neutrophil(X3), MAS points(X4), periappendiceal fat stranding(X5), and extraluminal air(X6) were enrolled. The discriminant function equation was Y1=0.012X1+0.041X2+0.069X3-0.039X4+2.653X5+1.418X6, Y2=0.327X1+0.041X2-0.034X3-0.140X4-1.114X5+2.982X6. The accuracy was 76.5%(88/115) in retrospective assessment and 77.8%(21/27) in prospective assessment.
CONCLUSIONThe combined use of MAS and CT imaging signs is useful in identifying the pathological types of acute appendicitis in adults, so it is helpful in choosing reasonable therapeutic option for surgeons.
Acute Disease ; Appendicitis ; diagnosis ; Case-Control Studies ; Humans ; Retrospective Studies ; Sensitivity and Specificity ; Tomography, X-Ray Computed
6.Enhancement of meniscal repair in the avascular zone using connective tissue growth factor in a rabbit model.
Wei HE ; Yu-Jie LIU ; Zhi-Gang WANG ; Zi-Kuan GUO ; Ming-Xin WANG ; Ning WANG
Chinese Medical Journal 2011;124(23):3968-3975
BACKGROUNDConnective tissue growth factor (CTGF) is a secreted protein containing several domains that mediate interactions with growth factors, integrins and extracellular matrix components. CTGF plays an important role in extracellular matrix production by its ability to mediate collagen deposition during wound healing. CTGF also induces neovascularization in vitro, suggesting a role in angiogenesis in vivo. We herein evaluated whether CTGF was required for extracellular matrix synthesis of meniscal fibrochondrocytes and/or angiogenesis during the repair of meniscal tears.
METHODSMeniscal fibrochondrocytes were isolated from the inner-1/2 of rabbit meniscus by trypsin collagenase treatment and further treated with 100 ng/ml CTGF in vitro. Characterization of fibrochondrocytes was identified by flow cytometry analyzing CD31, CD44, CD45 and CD105, and was further tested by type II collagen immunocytochemistry. Changes in gene expression of meniscal fibrochondrocytes were monitored by quantitative real-time polymerase chain reaction. Histological sections prepared from a 3-mm portion of a longitudinal tearing defect in the middle of the rabbit meniscus were subjected to fluorescence-immunohistochemistry analysis at 1, 4 and 10 weeks following surgical treatment with 1.5 µg of CTGF/fibrin-glue composites.
RESULTSQuantitative RT-PCR assay showed that types I and II collagen and vascular endothelial growth factor mRNA expression in the 100 ng/ml CTGF group were remarkably enhanced as compared to levels in the no-dose group at 14 days ((2.38 ± 0.63) fold, (2.96 ± 0.87) fold, (2.14 ± 0.56) fold, respectively). Likewise, fluorescence-immunohistochemical analysis revealed that in the group implanted with CTGF-fibrin glue, types I and II collagen, as well as the capillaries, completely filled the defect by 10 weeks, postoperatively. In contrast, only soft tissue repair occurred when PBS-fibrin glue was implanted.
CONCLUSIONSThese findings suggest that CTGF can significantly promote extracellular matrix deposition (types I and II collagen) within the meniscal avascular zone; CTGF can greatly heighten the expression of vascular endothelial growth factor activity simultaneously in vivo, further enhancing the repair of meniscal tears in the avascular zone.
