1.Relationship between Simple Obesity and Fibrinogen,B?448 G/A Gene Polymorphism in Children
jie, GAO ; feng-zhen, ZHAO ; jun-ling, ZHANG ; ying, WU ; hong-fen, LI
Journal of Applied Clinical Pediatrics 2006;0(19):-
0.05).The FMPV of the B?448 AA plus GA was higher than that of the GG type in obesity group(P0.05).Conclusions The simple obesity in children is associated with Fg and FMPV,which have become the high risk factors of the disease of heart and brain.The Fg B?448 G/A gene polymorphism may be an accumulative efficiency gene of children with simple obesity by influencing FMPV.
2.Anti-tumor mechanism of active components from extract of Actinidia rufa root.
Guo-biao LIN ; Zhen-guo ZHONG ; Wen-yan ZHANG ; Feng-fen ZHANG ; Xi-hui CHEN ; Chu-sheng HUANG
China Journal of Chinese Materia Medica 2008;33(16):2011-2014
OBJECTIVETo observe effect and mechanism of n-Butanol lysate of alcohol extracts from Actinidia rufa root (monomer of R6,R8).
METHODTunel, Wright's stain with Giemsa's stain dyeing, and Hoechst 33258-PI double dyeing assay were used to detect the apoptosis of SGC7901 tumor cells treated with R6, R8. The SGC7901 tumor cells were randomly divided into control group and two treatment groups administered 0.05 g x L(-1) R6, R8, respectively, for 72 h). FCM assay was used to detect the apoptosis. Agarose electrophoresis assay was used to detect DNA strand break of tumor cells and reveal anti-tumor action mechanism.
RESULTThe apoptosis percentage of the tumor cell in 24 h, 48 h, 72 h was (17.08 +/- 2.78)% , (29.68 +/- 2.96)%, (52.46 +/- 3.81)%; (14.75 +/- 2.14)%, (27.35 +/- 3.79)%, (45.64 +/- 5.24)%, respectively, for the treatment group, significantly higher than that in the control group (1.94 +/- 1.55)%, (2.78 +/- 1.84)%, (11.8 +/- 2.79)% (P < 0.01) by tunnel assay. Wright's stain with Giemsa's stain dyeing assay, Hoechst 33258-PI and FCM double dyeing assay showed same action. R6 and R8 had the effect of inducing the DNA histogram of tumor cells (P < 0.01).
CONCLUSIONThe anti-tumor mechanisms may be associated with inducing the injury of DNA and stimulating apoptosis.
Actinidia ; chemistry ; Apoptosis ; drug effects ; Cell Line, Tumor ; Drugs, Chinese Herbal ; chemistry ; pharmacology ; Flow Cytometry ; Humans ; Immunohistochemistry ; Plant Roots ; chemistry
3.Expression of matrix metalloproteinase-2 and-9 in kidney of diabetic rats.
Feng-qin DONG ; Hong LI ; Wei-min CAI ; Jun TAO ; Fen-ping ZHEN ; Zhe ZHANG
Journal of Zhejiang University. Medical sciences 2004;33(3):245-249
OBJECTIVETo investigate the expression of matrix metalloproteinase-2 (MMP-2), matrix metalloproteinase-9(MMP-9), transforming growth factor beta(1)(TGF-beta(1)) and IV-collagen (C-IV) in kidneys of diabetic rats.
METHODSRat diabetic model was induced by streptozotocin (70 mg/kg), and kidneys were examined pathologically and the expressions of MMP- 2, MMP-9, TGF-beta(1) and C-IV were studied by immunohistochemistry. The results were analyzed by imaging quantitative analysis technique.
RESULTImmunoreactive MMP-2 and MMP-9 were mainly expressed in the mesangial cells, endothelial cells, parietal layer of Bowman's capsule and tubular cells. The expression of MMP-2 was significantly weaker in the glomeluri of diabetic rats than that of the control animals (P<0.05), while the expression of TGF-beta(1) and C-IV in the glomeluri of diabetic rats was significantly stronger than that of the controls (P%lt;0.05). The expression of MMP-9 didn't show significant different in glomeluri of the two groups (P>0.05).
