2.Studies on chemical constituents and volatile oil of Xiaochengqi decoction.
Miao-Xuan FAN ; Hong-Jie WANG ; Xiao-Ming LI ; Peng-Yue LI ; Bao-Lin BIAN
China Journal of Chinese Materia Medica 2008;33(9):1027-1031
OBJECTIVETo study the chemical constituents and volatile oil of Xiaochengqi decoction.
METHODThe constituents in decoction were separated by means of column chromatography and their structures were identified by spectral data and compared with literature data. As well as the volatile oil of Xiaochengqi Fang were analyzed and identified by GC-MS.
RESULTEleven compounds were isolated and identified as chrysophanol (1), physcion (2), magnolol (3), beta-sitosterol (4), sitosterol trans-cinnamic acid (5), emodin (6), aloe emodin (7), rhein (8), gallic acid (9), chrysophanol-8-O-beta-D-glucopyranoside (10), aurantiamarin (11). The volatile oils extracted with steam distillation from Xiaochengqi were identified 67 components, and the main components are including.
CONCLUSIONAll of the eleven compounds were isolated from Xiaochengqi decoction for the first time and the study on their activities in Chinese prescription is being carried out. D-limonene (42.61%), p-cymene (16.43%), and 8-terpinene (14.46%).
Anthraquinones ; chemistry ; Biphenyl Compounds ; chemistry ; Cinnamates ; chemistry ; Cyclohexenes ; chemistry ; Drugs, Chinese Herbal ; chemistry ; Emodin ; analogs & derivatives ; chemistry ; Gallic Acid ; chemistry ; Gas Chromatography-Mass Spectrometry ; Lignans ; chemistry ; Monoterpenes ; chemistry ; Oils, Volatile ; chemistry ; Sitosterols ; chemistry ; Terpenes ; chemistry
3.Effects of CNTF on the nuclear translocation of PKC following NMDA administration in primary hippocampal neurons.
Fang LIU ; Jin YAN ; Zong-lai JIANG ; Xue-qi WANG ; Xuan BAO ; Chang-lin LU
Chinese Journal of Applied Physiology 2003;19(2):145-148
AIMTo investigate the effect of ciliary neurotrophic factor (CNTF) on the nuclear translocation of protein kinase C (PKC) following NMDA administration in the primary cultured hippocampal neurons.
METHODS(1) PKCGAMMA or PKCepsilon- immunocytochemistry staining method was used after treating neurons with NMDA or CNTF. (2) The gray of the nucleus of the PKC-positive neurons were measured under the image pattern analysis system.
RESULTS(1) After NMDA administration of different concentration and time, Nucleus appear PKCgamma and PKCepsilon activities, especially the 100 micromol/L NMDA 30 min group. (2) The gray of nucleus in CNTF + 500 micromol/L NMDA group is similar to control group.
CONCLUSIONNMDA can induce nuclear translocation of PKC in the primary cultured hippocampal neurons, and CNTF can inhibit the translocation. It suggests that the inhibition of PKC translocation induced by NMDA is one of the important reasons for the neuro-protective effects of CNTF.
Animals ; Cells, Cultured ; Ciliary Neurotrophic Factor ; pharmacology ; Hippocampus ; cytology ; N-Methylaspartate ; pharmacology ; Neurons ; drug effects ; metabolism ; Protein Kinase C ; metabolism ; Protein Transport ; Rats ; Rats, Sprague-Dawley
4.Comparison of three methods in construction fusion gene of influenza A virus Nucleoprotein
Bo LIU ; Bao-Lin WANG ; Ling CHEN ; Jing YAN ; Jian-Yong ZHANG ; Hong-Xuan HE ; Hong ZHANG
Chinese Journal of Experimental and Clinical Virology 2012;26(1):70-74
Objective To develop a best method of constructing influenza NP fusion gene containing enhanced green fluorescent protein (EGFP).Methods The full-length NP gene of influenza A was amplified by RT-PCR and was inserted into an eukaryotic expression vector pEGFP-N1 in order to construct a fusion gene of pEGFP-N1-NP using three different methods.Method one,NP gene containing restriction endonucleases and pEGFP-N1 were both digested using the same restrict enzymes and ligated,yielding the fusion gene of pEGFP-N1-NP. Method two,NP gene was cloned into pMD19-T Vector to construct a plasmid of pMD19-T-NP.The pMD19-T-NP cloned into pEGFP-N1 to construct the fusion gene of pEGFP-N1-NP; Method three,NP gene containing restriction endonucleases was cloned into pMD19-T Simple Vector to construct a plasmid of pMD19-T-NP.The pMD19-T-NP cloned into pEGFP-N1 to construct the fusion gene of pEGFP-N1-NP.Results The fusion gene of recombinant eukaryotic expression vector pEGFP-N1-NP was successfully constructed by using method three.Conclusions The full-length NP gene is obtained and its fusion gene of recombinant eukaryotic expression plasmid is successfully constructed.This study provides foundation for further understanding the biological function of NP protein and the mechanism of diseases induced by influenza A virus.
