1.Clinical analysis of primary percutaneous coronary intervention in patients with acute myocardial infarction
Guo-Zhong YU ; Qing-Lian LU ; Yan-Sheng GE ; Ji-Han CHEN ; Hong-Xi CHEN ;
Chinese Journal of Primary Medicine and Pharmacy 2006;0(08):-
Objective To report the clinical effect of primary percutaneous coronary intervention(PCI)in patients with acute myocardial infarction(AMI).Methods A retrospective study was accomplished on the clinical data of 13 AMI patients who underwent PCI from March 2004 to April 2006.Results The infarct-related artery (IRA)was successfully recanalized by primary PCI for 12 AMI patients,without major complications occurred in these cases during hospitalization.Conclusion Primary PCI should be firstly chosen for treatment of AMI in the hospitals which could carry out PCI.
2.Cerebral Small Vessel Disease
Hua LI ; Ge-Lin XU ; Wen-Xin ZHAO ; Guo-Qing ZHOU ;
International Journal of Cerebrovascular Diseases 2006;0(11):-
Small vessel disease (SVD) of the cerebral white and central grey matter is an important subtype of vascular dementia (VD).SVD-dementia is characterized by a dysexecutive type of cognitive impairment,neurological deficits including imbalance and voiding dysfunction,and emotional disturbances.SVD is also frequent among clinically healthy subjects and patients with mild cognitive impairment.It is easily visualized by imaging techniques,but difficult to distinguish from mixed SVD/ Alzheimer Disease.This article reviews the recent progress in research on SVD and the problems have to be resolved.
4.Clinical analysis on 175 cases of occupational brucellosis.
Yi-wen JIANG ; Qing WANG ; Ruo-xin ZHAO ; Shu-ke GE ; Xin-wei GUO
Chinese Journal of Industrial Hygiene and Occupational Diseases 2013;31(11):861-863
Adult
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Aged
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Brucellosis
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diagnosis
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therapy
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Female
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Humans
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Male
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Middle Aged
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Occupational Diseases
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diagnosis
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microbiology
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therapy
5.Multi-sfice CT pulmonary function evaluation in emphysema
Xiao-Jun GE ; Guo-Zhen ZHANG ; Yan-Ping ZHU ; Lin SHAN ; Ding-Biao MAO ; Qi-Yong DING ; Yan-Qing HUA ;
Chinese Journal of Radiology 2001;0(03):-
Objective To explore the feasibility of evaluating the lung function by MSCT in emphysema.Methods The MSCT scan and pulmonary function tests(PFF)were respectively performed in 147 receptors within one week.They were randomly divided into 2 groups:group A(120 receptors), including normal,mild,moderate and severe abnormal pulmonary function based on the PFT,for comparing the correlation between pulmonary quantitative indexes of MSCT pulmonary function and PFT and settingup the primary grade criteria of abnormal pulmonary function in emphysema,group B(27 receptors)for evaluating the diagnostic accuracy in group A.The total lung was respectively scanned at the full inspiration and full expiration with MSCT.The pulmonary quantitative indexes of MSCT were measured with Siemens Pulmo pulmonary quantitative software.Results There was correlation between pulmonary quantitative indexes of MSCT and PFF.The Piex/in_(-910)showed best correlation with FEV_1%(r=-0.905,P
6.Controlled release by novel lysostaphin-loaded hydroxyapatite/chitosan composites.
Jin-Cheng WANG ; Bai XUE ; Kui-Kui GE ; Yi-Han WANG ; Guo-Dong LI ; Qing-Shan HUANG
Acta Pharmaceutica Sinica 2014;49(9):1331-1339
Lysostaphin is highly effective on eliminating methicillin resistant Staphylococcus aureus (MRSA). In order to achieve controlled release of lysostaphin, a biocompatible drug carrier is needed. Hydroxyapatite/chitosan (HA/CS) composites were chosen to carry lysostaphin and sample composites with different weight ratios of HA to CS, including 80/20, 70/30, 60/40, and 40/60, were prepared. Multiple analyses were performed to determine the structural and physicochemical properties of the composites, including scanning electron microscopy, X-ray diffraction and Fourier transform infrared spectroscopy. We immersed HA/CS composites loaded with 1 wt% lysostaphin to test in vitro release activity and cultured MC3T3-E1 cells to carry out biocompatibility test. The result of the release behavior of the composites revealed that the controlled release of lysostaphin from 60/40 HA/CS composites was the highest release rate of (87.4 ± 2.8)%, which lasted for 120 hours. In biocompatibility testing, MC3T3-E1 cells were able to proliferate on the surface of these composites, and the extract liquid from the composites could increase the growth of the cells. These results demonstrate the controlled release of lysostaphin from HA/CS composites and their biocompatibility, suggesting the potential application of these composites to bone injury and infection applications.
3T3 Cells
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Animals
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Biocompatible Materials
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Chitosan
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chemistry
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Delayed-Action Preparations
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Drug Carriers
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chemistry
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Durapatite
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chemistry
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Lysostaphin
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pharmacology
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Materials Testing
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Methicillin-Resistant Staphylococcus aureus
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Mice
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Microscopy, Electron, Scanning
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X-Ray Diffraction
7.Cloning of the major antigen region of E2 gene of hog cholera virus and expression in Escherichia coli.
