1.Genetic Research of Gene of Gamma 2 Subunit of Gamma-Aminobutyric Acid Type A Receptor in Pedigrees of Generalized Epilepsy with Febrile Seizures Plus
xiu-hong, CHANG ; xi-shun, HUANG ; jian-ke, WEI
Journal of Applied Clinical Pediatrics 2006;0(15):-
Objective To find the relationship between mutation of gamma 2 subunit of the gamma-aminobatyric acid type A receptor(GABRG2) and generalized epilepsy with febrile seizure plus(GEFS+).Methods Probands of 10 families with GEFS+ were selected,the GABRG2 gene were sequenced.Results We found a single nucleotide polymorphism site,and did not find the reported mutations.Conclusion GABRG2 mutation is not common in Hans of northern China.
3.Expression and effect of secondary lymphoid tissue chemokine in experimental ulcerative colitis in rats
Xi-Mei CHEN ; Bu-Jun GE ; Chang-Qing YANG ; Jian WU ;
Chinese Journal of Digestion 2001;0(09):-
Objective To investigate the expression and effect of secondary lymphoid tissue chemokine(SLC)in experimental ulcerative colitis(UC)in rats.Methods Thirty Spague-Dawley rats were divided into control group and UC group.SLC expression in colon tissues was detected by RT-PCR and immunohistochemistry,respectively.Results The transcriptional level of SLC in UC tissues was significantly higher than that in the control group(0.846?0.07 vs 0.312?0.12,P<0.01).The positive expression of SLC was concentrated mainly on submucosa,and the positive rate of SLC protein expression in UC group significantly higher than that in control group(P<0.01).Conclusion SLC overexpression could contribute to the pathological processes in UC rats,thus SLC may be an ideal ther- apeutic target for UC.
5.Comparison of plasma low-density lipoprotein and oxidized low-density lipoprotein levels with coronary lesion severities in patients with coronary artery disease.
Xi-Min HE ; Ding-Cheng XIANG ; Jian-Xin HE ; Chang-Jiang HONG ; Jian QIU ; Jun MA ; Jin-Xia ZHANG
Chinese Journal of Cardiology 2007;35(5):451-456
OBJECTIVETo explore the relationship between plasma low-density lipoprotein (LDL) and oxidized low-density lipoprotein (ox-LDL) levels and the severity of coronary atherosclerosis.
METHODSFasting plasma ox-LDL was measured by enzyme-linked immunosorbent assay and plasma LDL was measured by biochemical autoanalyser in 31 patients with coronary artery spasm (CAS group, chest pain with positive acetylcholine provocation test but without significant coronary artery stenosis), 35 patients with stable angina pectoris (SAP group) and 24 healthy persons (control group).
RESULTSPlasma LDL levels were similar between CAS and SAP groups but significantly higher than that in control group. Plasma ox-LDL levels significantly increased in proportion to coronary lesion severities [SAP (575 +/- 219 microg/L) > CAS (299 +/- 117 microg/L) > control (218 +/- 35 microg/L)]. In SAP group, plasma ox-LDL level was also significantly higher in multi-vessel disease group than that in single-vessel disease group (672 +/- 92 vs. 462 +/- 72 microg/L, P < 0.05).
CONCLUSIONPlasma ox-LDL but not LDL level is significantly correlated to the severity of coronary atherosclerosis and should therefore be the focused therapy target in patients with coronary artery disease.
Adult ; Aged ; Angina Pectoris ; blood ; classification ; Coronary Vasospasm ; blood ; Female ; Humans ; Lipoproteins, LDL ; blood ; Male ; Middle Aged
6.Discrimination of anticancer agent action loci at G(2) and M phases by flow cytometry and confocal microscopic imaging.