5.Qualitative analysis of batch preparing cryopreserved fresh platelet rich plasma.
Xi-Lin OUYANG ; Jing-Han LIU ; Ji-Chun PAN ; Xi-Jin LI ; Shu-Xuan MA ; Hai-Bao WANG ; Feng-Lei LAI ; Da-Yong GAO
Journal of Experimental Hematology 2004;12(6):841-844
To evaluate the efficiency and effectiveness of batch preparing cryopreserved fresh platelet-rich plasma (cryo-FPRP) derived from the volunteer donors, platelet count (Plt), mean platelet volume (MPV), platelet distribution width (PDW), plasma pH, plasma lactic acid concentration, and lactic dehydrogenase (LDH) concentration, germiculture, CD62p positive rate, PAC-1 positive rate, and the fluorescence intensity of platelet GPIb-IX-V were detected in ACD whole blood, fresh platelet-rich plasma (FPRP), FPRP with 5% dimethyl sulphoxide DMSO (DMSO-FPRP), and thawed cryopreserved FPRP (cryo-FPRP); the procoagulant activity of FPRP and cryo-FPR was determinated. The results showed that (1) 70 percentage of platelet were separated from the whole blood into FPRP, and the counts of residual erythrocyte and leucocyte were below 1 x 10(9), and below 1 x 10(7) per unit respectively. (2) The plasma pH, lactic acid concentration and PAC-1 positive rate retained a stable level during the preparing, storing and thawing process. (3) Plasma LDH concentration, platelet CD62p positive rate and GPIb-IX-V concentration in platelet surface were enhanced significantly after being frozen and thawing. (4) The plasma clotting time induced by cryo-FPRP were significantly shorter than that induced by FPRP. It is concluded that: (1) The batch platelet preparing process can efficiently obtain platelet from whole blood donated by volunteer, and the process didn't activate the platelet. (2) Cryopreservation can prevent lactic acid accumulation, pH reduce and activation of GPIIb/IIIa. (3) The membrane of partial platelets are affected by freezing and thawing. (4) The density of GPIb-IX-V complexes in platelet surface and its procoagulant activity are enhanced significantly after the FPRP freezing and thawing process.
Blood Platelets
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cytology
;
metabolism
;
Blood Preservation
;
methods
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Cryopreservation
;
methods
;
E-Selectin
;
blood
;
Humans
;
Hydrogen-Ion Concentration
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L-Lactate Dehydrogenase
;
blood
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Lactic Acid
;
blood
;
Platelet-Rich Plasma
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metabolism
;
Reproducibility of Results
6.Determination and comparison of anti-SARS antibody in children and adults.
Jing-Han LIU ; Shu-Xuan MA ; Xi-Lin OUYANG ; Hai-Bao WANG ; Yang YU ; Xi-Jin LI ; Ting ZHANG ; Suo-Qin TANG
Journal of Experimental Hematology 2004;12(2):217-219
To investigate the positive rate of anti-SARS antibody in children and adults without SARS, 197 paediatric patients under 14 years old from inpatient and outpatient department of our hospital, 156 healthy children pupils from primary school, 453 adult patients over 18 years old from inpatient and outpatient department of our hospital and other 502 healthy adult blood donors were selected. Anti-SARS antibodies were determined by anti-SARS specific antibody detection kit and ELISA method. The results showed that both the positive rates of IgG antibody in paediatric patients and healthy children were about 2% (4/197 and 3/156), while the positive rates in adult patients and healthy adults were about 0.2% (1/453 and 1/502). The difference between the positive rates of children and adults was significant (chi(2) = 11.61, P < 0.001). IgM antibody was negative in all the samples. It is concluded that the anti-SARS IgG antibody positive rate in children was obvious higher than that in adults. This may be the cause why the cases with SARS in children is much less than in adults.