Yong-Guo ZHANG ; Xiang-Tao LIU ; Xue-Qing HAN ; Xi-Cheng LIU ; Yan-Ming ZHANG ; Qing-Ge XIE
Chinese Journal of Biotechnology 2002;18(5):605-608
The major antigen region of E2 gene of Hog Cholera Prevalent Strain (Guangxi Yuling Strain) and Chinese Hog Cholera Lapinised Virus (C-strain) derived from hog and rabbit spleen tissue, was amplified by reverse transcription polymerase chain reaction(RT-PCR) and the nested Polymerase Chain Reaction (nPCR). After the amplified fragments were cloned into the expression vector pPROEX-HTb, the recombinant plasmids pPROEX-GXYL and pPROEX-C were obtained. The insert position, the size and the reading frame were right by PCR, restriction digestion and the sequence analysis. SDS-PAGE indicated that both of the reciepient germs transducted and induced by the recombinant plasmids pPROEX-GXYL and pPROEX-C could express the major antigen region of E2 gene. Western-blot indicated that the expressed antigen protein could be recognized by the positive serum of CSFV.
Blotting, Western
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Cloning, Molecular
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Escherichia coli
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genetics
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Polymerase Chain Reaction
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Recombinant Proteins
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biosynthesis
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Viral Envelope Proteins
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biosynthesis
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genetics
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immunology
8.Emodin inhibits dietary induced atherosclerosis by antioxidation and regulation of the sphingomyelin pathway in rabbits.
Zi-qing HEI ; He-qing HUANG ; Hong-mei TAN ; Pei-qing LIU ; Ling-zhi ZHAO ; Shao-rui CHEN ; Wen-ge HUANG ; Feng-ying CHEN ; Fen-fen GUO
Chinese Medical Journal 2006;119(10):868-870
Animals
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Antioxidants
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pharmacology
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Apoptosis
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drug effects
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Atherosclerosis
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prevention & control
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Ceramides
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analysis
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Dietary Fats
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administration & dosage
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Emodin
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pharmacology
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Lipids
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blood
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Male
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Rabbits
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Signal Transduction
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Sphingomyelin Phosphodiesterase
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metabolism
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Sphingomyelins
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metabolism
9.Prediction of Secondary Structure and B Cell Epitope for Capsid Protein of SVDV
Shi-Qi SUN ; Xiang-Tao LIU ; Hui-Chen GUO ; Shuang-Hui YIN ; Zai-Xin LIU ; Jun-Wu MA ; Qing-Ge XIE ;
China Biotechnology 2006;0(05):-
The secondary structure of Capsid protein was predicted by the methods of Chou-Fasman,Garnier-Robson and Karplus-Schultz based on the sepuence of capsid protein gene of Swine Vesicular Disease Virus (SVDV) and hydrophilicity. Surface probility plot and antigenic index for capsid protein were obtained by the methods of Kyte-Doolittle, Emini and Jameson-wolf, respectively, Combining the results according to these methods, the B cell epitopes for capsid protein of SVDV were predicted. The results showed that there are much flexible region such as coil region and turn region in capsid protein of SVDV, there are more predominant B cell epitopes in VP1 than in VP2 and VP3. This study would be helpful for identification of B cell epitopes for capsid protein using experimental methods and research of reverse vaccine of SVDV.
10.Molecular Characteristics of cDNA Encoding Bactrian Camel ?6 Subunit for FMDV Receptor
Jun-Zheng DU ; Hui-Yun CHANG ; Shan-Dian GAO ; Jing-Feng WANG ; Jun-Jun SHAO ; Guo-Zheng CONG ; Tong LIN ; Xue-Peng CAI ; Qing-Ge XIE
China Biotechnology 2006;0(08):-
Receptors play a crucial role in determining the host specificity and tissue tropism of virus. Foot-and-mouth disease virus(FMDV)has been showed to use four integrins, ?v?1, ?v?3, ?v?6 and ?v?8 as receptors to initiate infection and ?v?6 functions as the major receptor.The cDNA encoding bactrian camel integrin ?6 from the lung tissue was cloned and sequenced. The 2367bp cDNA of bactrian camel integrin ?6 encodes a polypeptide of 788 amino acids consisting of a 26-residue putative signal peptide, a 681-residue ectodomain with 8 potential N-linked glycosylation sites and 58 cysteine residues, a 29-residue transmembrane domain, and a 52-residue cytoplasmic domain with a NPLY motif and 1 potential N-linked glycosylation site. The nucleotide sequence similarity of integrin ?6 between bactrian camel and cattle, pig, sheep, human, mouse, Norway rat is 91.1%、91.8%、90.6%、90.5%、83.7%、84.1%, and the amino acid sequence similarity is 94.3%、93.4%、93.4%、93.7%、88.7%、88.6%, respectively. The bactrian camel ?6 gene exhibited the higher sequence homology with the ?6 gene of cattle, pig and sheep, indicating their close genetic relationships. It is possible that host tropism of FMDV may related to divergence in ?6 receptors among different species.