2.Analysis of Polysomnagraphy in Pediatric Obstructive Sleep Apnea Hypopnea Syndrome with Different Body Mass Index
feng-feng, HAN ; jian-hai, LIN
Journal of Applied Clinical Pediatrics 2003;0(10):-
Objective To investigate the relationship of pediatric obstructive sleep apnea hypopnea syndrome (OSAHS) with different body mass mdex(BMI) and the severity of OSAHS. Methods Nine children with high BMI, 10 children with low BMI and 25 children with normal BMI which were monitored and diagnosed OSAHS by nocturnal polysonmography(PSG ) ,and the parameters of PSG were analyzed. Results The high BMI group findings were significantly higher AHI(21.61 ? 7.42 vs 11.32?4.16 P
3.Prokaryotic expression,identification,primary purification of human prostate specific membrane antigen
Hai HUANG ; Jian HUANG ; Tianxin LIN ; Al ET
Chinese Journal of Urology 2001;0(08):-
Objective To describe the cloning of cDNA of prostate specific membrane antigen (PSMA),construction of the recon of PSMA,induction of the expression of 6 ? His PSMA fusion protein from PSMS recon,and purification of the expression products. Methods The total RNA was extracted from prostate cancer tissues.The site of EcoR I lying in the middle of PSMA’s cDNA was used to perform the reverse transcriptase and polymerase chain reaction of PSMA in two different parts,which were then linked into the carrier of pEt 30(a),thus the full cDNA of PSMA and the pronucleus expression carrier pET 30(a) PSMA were obtained.The pET30a (+) PSMA recon was transformed into the Escherichia coli BL 21 and the engineering bacteria expressing protein PSMA was gotten. With the induction of IPTG, the recon was expressed. The expression products were purified with Ni NTA Agarose resin, then the purer protein PSMA was obtained. The antigenicity and specificity of the expressed PSMA were evaluated with Western blotting and SDS PAGE. Results The wholly right base sequence of PSMA’s cDNA was successfully cloned.PSMA protein was expressed and purified.This protein had better antigenicity and specificity. Conclusions This study provides experimental basis for the function study of PSMA and scanning of the phage antibody library.
5.Investigation and analysis of correlated factors on mental health of peacekeeping forces in Liberia dispatched from Pakistan and Bangladesh
Chunxia CHEN ; Wei GUO ; Jian GUO ; Hai LIN ; Liyi ZHANG
Medical Journal of Chinese People's Liberation Army 2001;0(09):-
Objective To investigate the status and influential factors of mental health of Pakistani and Bangladeshi peacekeeping forces in Liberia.Methods By random sampling,300peacekeeping officers and soldiers dispatched from Pakistan and Bangladesh(150 each)in Liberia were investigated with Chinese Military Mental Health Scale(CMMHS),Military Mental Maladjustment Scale(MMMS) and Social Support Rating Scale(SSRS),and they were carried out for two times on the 7th day and the 120th day after arrival in peacekeeping mission area.Results The total score and each factor score of CMMHS(except for obsessive-compulsive,anxiety and interpersonal sensitivity)and the total score of MMMS of the peacekeepers at the 7th day after their arrival in mission area were significantly higher than those at the 120th day(P
6.Effects of tetramethylpyrazine on fibrosis of atrial tissue and atrial fibrillation in a canine model of congestive heart failure induced by ventricular tachypacing.
Yazhou LIN ; Chunxuan XU ; Yulian DENG ; Lin CHEN ; Hai HUANG ; Jian DU
Journal of Integrative Medicine 2006;4(1):35-8
To explore the effects of tetramethylpyrazine (TMP) on fibrosis of atrial tissue and atrial fibrillation in a canine model of congestive heart failure (CHF) induced by ventricular tachypacing.
7.Expression of Recombinant Snake Venom Cystatin in Yeast Pichia pastoris and Its Effects on B16F1 Melanoma Invasion in vitro
Rong WAN ; Jun SONG ; Hai-Ying ZHENG ; Xiao-Yan ZHANG ; Xu LIN ; Jian-Yin LIN ;
China Biotechnology 2006;0(07):-
To investigate the biological role of snake venom cystatin(sv-cystatin) in tumor progression, the cDNA of sv-cystatin amplified by PCR from pUC18-cystatin plasmid was cloned into methanol-inducible expression vector pPICZ?A. The linearized recombinant plasmid pPICZ?A-cystatin was transfered into Pichia pastoris, strain GS115 by electrophoration. Transfermants with phenotype Mut+ selected were identified by PCR analysis and induced in 1.0% methanol. The reombinant sv-cystatin protein was examined by SDS-PAGE, Western blot analysis. The molecular mass of expression product was about 14 kDa and approximately 16 mg/L of recombinant sv-cystatin was produced from one of GS115-cystatin transformants. The chromatography purified protein could reduce the activity of papain. The ability of B16F1 cells treated with recombinant sv-cystatin to invade the reconstituted basement membrane decreased significantly (P
8.Culture and differentiation of bone marrow mesenchymal stem cells on bladder acellular matrix
Zuoqiang LIU ; Hai HUANG ; Jian HUANG ; Tianxin LIN ; Kewei XU ; Zhenghui GUO ; Chun JIANG ; Jinli HAN
Chinese Journal of Tissue Engineering Research 2008;12(14):2780-2784
