1.Study on Glycolic Acid Oxidase (GO) of Spirulina(Arthrospira)
Zhi-Zhong WANG ; Dong-Hui GONG ; Hua LIU ; Chen QIAO ;
Microbiology 1992;0(04):-
A comparative study on the glycolic acid oxidase (GO) of the domestic Spirulina(Arthrospira) platensis (S_(1)) from alkaline lake in Erdos Plateau and the imported S. (A.) platensis (S_(2)) and S. (A.) maxima (S_(3)) as well is made with colorimetric method. The results show that activity of GO (25℃, pH 8.0) of S_(1), S_(2 )and S_(3) is 70.9 U/gFW, 59.6 U/gFW and 80.9 U/gFW respectively; the GO's optimum temperature of S_(1)、S_(2) and S_(3 )is 30℃; the GO's optimum pH value of S_(1 )is 8.6,while that of S_(2 ) 8.2 and that of S_(3) 8.4; the GO of S_(1 )is stable from 0℃ to 35℃ and from pH 7.6 to pH 10.0, while that of S_(2) from 0℃ to 30℃ and from pH 8.0 to pH 9.0 and that of S_(3) from 0℃ to 35℃ and from pH 8.0 to pH 8.6. Adaptive range of S_(1) GO for temperature and pH is wider, and activity at low and high temperature and under strong acidand alkali conditions is higher than that of the imported species.
2.The change of calcitonin gene-related peptide immunoreactive nerve fibers in acute inflammatory pulpitis in rats
Zhi-Zhong CAO ; Jun LIU ; Zhong-Hua ZHOU ; Hui YE ; Wei-Zhong TANG
Academic Journal of Second Military Medical University 2001;22(5):459-460
Objective:To investigate the changes of calcitonin gene-related peptide immunoreactive (CGRP-IR)nerve fibers in rat dental pulps during acute inflammation. Methods: Rat acute pulpitis model was established by silk thread ligation and the change of CGRP-IR nerve fibers was observed with immunohistochemical method.Results: In radical pulp,the CGRP-IR nerve fibers became denser and more heavily stained;in the coronal pulp,the number of CGRP-IR nerve fibers decreased,but the background staining was heavier. Conclusion: During acute inflammation,the amount of CGRP increases in dental pulps, and is released into the surronding tissue in a large scale in the coronal region.
3.Water arsenic, fluoride and chloride detection capability assessment of the drinking water monitoring Labs in Guangdong province
Zhi-xiong, ZHONG ; Li-ping, LIU ; Bing-hui, ZHU ; Chang-yun, HE ; Zhi-bin, LUO ; He-yan, WU
Chinese Journal of Endemiology 2011;30(4):453-455
Objective To assess the proficiency of water monitoring laboratory at rural, county, and provincial levels in Guangdong province, to ensure the province's drinking water monitoring results accurate and reliable. Methods State quality of certified reference materials as water arsenic, fluoride and chloride of 90 copies each were numbered and distributed to 90 monitoring laboratories in the province for testing, The measurement results of the participatory labs were evaluated through normative values and expanded uncertainty, and were compared with those of robust statistics method. Results All participatory labs had timely feedback of their measurement results. The qualified rate was higher when arsenic was tested by hydride generation atomic fluorescence spectrometry and zinc-new silver salt of sulfuric acid spectrophotometric system, while fluoride and chloride by ion chromatography. The average qualified rates of water arsenic, fluoride and chloride of the province's rural drinking water quality monitoring laboratory were 66% (59/90), 72% (65/90) and 72% (65/90), respectively.Seven participatory labs failed the proficiency testing of all three analytes and unqualified rate was 7.8% (7/90)among the ninety participated monitoring labs. The qualified rates of robust statistics method for arsenic fluoride and chloride were greater than those evaluated by the expanded uncertainty, and large deviations with small sample sizes. Conclusions The testing ability of drink-water monitoring labs in Guangdong province has improved.However, by comparison with the requirements of national quality control and testing skills, there is still a gap. It is suggested that internal quality control be included in routine inspeetion to improve laboratory testing technology.
4.Analysis of High Risk Factors for Metabolic Syndrome in Obese Children with Acanthosis Nigricans
ling, YANG ; hui-min, SU ; zhong-shu, ZHOU ; zhi-xin, ZHANG
Journal of Applied Clinical Pediatrics 2004;0(08):-
Objective To explore the high risk factors of metabolic syndrome(MS) in obese children with acanthosis nigricans.Me-thods Body mass index(BMI),blood lipid including triglyeride(TG) and cholesterol(CHO),low density lipoprotein-cholesterol(LDL-C),blood pressure,the level of fasting blood glucose(FBG) and 2 h after oral glucose tolerance test blood glucose(OGTT 2h BG) and the level of fasting insulin(FINS) and 2 h after oral glucose tolerance test insulin (OGTT 2h INS) and homeostasis model appraisal insulin resis-tance index(HOMA-IR) were measured and compared between 25 obese children with acanthosis nigricans[male 15,female 10;aged 8.4-16.0,mean 10.6 years old,weight (72.11?17.66) kg;height (155?14) cm]and 32 normal healthy children[male 18,female 14;aged 7.6-15.8,mean 9.8 years old]in department of pediatric during 1 year.HOMA-IR were also analyzed.Ultrasonic inspections for liver were performed in those children.Results BMI,TG,LDL-C and blood pressure in the obese group were significantly higher than those in the normal control group(Pa0.05).Eighty-four percent of patients in obese children with acanthosis nigricans were diagnosed adiposis hepatica by ultrasonograph.Conclusions The increasing BMI,insulin resistance,blood lipid disorder and blood pressure increase in obese children with acanthosis nigricans are the high risk factors of MS,the close followed-up and treating this kind of obese children can acquire MS early and be helpful to postpone the progress of diabetesⅡ and cardiovascular diseases.
