1.Gastric adenocarcinoma associated with myelolipoma of parietal pleura: a case report.
Dong-sheng ZHANG ; Dong-hai LI ; Hai-xia BI ; Xiao-feng WU
Chinese Journal of Pathology 2006;35(7):437-437
Adenocarcinoma
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pathology
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surgery
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Biopsy
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Diagnosis, Differential
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Gastric Fundus
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pathology
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surgery
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Humans
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Male
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Middle Aged
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Myelolipoma
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pathology
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surgery
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Neoplasms, Multiple Primary
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pathology
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surgery
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Pleural Neoplasms
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pathology
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surgery
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Stomach Neoplasms
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pathology
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surgery
2.Roles of theaflavins in inflammatory airway mucus hypersecretion
hai-qiao, WU ; yang-ping, DING ; xiang-dong, ZHOU
Journal of Shanghai Jiaotong University(Medical Science) 2006;0(02):-
Objective To investigate the roles of theaflavins(TFs) in airway mucus hypersecretion induced by human neutrophil elastase(HNE). Methods Human lung adenocarcinoma cell A549 was stimulated by HNE for mucus hypersecretion,and TF monomers(TF1,TF2 and TF3) were used for intervention.The effects of TF monomers on viability of A549 cells were examined by MTT method.After the effective doses of TFs were determined,A549 cells were divided into 4 groups for experiment.In control group,A549 cells were cultured with serum-free medium.In HNE treatment group,A549 cells were treated with HNE(50 nmol/L) for 24 h.In TF monomer intervention groups,A549 cells were pre-treated with TF1,TF2 or TF3(50,100 or 200 ?g/mL) for 24 h,and were then treated with HNE for another 24 h.In AG1478 intervention group,A549 cells were pre-treated with AG1478(5 ?mol/L),an epidermal growth factor receptor blocker for 30 min,and were then treated with HNE for another 24 h.The changes in mucin(MUC) after treatment by different doses of TF1,TF2 and TF3,and by TF3(200 ?g/mL) for different time(12 h,24 h and 36 h) were detected.The changes in MUC5AC mRNA expression and MUC5AC protein expression were detected by RT-PCR and ELISA,respectively. Results The MUC5AC mRNA expression and protein expression in HNE treatment group were significantly higher than those in control group(P
3.Effect of flunarizine on the epileptiform discharges in cortex and hippocampus of rat with penicillin induced epilepsy.
Guo-feng WU ; Shi-hai SHAN ; You-zhong DONG
Chinese Journal of Applied Physiology 2004;20(2):179-204
Animals
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Cerebral Cortex
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drug effects
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physiology
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Epilepsy
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chemically induced
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physiopathology
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Female
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Flunarizine
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pharmacology
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Hippocampus
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drug effects
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physiology
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Male
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Penicillins
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adverse effects
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Rats
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Rats, Wistar
4.A Comparison of Treatment of Tic Disorder with Risperidone and Haloperidol
Yao-dong LI ; You-nian LUO ; Hai-shan WU ; Shuhan LUO ; Huijie OUYANG
Chinese Journal of Rehabilitation Theory and Practice 2006;12(10):844-845
ObjectiveTo explore the efficacy and safety of risperidone and haloperidol in treating Tic disorder.Methods78 patients with Tic disorder were randomly divided into the risperidone group and haloperidol group with 39 cases in each group and treated with risperidone and haloperidol respectively for 8 weeks. All patients of two groups were assessed with the Clinical Global Impression Scale (CGI) and Treatment Emergent Symptom Scale (TESS) before treatment and at the end of the 2nd, 4th and 8th week after treatment. Dosages of patients of two groups were recorded.ResultsAfter 8 weeks treatment, the average maximum dosage of risperidone was (1.4±0.34)mg, and that of haloperidol was (7.3±0.52)mg. The total effective rate of risperidone group was 82% and that of haloperidol group was 82.3 %. There was no significant difference between two groups ( P>0.05). The incidence of adverse reactions in risperidone group was 28.2%, and that in haloperidol group was 76.9%. There was a significant difference between two groups (P<0.01), especially at the end of 2nd week after treatment.ConclusionRisperidone and haloperidol both are effect on Tic disorder, but safety and compliableness of risperidone are higher.