BACKGROUND:Smooth muscle cells and transitional epithelial cells were traditionally used to construct tissue-engineered bladder and to perform double-sided implantation of scaffold.However,double-sided implantation is difficult to perform,because smooth muscle cells are difficult to isolate or culture in vitro and passage is limited.OBJECTIVE:To verify the feasibility of tissue-engineered bladder reconstruction with bone marrow mesenchymal stem cells(BMSCs)and bladder acellular matrix(BAM).DESIGN:A basic empirical study.SETTING:Linbaixin Medical Research Center,Second Affiliated Hospital,Sun Yat-sen University.MATERIALS:Experiments were performed at the Linbaixin Medical Research Center,Second Affiliated Hospital,Sun Yat-sen University from March 2006 to Mav 2007.The laboratory was the Opening Laboratory of Hospital Affiliated to Health Department of China.One-month old SD rats of either sex,weighting 80-100 g were provided by Animal Experimental Center of Sun Yat-sen University.Fresh porcine bladders were offered by Animal Experimental Center of Southern Medical University.METHODS:Whole bone marrow culture and successive adherence method was used to culture rat BMSCs in vitro.Flow cytometry was employed to detect surface antigen.Eradicator washing method was applied to prepare porcine BAM and measure its purity and characteristies.Third passage of BMSCs were inoculated in BAM and cultured in a medium containing vascular endothelial growth factor(VEGF165)(25 ng/L)in vive and in vitro to test compatibility.Cells cultured alone were considered to be controls for the in vivo trial,and materials non-implanted with cells were considered to be controls for in vitro trial.Suitable microenvironment was simulated to induce the differentiation of BMSCs.Four weeks and eight weeks later,compound materials were respectively removed to perform tissue section test.Simultaneously,immunohistochemistry keratin staining was conducted to examine regeneration of epithelial cells.MAIN OUTCOME MEASURE:Biocompatibility of BMSCs and BAM.RESULTS:①BMSCs were cultured by whole bone marrow method.Flow cytometry demonstrated that third passage of cells were positive for CD29(99.43%).②BAM had good biological characteristics.Homogen matrix and byssoid collagen appeared under a microscope.Compatibility trials showed good compatibility of BMSCs and BAM and well-growth cells.③Four weeks later,histological section test confirmed inflammatory cell infiltration,closely-arranged collagen and elastic fiber.Immunohistochemistry keratin staining showed lamellar and discontinuous simple epithelium.Eight weeks later,no inflammatory cell infiltration was found,and closely-arranged collagen and elastic fiber were detected.Immunohistochemistry keratin staining showed lamellar and continuous multiple epitheliums.CONCLUSIoN:With good compatibility,BMSCs and BAM appear to be an ideal material for bladder tissue engineering.
9.A correlation study on mental health and social support of peacekeeping soldiers with suicidal ideation in seven countries
Liyi ZHANG ; Yanling WANG ; Jian GUO ; Hai LIN ; Chunxia CHEN ; Gaofeng YAO
Chinese Journal of Behavioral Medicine and Brain Science 2013;(2):150-152
Objective To explore the correlation between mental health and social support of the seven countries peacekeeping soldiers,and provide theoretical guidance for the peacekeeping soldiers to improve the mental health status.Methods Through random cluster sampling,1143 peacekeeping soldiers were investigated with Chinese Military Mental Health Scale (CMMHS) and Social Support Scale (SSS).Results The total score of CMMHS and depression factor((61.06 ± 3.99),(10.11 ± 1.67)) of the suicidal ideation peacekeeping soldiers were significantly higher than the no-suicidal ideation peacekeeping soldiers ((59.97 ± 3.73),(8.97 ± 1.81))(P < 0.05),CMMHS total score and each factors of the seven countries peacekeeping soldiers were significantly higher than the Chinese soldiers norms (P < 0.05),and the total scores ((28.50 ± 1.69)) of the social support of the suicide idea peacekeeping soldiers was lower than the no-suicidal ideation peacekeeping soldiers ((28.92 ±1.78)) (P<0.05).The obsessive-compulsive factor,anxiety factor,depression factor,phobic anxiety factor,somatization factor,neurastheria factor and interpersonal sensitivity factor of CMMHS were the risk factors arise the mental diseases of the peacekeeping soldiers,especially the depression factor(OR =27.00,x2 =439.46,P < 0.05).The CMMHS total score and each factors had obvious negative correlation with social support scores(r =-0.199 ~0.434,P < 0.05).Analysis of multiple stepwise back displayed that the age,gender,education and social support were main factors of influencing mental health of the seven-country peacekeeping soldiers (age:t =2.428,educational level:t =-3.310,social support:t =1.990,P =0.047 ~ 0.01).Conclusion The suicidal ideation has close relationship with peacekeeping soldiers' psychological disease,and the mental health of the peacekeeping soldiers is influenced by the age,gender,education level,and especially by social support.
10.Optimization on Fermentation and Purification of the Fibrinolytic Enzyme from Stenotrophomonas maltophilia
Gao-Xue WANG ; Chao-Jun LIANG ; Hai-Hong HUANG ; Jian-Fu WANG ; Ju-Lin YUAN ;
China Biotechnology 2006;0(09):-
The optimization on liquid fermentation and purification of the fibrinolytic enzyme from Stenotrophomonas maltophilia(DR-929) was investigated.The results showed the best fermentation are amidulin 2.0%,soya flour 1.0%,yeast extract 0.5%,NaCl 1.0%,CaCl2 0.02%,MgSO4 0.05%,inoculum of 36 hours,fermental time 4d,initial pH 8.0 or 9.0,temperature 25℃,volume of media 30ml,volume of inoculum 5% or 6%.The purification process includes the following steps: removing cells by the centrifugation,25%~70% saturation ammonium sulfate precipitation,HIC with Phenyl FF(high sub),IEC with Q-Sepharose FF,gel filtration chromatography with Superdex 75.SDS-PAGE electrophoresis was used to examine the purification effect,and the results indicated that homogeneous strap in SDS-PAGE and has a molecular weight around 28.3kDa.The purification factor and activity recovery of the fibrinolytic enzyme are 271.5 and 24.5%,respectively.