Yi-Sheng ZHONG ; Chang-Chuan PAN ; Chang-Nan JIN ; Jian-Jun LIN ; Gong-Peng XIONG ; Jian-Xi ZHANG ; Jian-Pin GONG
Journal of Experimental Hematology 2009;17(4):965-968
This study was purposed to evaluate a method to discriminate the action loci of anticancer agents in G(2) and M phases of cell cycle. The meta-amsacrine (m-AMSA) and vinblastine (VBL), already known as G(2) and M phase arrest agent respectively, were used to induce the arrest of MOLT-4 cells at G(2) and M phases, the change of DNA content was detected by flow cytometry, the morphology of arrested cells was observed by confocal microscopy so as to find the arrest efficacy difference of 2 anticancer agents. As a result, the flow cytometric detection showed that the arrested MOLT-4 cells displayed the raise of peaks in G(2) and M phases, but flow cytometric detection alone can not discriminate the difference between them. The observation with confocal microscopy showed that the MOLT-4 cells arrested by m-AMSA displayed the morphologic features in G(2) phase, while the MOLT-4 cells arrested by VBL displayed the morphologic features in M phase. This observation with confocal microscopy is helpful to discriminate the difference between them. In conclusion, the combination of flow cytometry with confocal microscopy is one of the effective methods to discriminate the kind of G(2) or M phase arresting agent of anticancer drugs.
Antineoplastic Agents
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pharmacology
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Cell Cycle
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drug effects
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Cell Division
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drug effects
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Flow Cytometry
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G2 Phase
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drug effects
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Humans
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Microscopy, Confocal
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Tumor Cells, Cultured
7.Cell cycle arrest at M phase induced by vinblastine in MOLT-4 cells.
Yi-Sheng ZHONG ; Chang-Chuan PAN ; Chang-Nan JIN ; Jian-Jun LI ; Gong-Peng XIONG ; Jian-Xi ZHANG ; Jian-Ping GONG
Journal of Experimental Hematology 2009;17(2):358-362
This study was purposed to investigate the biological effect of vinblastine (VLS), usually known as inductor of mitotic arrest, on MOLT-4 of ALL cells and to evaluate its significance. The cell arrest in M phase and/or cell apoptosis were induced by treatment of MOLT-4 cells with 0.05 microg/ml VLS for 0 - 12 hours; the DNA histogram was detected by flow cytometry; the morphological changes of cells were observed by confocal microscopy; the cell cycle distribution, cell apoptosis and morphological changes of cells before and after arrest were analyzed by using arrest increasing rate (AIR), arrest efficiency (AE), apoptosis rate (AR) and morphologic parameters respectively. The results indicated that the cell arrest did not accompanied by significant increase of apoptosis rate; the DNA histogram of cell arrest showed dynamic change of cell cycle in time-dependent manner; the arrest efficiency could be quantified. The cell arrest at M phase was accompanied by cell stack in S phase, the cell proliferation rate dropped after cell arrest occurred. The cells arrested at M phase possessed of characteristic morphologic features in cell mitosis. It is concluded that the vinblastine can solely induce arrest of MOLT-4 cells at M phase. This study provides experimental basis for further investigating the relation of cell cycle arrest to apoptosis, mechanism of checkpoint and development of new anticancer drugs.
Apoptosis
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drug effects
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Cell Cycle
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drug effects
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Cell Division
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drug effects
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Flow Cytometry
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Humans
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Tumor Cells, Cultured
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Vinblastine
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pharmacology
8.Changes of pathogens and susceptibility to antibiotics in hematology ward from years 2001 to 2005.
Yun FAN ; Nai-Bai CHANG ; Yun-Jian HU ; Xiao-Man AI ; Shao-Quan XU ; Jiang-Tao LI ; Xi-Chun GU
Journal of Experimental Hematology 2008;16(6):1455-1458
The purpose of this study was to determine the changes of pathogens in hematological ward and susceptibility of patients received chemotherapy to antibiotics. The pathogens were taken from blood, urine and sputum of patients who accepted chemotherapy from years 2001 to 2005, then were isolated and identified. The susceptibility test was performed by disk diffusion method. The results showed that the total of 418 strains were detected. Gram-negative bacteria were the most common of nosocomial infection. Pseudomonas aeruginosa, Enterobacter cloacae, E. coli account for the most of Gram negative- bacteria infection and most resistant to broad-spectrum penicillin, Acinetobacter baumannii showed a trend of increase. The ratios of gram positive bacteria and fungi were increased slowly, mainly as Enterococcus and Candida. Enterococcus is the most common cause of Gram-positive bacterial infection. Vancomycin resistance did not occur. It is concluded that Gram-negative bacteria are main cause of nosocomial infection in patients with hematological malignancies. Gram positive bacteria and fungi had been more frequent. Strains resistant to antimicrobial agents increase.