5.Phylogenetic analysis for Fritillaria hupehensis: evidence from ITS, rpl16 and matK sequences.
Hong-wu LAI ; Yao-dong QI ; Hai-tao LIU ; Jiu-shi LIU ; Ben-gang ZHANG
China Journal of Chinese Materia Medica 2014;39(17):3269-3273
The systematic position of Fritillaria hupehensis has been in dispute. Phylogentic analyses were conducted on sequences of ITS, rpl16, matK sequences for species of F. hupehensis and allies. Lilium davidii was designed as outgroup. The analyses were performed using MP and ML methods. Conclusions could be achieved as follow. The topologies of MP and ML are consistent. The samples of F. hepehensis from different places form a supported clade with a strong bootstrap. And then form a strongly supported clade with F. anhuiensis, F. monantha. The results suggests that although F. hupehensis has a closet relation with the two ones, it exists some difference.
DNA, Plant
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chemistry
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genetics
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DNA, Ribosomal Spacer
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genetics
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Endoribonucleases
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genetics
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Fritillaria
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classification
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genetics
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Molecular Sequence Data
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Nucleotidyltransferases
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genetics
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Phylogeny
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Plant Leaves
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genetics
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Ribosomal Proteins
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genetics
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Sequence Analysis, DNA
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Species Specificity
6.Mutation analysis of a Chinese family with Alport syndrome and genetic diagnosis before embryo implantation
Hui ZHANG ; Dong WU ; Litao QIN ; Weili SHI ; Hongdan WANG ; Hai XIAO ; Shixiu LIAO
Chinese Journal of Applied Clinical Pediatrics 2015;30(5):362-364
Objective To study the gene mutation of a Chinese family with Alport syndrome and to perform preimplantation genetic diagnosis before embryo implantation.Methods Next generation sequence analysis was done for checking COL4A3,COL4A4 and COL4A5 genes in the Alport syndrome family members.Array comparative genomic hybridization(CGH) was used to detect the embryos.Results A mutation c.2605G > A was found and identified in COL4A5 gene of all of the Alport syndrome patients in the family,but COL4A3 and COL4A3 genes were normal in all of the detected people.After searching for the mutation database,the mutation c.2605G > A of COL4A5 gene was related to the X-linked dominant Alport syndrome.Three embryos were detected by using the preimplantation genetic diagnosis.Among these embryos,there were two male and one female.One of the male embryos was chromosomal aneuploidy,which was 45,XY,-16 and the other was normal.This normal embryo was implanted,and after 20 weeks the prenatal amniocentesis diagnosis approved that the fetus was normal.Conclusions The mutation of COL4A5 gene (c.2605 G > A) is the cause of Alport syndrome in this family,which indicates that next generation sequence analysis proves to be an accurate and rapid method to detect Alport syndrome disease.Meanwhile array CGH can be used to reduce birth rates as a useful preimplantation genetic diagnosis method.
7.The intervention-therapeutic effect of lipiodol-arsenic trioxide emulsion for primary hepatic carcinoma
Xiang-Dong LIU ; Wen-Juan WU ; Hai-Tao LI ; Xin-Yun FAN ; Yue-Ming NAN ;
Journal of Interventional Radiology 2006;0(12):-
Objective To discuss the short-term clinical effect including functional change of lipiodol- arsenic trioxide emulsion on the primary hepatic carcinoma.Methods Fifty-two patients undergone arterial chemoemblization were selected and then randomly divided into two groups:treatment group(n=27)and control group(n=25).Patients in treatment group were treated with lipiodol-arsenic trioxide,while those in control group treated with mitomycin,epirubicin,cisplatin or lipiodol.Clinical symptoms and six liver function parameters were observed and analized.Results The clinical symptoms of patients in treatment group improved much better than those in control group,and the liver function impairment of patients in treatment group also decreased more than those in control group.Conclusions Lipiodol-arsenic trioxide is an effective and safe intervention-therapeutic embolization material for primary hepatic carcinoma.