CONCLUSIONExpression of MMP-2 in glomeluri is decreased in diabetic rats, which may be related to the increased TGF-beta(1) and in turns promote the accumulation of C-IV.
Animals ; Collagen Type IV ; analysis ; Diabetes Mellitus, Experimental ; enzymology ; pathology ; Female ; Immunohistochemistry ; Kidney ; enzymology ; pathology ; Male ; Matrix Metalloproteinase 2 ; analysis ; Matrix Metalloproteinase 9 ; analysis ; Rats ; Rats, Sprague-Dawley ; Transforming Growth Factor beta ; analysis ; Transforming Growth Factor beta1
4.Preliminary report of laryngeal preservation in the surgical salvage of recurrent laryngeal cancer
Xiao-Ming LI ; Bin DI ; Zhen-Feng TAO ; Qi SONG ; Shu-Fen XIAO ; Hong-Xia LI ; Yong-Liang SHAO
Chinese Journal of Otorhinolaryngology Head and Neck Surgery 2012;47(7):532-535
Objective To explore the plausibility of laryngeal preservation in salvage surgery of recurrent laryngeal carcinoma.Methods Comprehensive clinical and radiological assessments on a specific group of patients with recurrent laryngeal cancer and their relapsed tumors were carried out to determine the methods and indications of salvage surgery for preservation of laryngeal functions.Salvage surgery with preservation of larynx was performed in a selective of 36 laryngeal cancer patients with relapsed tumors in their larynges after radiotherapy or partial laryngectomies.All patients were regularly followed up after discharge from the hospital. Postoperative survival was calculated by Kaplan-Meier's method.Results Among various laryngeal preservation regimens given,a second transoral laser surgery was carried out in 4 cases,horizontal hemilaryngectomy in 4 cases,vertical hemilaryngectomy in 13 cases and Majer-Piquet's operation in 15 cases,respectively.Simultaneous neck dissection was conducted in 18 cases.Postoperative complications were encountered in 6 cases,most common of which were local infection and laryngeal fistula with no hospital mortality and other major morbidities.Five cases with immediate postoperative complicatios were cured with proper management.The remained one case undergone vertical partial laryngectomy for recurrence after tumor resection via laryngeal fissure received postoperative radiation due to positive surgical margin,and complicated laryngeal atresia and obstruction with loss of his laryngeal functions, Local recurrence was observed in 5 cases and simultaneous locoregional recurrence was seen in 1 case,with the resulting local control rate of 83.3% (30/36).The 3-year postoperative survival rate was 80.6%.The cause of death was tumor recurrence in 3 cases,distant metastasis in 3 cases and non-tumor-associated disease (heart attack) in 1 case,respectively.Conclusions Salvage surgery with laryngeal preservation can be carried out in the selected cases with early or locally-confined recurrent lesions within the larynx,on the condition that the recurrent tumors be assessed thoroughly and indications for associated surgical techniques be evaluated properly.
5.Effect of tigecycline on multidrug resistant Acinetobacter baumannii adeB gene expression and its clinical significance
Yu-Feng DING ; Shi-Fen LIU ; Zhen-Tian CHENG ; Pan-Fei HOU
The Chinese Journal of Clinical Pharmacology 2015;(20):2024-2026
Objective To investigate the effect of tigecycline on multi-drug resistant Acinetobacter baumannii ( MDR -AB ) adeB gene expre-ssion and its clinical significance.Methods A total of 60 clinical iso-lates of multidrug-resistant Acinetobacter baumannii were selected, from which 15 experimental strains with positive result to ciprofloxacin ( CIP) efflux pump encoded gene were screened.The minimum inhibitory con-centration ( MIC) before and after given tigecycline was determined using agar dilution assay, the gene of the strains with large change of MIC value was sequenced and compared.Results The lowest MIC of tigecy-cline to MDR-AB was 2 mg? mL-1 .The MDR-AB′s MIC of tigecy-cline at concentration of 0 , 0.62 mg? mL-1 and ciprofloxacin at 1.25 , 2.5 mg? mL-1 were significantly different ( P<0.05).After tigecycline treatment, adeB gene segment had 15 bases mutation, 5 amino acids are replaced and 4 mutant amino acid had no substitution.The adeB gene expression levels before and after the treatment of tigecyclin were (2.51 ±0.72) and (0.87 ±0.21), statistically significant (P<0.05). Conclusion Tigecycline inhibits MDR -AB efflux pump adeB gene expression, lowers adeB expression levels. Other agents with its combination for the treatment of MDR-AB might improve the clinical efficacy.