Adult
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Age Factors
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Aged
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Antibodies, Viral
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blood
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Child
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Child, Preschool
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Female
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Humans
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Immunoglobulin G
;
blood
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Male
;
Middle Aged
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SARS Virus
;
immunology
7.Prenatal diagnosis of achondroplasia.
Xuan HUANG ; Lin-huan HUANG ; Qun FANG ; Min-ling CHEN ; Yi ZHOU ; Jian CAI ; Bao-jiang CHEN ; Jun-hong CHEN
Chinese Journal of Medical Genetics 2008;25(4):427-429
OBJECTIVETo diagnose achondroplasia prenatally by FGFR3 gene detection.
METHODSSeventy-eight fetuses affected by short-limb dysplasias were recruited. Umbilical blood sampling was employed to obtain fetal blood for karyotyping and FGFR3 gene detection. Genomic DNA was extracted, and the exon 10 of the FGFR3 gene was amplified. PCR amplicons were analyzed by DNA sequencing and restriction fragment length polymorphism with Bfm I. The FGFR3 exon 10 from the parents of the positive fetuses was screened by the same method.
RESULTSIn 78 fetuses affected with short-limb dysplasias, 8 cases had G1138A heterozygotic mutation and normal karyotype, and were diagnosed as achondroplasia. The other 70 fetuses had normal nucleotide at nucleotide 1138 in exon 10 of FGFR3, therefore were excluded from achondroplasia. Only one father in parents of the 8 achondroplasia fetuses also had the G1138A mutation.
CONCLUSIONAchondroplasia could be diagnosed prenatally in the fetuses affected with short-limb dysplasias by using PCR-RFLP and DNA sequencing of the exon 10 of the FGFR3 gene.
Achondroplasia ; diagnosis ; genetics ; DNA Mutational Analysis ; Female ; Humans ; Male ; Polymorphism, Restriction Fragment Length ; Pregnancy ; Prenatal Diagnosis ; methods ; Receptor, Fibroblast Growth Factor, Type 3 ; genetics
8.Construction of multi-dimensional value evaluation index system of intraocular lens
Bao-Ying TAN ; Ai-Ling LIN ; Huang-Ying SUN ; Xin PENG ; Chuan-Chao LUO ; Jian-Wei XUAN
Chinese Medical Equipment Journal 2023;44(11):83-89
Objective To develop two multi-dimensional value evaluation index systems for intraocular lens(IOL)to assist decision makers in selecting appropriate IOLs.Methods IOL value assessment indexes were determined preliminarily through literature research and expert consultation,and the weights of the indexes were calculated through hierarchical analysis method and then ranked to form two evaluation index systems.Results Two multi-dimensional value evaluation index systems were constructed for monofocal and refractive IOLs respectively,which both contained 3 first-level indicators and 13 second-level indicators;the evaluation index system for monofocal IOL involved in 26 third-level indicators,and the other for refractive IOL had 33 third-level indicators.The three first-level indicators of the two systems were ranked by weight as clinical dimension,economic dimension and institutional dimension.The monofocal IOL evaluation index system had product performance being the second-level indicator with the highest weight,and the top three third-level indicators with the highest weights being lens capsule biocompatibility,risk of intraocular lens damage during implantation and range of applicable populations;the refractive IOL evaluation index system had clinical efficacy(vision)being the second-level indicator with the highest weight,and the top three third-level indicators with the highest weights being distant vision,(astigmatism)rotational stability/postoperative axial rotation and near vision.Conclusion The multi-dimensional value evaluation index systems developed provide references for comprehensive value evaluation of IOLs.[Chinese Medical Equipment Journal,2023,44(11):83-89]
9.Influences of cycle index and volume on sensitivity of DNA detection.