8.Adult-onset Still's disease and acute severe hepatic lesion
Li MA ; Zhi-Ji QIAN ; Meng-Jun ZHAO ; Dong-Hai WU ;
Chinese Journal of Rheumatology 2003;0(08):-
1000 IU/L,TBil 40~250 mg/L,and mild liver dysfunction at beginning of the disease,but acute severe hepatic lesion occurred due to the use of antibiotics,immunodepressant or NSAIDs.Three patients developed liver function failure and died,7 patients' liver function recovered to nor- mal by increasing dosage of glucocorticoid.Conclusion AOSD with mild liver dysfunction is frequently en- countered.During the treatment,acute severe hepatic lesion may occur due to certain drugs.Therefore,any drug used in AOSD with mild liver dysfunction should be cautious.Once acute severe hepatic lesion happens, increases the dosage of glucocorticoid promptly can improve prognosis.
9.Effects of biphasic square waveform with different energy levels on external defibrillation
Hai-Dong WU ; Zi-Tong HUANG ; Tong WANG ; Yue FU ; Long-Yuan JIANG ;
Chinese Journal of Emergency Medicine 2006;0(09):-
Objective To compare the effects of biphasic square waveform (BSW) with low or high energy on external defibrillation.Method Adult swine model of closed chest ventricular fibrillation induced by electricity was established.Eighteen swine,weighing (30?3.3) kg were randomly divided into three groups:50-50-50 J group (n=6),30-50-75 J group (n=6),120-150-200 J (n=6).After three minutes of ventricular fibrillation without treatment,the pigs in the three groups were defibrillated accordance to the above sequences. Results 30 J BSW didn't succed to external defibrillate.The first defibrillation successful rate of 50 J and 120 J BSW was 5/6.The total defibrillation successful rate of every group was 100%.All pigs quickly had spontaneous circulation after defibrillation and survived more than 24 hours.ST-T change of low-energy was less than that of high-energy.After resuscitation,myocardial function decreased,but there had not significant differences between groups.Conclusions In the study,30J BSW could not reach successful defibrillation,and 50 J and 120 J BSW had similar defibrillation efficacy.The ideal energy of BSW external defibrillation was 50 J.
10.Heterozygous TP63 mutation in a Chinese patient with ectrodactyly-ectodermal dysplasia clefting syndrome without clefting.
Dong HAN ; Hua WU ; Xiao-xia ZHANG ; Hai-lan FENG
Chinese Journal of Stomatology 2010;45(12):767-769
OBJECTIVETo determine if alteration in TP63 is responsible for a Chinese patient with ectrodactyly-ectodermal dysplasia clefting (EEC) syndrome, but without cleft palate/lip.
METHODSScreening of TP63 gene was performed in the patient with EEC syndrome and his family members using PCR-single strand conformational polymorphism (SSCP) analysis, then performed by direct sequencing of the coding region.
RESULTSA C > T substitution at nucleotide position 838 in exon 7 was detected in the patient, and the change predicted a heterozygous missense mutation, Arg280Cys. His parents showed the wild type.
CONCLUSIONSThe results indicate that the de novo mutation Arg280Cys of the TP63 gene observed in the patient maybe contribute to his EEC syndrome.
Asian Continental Ancestry Group ; Cleft Lip ; genetics ; Cleft Palate ; genetics ; Ectodermal Dysplasia ; genetics ; Exons ; Genotype ; Heterozygote ; Humans ; Mutation, Missense ; Transcription Factors ; genetics ; Tumor Suppressor Proteins ; genetics