6.Epidemiological surveillance of leptospirosis in 1997-2002 in Zhejiang Province.
Zhen-yu GONG ; Li-peng JIANG ; En-fu CHEN ; Zhen WANG ; Jun-fen LI ; Gui-ming FU ; Cheng-liang CAI ; Feng-hua XU
Chinese Journal of Epidemiology 2004;25(12):1091-1091
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7.Coxsackie virus B types were discriminated by RT-PCR.
Zhen-yong LI ; Zhi-tao LI ; Yan-ming FENG ; Da-xiao SHAO ; Da-peng ZHAO ; Tian-xing CUI ; Guo-cui YANG ; Ling-bo QU ; Yu-fen ZHAO
Chinese Journal of Experimental and Clinical Virology 2004;18(3):291-293
OBJECTIVETo develop a method for detection of coxsackie B virus type 1-6 by RT-PCR.
METHODSA pair of primers were designed to amplify all types of coxsackie B virus 1-6 efficiently. The PCR product was hybridized in micro-wells in which 6 type specific oligonucleotide probes had been coated respectively, colorimetric detection was performed to discriminate the types of coxsackie B virus.
RESULTSThis method was shown to be concordant with the IgM ELISA, 71.7% of anti-coxsackie B positive cases could be detected by RT-PCR.
CONCLUSIONThe RT-PCR method can type coxsackie B virus efficiently and provides a tool for clinical diagnosis and epidemiological investigation.
DNA Primers ; Enterovirus B, Human ; classification ; genetics ; isolation & purification ; Enterovirus Infections ; diagnosis ; virology ; Enzyme-Linked Immunosorbent Assay ; Humans ; Immunoglobulin M ; blood ; Reverse Transcriptase Polymerase Chain Reaction ; methods
8.Family-based association study of XRCC1 gene polymorphisms in nasopharyngeal carcinoma.
Qing-Hua PAN ; Yun CAO ; Jin-Fen XU ; Li-Zhen CHEN ; Qi-Sheng FENG ; Yi-Xin ZENG ; Wei-Hua JIA
Chinese Journal of Preventive Medicine 2007;41 Suppl():12-16
OBJECTIVETo test the association between XRCC1 gene polymorphisms and susceptibility of nasopharyngeal carcinoma in Cantonese nuclear families through a family-based association study.
METHODSA total of 2134 study subjects from 457 Cantonese nuclear families were recruited in the study. Each family had two parents and at least one offspring with nasopharyngeal carcinoma. Genotyping for three single nucleotide polymorphisms in XRCC1 gene, including rs1799782 (C > T), rs25489 (G > A) and rs25487 (G > A), were performed with PCR-RFLP assay. The genotype data were analyzed with family-based association test (FBAT) software to check linkage and association between the three genetic markers and susceptibility of nasopharyngeal carcinoma.
RESULTSFBAT analysis showed XRCC1 gene genotypes and haplotypes were not significantly associated with nasopharyngeal carcinoma in our study population (rs1799782: chi(2) = 1.006, P = 0.605; rs25489: chi(2) = 0.470, P = 0.790; rs25487: chi(2) = 2.563, P = 0.278; haplotype: chi(2) = 3.004, P = 0.557, global statistic). For rs25487, the G allele (major allele) showed increased transmission under dominant model (Z = 1.985, P = 0.047). Whereas the C allele (minor allele) exhibited reduced transmission under recessive model (Z = -1.985, P = 0.047). However, no increased/reduced transmission was observed under additive model and with global statistic.