Lu ZHANG ; Bao-Jie WANG ; Mei DING ; Zi-Qing LIN ; Hao PANG ; Jia-Xin XING ; Jin-Feng XUAN
Journal of Forensic Medicine 2013;29(2):125-126
OBJECTIVE:
To explore the feasibility of improving the sensitivity of DNA detection by increasing the PCR cycle index and decreasing the volume of amplifying system.
METHODS:
The DNA of semen were collected from 10 healthy irrelevant volunteers, and were quantified to 50, 40, 30, 25, 20, 15, 10 pg/microL, separately. All samples were then amplified in 10, 5, 3 microL volume and at 28, 30, 32, 34, 36 cycles, respectively. 3130 genetic analyzer was used to detect 15 autosomal STR loci.
RESULTS:
Under the situation of 28 cycles and 3 microL volume, samples which achieved > 40 pg/microL could be correctly typed. Under the situation of 10, 5, 3 microL volume, samples which achieved > 20 pg/microL could be correctly typed at 34 cycles. When increasing the index to 36 cycles, they could not be correctly typed because of the non-specific band.
CONCLUSION
DNA detecting sensitivity can be improved to a certain extent by increasing the cycle index and decreasing the volume of amplifying system.
DNA/genetics*
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DNA Fingerprinting/methods*
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Feasibility Studies
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Forensic Genetics/methods*
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Humans
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Limit of Detection
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Male
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Polymerase Chain Reaction/methods*
;
Semen/chemistry*
;
Sensitivity and Specificity
;
Tandem Repeat Sequences
10.Multicenter follow-up study of ankle fracture surgery.
Hai-lin XU ; Li-min LIU ; Xuan LI ; Dian-ying ZHANG ; Zhong-guo FU ; Tian-bing WANG ; Pei-xun ZHANG ; Bao-guo JIANG ; Hui-liang SHEN ; Gang WANG ; Guang-lin WANG ; Xin-bao WU
Chinese Medical Journal 2012;125(4):574-578
BACKGROUNDFew data on ankle fractures in China from large multicenter epidemiological and clinical studies are available. The aim of this research was to evaluate the epidemiological features and surgical outcomes of ankle fractures by reviewing 235 patients who underwent ankle fracture surgery at five hospitals in China.
METHODSThis study included patients who underwent ankle fracture surgery at five Chinese hospitals from January 2000 to July 2009. Age, gender, mechanism of injury, Arbeitsgemeinschaft für Osteosynthesefragen (AO) fracture type, fracture pattern, length of hospital stay and treatment outcome were recorded. Statistical analyses were conducted using SPSS software. The American Orthopedic Foot and Ankle Society (AOFAS) ankle-hindfoot scale, visual analogue scale (VAS), and arthritis scale were used to evaluate outcome.
RESULTSOf 235 patients with ankle fractures, 105 were male with an average age of 37.8 years and 130 were female with an average age of 47.3 years. The average follow-up period was 55.7 months. There were significant differences in the ratios of patients in different age groups between males and females, and in mechanisms of injury among different age groups. There were also significant differences in the length of hospital stay among different fracture types and mechanisms of injury. In healed fractures, the average AOFAS ankle-hindfoot score was 95.5, with an excellence rate of 99.6%, the average VAS score was 0.17, and the average arthritis score was 0.18. Movement of the injured ankle was significantly different to that of the uninjured ankle. There were no significant differences between AO fracture types, fracture patterns or follow-up periods and AOFAS score, but there were some significant differences between these parameters and ankle joint movements, pain VAS score and arthritis score.
CONCLUSIONSAnkle fractures occur most commonly in middle-aged and young males aged 20 - 39 years and in elderly females aged 50 - 69 years. The most common mechanisms of injury are twisting injuries and falls from a standing height or less. The results of surgical treatment are satisfactory.
Adult ; Age Distribution ; Ankle Injuries ; surgery ; Female ; Humans ; Male ; Middle Aged ; Sex Distribution ; Treatment Outcome