Animals ; Cells, Cultured ; Chondrocytes ; cytology ; Collagen Type I ; metabolism ; Collagen Type II ; metabolism ; Connective Tissue Growth Factor ; pharmacology ; Flow Cytometry ; Immunohistochemistry ; Male ; Menisci, Tibial ; cytology ; Rabbits ; Reverse Transcriptase Polymerase Chain Reaction ; Tibial Meniscus Injuries ; Vascular Endothelial Growth Factor A ; metabolism ; Wound Healing ; drug effects
7.Clinical efficacy and safety of tirofiban in the treatment of patients who received percutaneous coronary intervention
Kuan WANG ; Dong WANG ; Liu-Ying ZHENG ; Guo-Xing ZUO ; Ming-Hui ZHANG ; Xin-Ping DU
The Chinese Journal of Clinical Pharmacology 2014;(5):397-398,413
Objective To evaluate the clinical efficacy and safety of tirofiban in the treatment of patients who received percutaneous coronary intervention( PCI).Methods Eighty-seven patients with acute coro-nary syndrome treated with PCI were recruited from Feb 2011 to Sep 2013 prospectively.They were randomly divided into treatment group ( n=41 ) and control group ( n=46 ).Based on the regular anticoagulant therapy , patients in the treatment group were given tirofiban 10 mg· kg-1 immediately at the early time of pre -PCI, followed by 0.15μg· kg -1 · min -1 intravenous infusion until 36 hours after PCI.Patients in the control group were only given the regular anticoagulant therapy at the early time of pre-PCI.And the major adverse cardiovascular events (MACE), myocardial enzymes and complication of the two groups were observed in the two groups.Results The rate of MACE (9.8%, 4/41) in treatment group were much lower than that in the control group (26.1%, 12/46) ( P<0.05 ).The myocardial enzyme indicators of 24 hours after PCI was lower than that in the control group;but there was no difference in bleeding complications between the two groups ( P>0.05 ) . Conclusion MACE can be significantly decreased in patients who were treated with PCI by using tirofiban in the emergency department and tiro-fiban does not increase the risks to develop bleeding complications.
9.HPLC determination of six lignans in different parts of Schisandra chinensis.
Pu DING ; Bing WANG ; Xin SONG ; Xian-Kuan LI ; Ting CHEN ; Cong LIU
China Journal of Chinese Materia Medica 2013;38(13):2078-2081
OBJECTIVETo compare the content of six lignans of different parts of Schisandra chinensis.
METHODAgilent TC-C18 (4.6 mm x 250 mm, 5 microm) was used with acetonitrile-water gradient system as mobile phase. Wave length was 250 nm. The flow rate was 1 mL x min(-1). Column temperature was 30 degrees C.
RESULTThe total lignans content of wild Schisandra chinensis was higher than that of the cultivated varieties. The total lignans content of different parts varied significantly, wherein the root > main branch > side branches > leaf.
CONCLUSIONThis method is stable, reliable, can be used for the quality evaluation of different parts of Schisandra.
Chromatography, High Pressure Liquid ; methods ; Lignans ; analysis ; Schisandra ; chemistry
10.The expression of humanized Fab fragment of the anti-HBsAg antibody in methylotropic yeast Pichia pastoris.
Ning DENG ; Kuan-Yuan SU ; Xun-Zhang WANG ; Qing-Xin LONG ; Lin YANG ; Zhou-Yao YU
Chinese Journal of Biotechnology 2002;18(5):546-550
Using of two-step integrating technology, transducted the H and L chain gene of humanized Fab fragment of anti-HB-sAg antibody into the genome of methylotropic yeast P. pastoris. Constructed a engineering yeast to produce humanized Fab fragment of the anti-HBsAg antibody. The Fab fragment was efficiently secreted into the medium at a concentration of 50-80 mg/L. The Fab fragment was purified from culturing supernatant of the recombinant yeas by affinity chromatography. The ELISA analysis showed the high affinity of the expressed humanized Fab fragment to the HBsAg.
Chromatography, Affinity
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Cloning, Molecular
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Enzyme-Linked Immunosorbent Assay
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Hepatitis B Antibodies
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biosynthesis
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genetics
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isolation & purification
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Hepatitis B Surface Antigens
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immunology
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Humans
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Immunoglobulin Fab Fragments
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biosynthesis
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genetics
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isolation & purification
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Pichia
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genetics
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Recombinant Proteins
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biosynthesis
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isolation & purification