CONCLUSIONThere is no evidence of an association between polymorphisms in XRCC1 gene and susceptibility of nasopharyngeal carcinoma in Cantonese nuclear families is observed in this study.
DNA Damage ; DNA Repair ; DNA-Binding Proteins ; genetics ; Gene Frequency ; Genotype ; Humans ; Nasopharyngeal Neoplasms ; genetics ; Pedigree ; Polymorphism, Single Nucleotide ; Surveys and Questionnaires ; X-ray Repair Cross Complementing Protein 1
9.Determination of SARS-CoV by simplified nested fluorescent RT-PCR.
Zhen-yong LI ; Da-xiao SHAO ; Zhi-tao LI ; Yan-ming FENG ; Jian-zhou JING ; Qui-qi WANG ; Yun-long WANG ; Ling-bo QU ; Yu-fen ZHAO
Chinese Journal of Experimental and Clinical Virology 2005;19(2):176-178
OBJECTIVETo establish a simple rapid and sensitive nested RT-PCR method for detection of SARS coronavirus RNA by designing the specific primers for SARS and optimizing the parameters for PCR.
METHODSPrimers and fluorescent probes were designed according to the sequences of SARS coronavirus genes available from GenBank. The optimization of the parameters for PCR was performed in PE 7700 thermal cycle. The 36 serum samples and 40 mouthwash of SARS patients and 80 samples of healthy people were tested.
RESULTSThe positive rate of patient serum and mouthwash was 33.6%, (12/36) and 67.5%, (27/40), respectively, while the positive rate of healthy people was zero (0/160).
CONCLUSIONThe simple nested RT-PCR method was a rapid, efficient and sensitive one for SARS early diagnosis.
Bodily Secretions ; virology ; DNA Primers ; Humans ; RNA, Viral ; blood ; genetics ; Reproducibility of Results ; Reverse Transcriptase Polymerase Chain Reaction ; methods ; SARS Virus ; genetics ; Sensitivity and Specificity ; Severe Acute Respiratory Syndrome ; blood ; diagnosis ; virology
10.Effects of the Panax notoginseng saponins on the level of synaptophysin protein in brain in rat model with lesion of Meynert.
Zhen-Guo ZHONG ; Ze-Qiang QU ; Nai-Ping WANG ; Feng-Fen ZHANG ; Wen-Yan ZHANG ; Uzhong-Peng LU
China Journal of Chinese Materia Medica 2005;30(12):913-915
OBJECTIVETo observe the protective effect of Panax notoginseng saponins (PNS) on the level of synaptophysin ptotein in brain in rat model with Alzheimer's disease (AD).
METHODThe AD rat models were established by intra-peritoneal injection of D-galactose combined with excitatory neurotoxin ibotenic acid injection into bilateral nbM. The activity and content of synaptophysin protein in brain were determined by immunohistochemistry analysis.
RESULTPNS could reduce the lesion of level of synaptophysin protein in brain, as compared with those of model group's rats.
CONCLUSIONPNS plays a protective role by reducing down of the level of synaptophysin protein in brain in lesion of AD animal model.
Alzheimer Disease ; chemically induced ; metabolism ; pathology ; Animals ; Basal Nucleus of Meynert ; drug effects ; pathology ; Brain ; metabolism ; pathology ; Galactose ; toxicity ; Ginsenosides ; isolation & purification ; pharmacology ; Ibotenic Acid ; toxicity ; Neuroprotective Agents ; isolation & purification ; pharmacology ; Panax ; chemistry ; Plants, Medicinal ; chemistry ; Rats ; Rats, Wistar ; Synaptophysin ; metabolism