Cross Infection
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epidemiology
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microbiology
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Drug Resistance, Bacterial
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Gram-Negative Bacteria
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drug effects
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isolation & purification
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Gram-Negative Bacterial Infections
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epidemiology
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microbiology
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Hematologic Diseases
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microbiology
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Hematologic Neoplasms
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microbiology
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Humans
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Microbial Sensitivity Tests
9.Role of secondary lymphoid tissue chemokine in the pathogenesis of rat ulcerative colitis.
Bu-jun GE ; Xi-mei CHEN ; Chang-qing YANG ; Jian WU
Chinese Journal of Gastrointestinal Surgery 2008;11(6):561-564
OBJECTIVETo investigate the effect of secondary lymphoid tissue chemokine (SLC) on experimental colon lesions in rats with ulcerative colitis.
METHODSSixty Sprague-Dawley rats were randomly divided into control group, model group and SLC intervention group. Colonic mucosal lesions of different groups were observed with HE staining for inflammation and lymphocyte homing situation. Cytokine IL-2 and IL-6 levels were measured by ABC-ELISA. Semi-quantitative RT-PCR was used to examine the colonic SLC expression.
RESULTSIntestinal inflammation score and colonic cytokine levels were significantly different among three groups (P<0.05, P<0.01). Abnormal lymphocyte homing phenomenon under colonic mucosa was found in the model group and the intervention group. SLC mRNA expression of the model and intervention groups increased significantly compared with the control group (0.846+/-0.047, 0.768+/-0.135 vs 0.312+/-0.112, P<0.01). However, there was no significant difference between model group and intervention group.
CONCLUSIONSSLC may play an important role in experimental colonic mucosal inflammation in rats with ulcerative colitis. Blockade of SLC may be one of effective ways in reducing colonic mucosal inflammation.
Animals ; Chemokine CCL21 ; metabolism ; Colitis, Ulcerative ; metabolism ; physiopathology ; Female ; Inflammation ; Interleukin-2 ; metabolism ; Interleukin-6 ; metabolism ; Rats ; Rats, Sprague-Dawley
10.Intervention of nutritional status and hypoxia endurance by a nutritional supplement in young adults living at high altitude.
Jing-yu WEI ; Chang-jiang GUO ; Ji-jun YANG ; Yin-zhi XIE ; Jian-hua CUI ; Xi-zhou ZHANG ; Bao-yu LUO
Chinese Journal of Applied Physiology 2007;23(2):150-153
AIMTo investigate the effects of a nutritional supplement on nutritional status and hypoxia endurance in young adults living at high altitude.
METHODSForty healthy male young adults were recruited and randomly assigned to control and intervention groups. The nutrition survey was carried out using weighing method. The intervention group was given a nutritional supplement specifically designed for use at high altitude, while the control group was treated with a supplement made of stir-fried flour. After 20 days of supplementation, they marched from the altitude of 3700 m to 5100 m. The changes in HR, SaO2, serum concentrations of VA and VB2 and some minerals were measured.
RESULTSThe results of nutrition survey showed that the ratio of three macronutrients was not adequate and the intakes of calcium, VA and VB2 were below Chinese RNI. The serum concentrations of calcium, magnesium and VA were below normal references. The serum VB2 concentration was at the low level o f normal reference. The nutritional supplement could increase the serum concentrations of calcium, magnesium, VA and VB2, indicating an improved nutritional status. The changes in HR and SaO2 were diminished in intervention group compared with control group.
CONCLUSIONThe nutritional supplement can improve nutritional status and increase the hypoxia endurance in young adults living at high altitude.
Adult ; Altitude ; Dietary Supplements ; Humans ; Hypoxia ; prevention & control ; Male ; Nutritional Status ; Vitamins ; therapeutic use