5.Influence of Angelica Sinenisis Injection on Bone Marrow Histology and Ultrastructure in Immune-Induced Aplastic Anemia Mice
qing-zhao, SHI ; zhi-liang, XU ; hui, WANG ; zhong-yan, JIANG
Journal of Applied Clinical Pediatrics 1986;0(01):-
Objective To investigate the influence of angelica sinenisis injection on bone marrow histology and ultrastructure in immune-induced aplastic anemia(AA) mice.Methods Female Balb/c mice were divided into normal group,model group,therapy group and contrast group.All mice were killed by cutting neck on the 12 th day, ulnas and femur were taken out. The bone marrow histology section and ultrastructure of mice ulnas were observed. The quantities of hematopoietic cells were counted. The number of femur bone marrow mononucleate cells (MNC) were measured.Results The quantities of hematopoietic cells in model group were lower than those in normal group (P
6.Role of NRF2 signaling pathway in trichloromethane-induced oxidative stress in L02 cells
TAN Shi ying ZHONG Yuan fang QIU Yi bing ZOU Zhi hui YU ri an
China Occupational Medicine 2022;49(05):530-
Objective - ( )
To investigate the effects of nuclear factor erythroid 2 related factor 2 NRF2 on the oxidative stress
( ) Methods ) ,,
induced by trichloromethane TCM in human normal hepatocyte L02 cells. i L02 cells were stimulated with 1 2
, , , ( ),
4 8 12 16 and 20 mmol/L TCM solution dissolved in dimethyl sulfoxide and the control group and blank group were set
, - ,
up. After culturing for 24 hours the cell viability was detected by CCK 8 colorimetric method and the concentration of TCM
) -, -
stimulation was screened. ii L02 cells in logarithmic growth phase were randomly divided into control group and low medium
- , , ,
and high dose groups. After 24 hours of exposure to 0 4 8 and 12 mmol/L TCM the cells were collected. The activity of
( ), ( ), ( - ) ( )
superoxide dismutase SOD catalase CAT glutathione peroxidase GSH Px and the level of malondialdehyde MDA
NRF2, - (HO-1),
were detected by colorimetric analysis. The mRNA expression levels of heme oxygenase 1 glutamate cysteine
(GCLC) () (NQO1) -
ligase catalytic subunit and NAD P H quinone dehydrogenase 1 were detected by real time fluorescence
, - ,
polymerase chain reaction. The protein levels of NRF2 HO 1 GCLC and NQO1 were detected by Western blotting.Results ) , , , ,
i When the concentration of TCM was 4 8 12 16 and 20 mmol/L the survival rate of L02 cells decreased
( P ) , ,
significantly compared with the control group all <0.05 . The concentration of 0 4 8 and 12 mmol/L were selected as the
) , -
stimulation doses for subsequent experiments. ii Compared with the control group the activities of SOD and GSH Px in L02
( P ) ( P ), -
cells in the three doses groups decreased all <0.05 and the levels of MAD increased all <0.05 with a dose effect
- (P ),
relationship. The CAT activity of L02 cells in the medium dose group was lower than that in the control group <0.05 and the
- ( P )
CAT activity of L02 cells in the high dose group was lower than that in the others three groups all <0.05 . Compared with the
, NRF2 - (P ),NRF2
control group the relative expression levels of mRNA in L02 cells in the low dose group decreased <0.05
- (P ), NRF2
mRNA in L02 cells in the medium dose group increased <0.05 mRNA and NRF2 protein expression in L02 cells in
( P ) HO-1,GCLC, NQO1 ,
the highdose group increased both <0.05 . The relative expression level of mRNA and GCLC NQO1
( P )
protein expression in L02 cells in the three doses groups increased compared with the control group all <0.05 . The relative
NRF2 - - -
expression level of mRNA in L02 cells in the high dose group was higher than that in the low and medium dose groups
( P ), - (P ),
both <0.05 and the relative expression of NRF2 protein was higher than that in the low dose group <0.05 but the
HO-1 GCLC - - (
relative expression levels of and mRNA and HO 1 protein level were lower than those in the medium dose group all
P )Conclusion -
<0.05 . TCM exposure can inhibit the proliferation of L02 cells by inducing oxidative stress with a dose effect
,
relationship. In this process the antioxidant mechanism mediated by NRF2 was activated. The expression of antioxidant defense
, - ,
and detoxification related target genes downstream of NRF2 signaling pathway was activated and the expression of HO 1
-
GCLC and NQO1 was up regulated to alleviate the oxidative damage caused by TCM.
7.A study of kinematic parameters of normal youth in gait analysis
Zhong-wu GUO ; Guang-zhi WANG ; Hui DING ; Jing GAO ; Haishu DING
Chinese Journal of Rehabilitation Theory and Practice 2002;8(9):532-533
ObjectiveTo study basic pattern of normal youth in gait analysis.Methods28 healthy young persons as experimental subjects were studied. The gait analysis system based on digital video and digital image processing was employed to obtain kinematic parameters.ResultsThe means and standard deviations of kinematic parameters of normal youth were obtained. The differences of gait patterns between males and females were compared. The correlations between gait parameters and height, weight were analyzed respectively.Conclusions It is recommended that the values of the gait parameters and the trends obtained can be used as a standard gait pattern of normal youth. Statistically significant differences exist between the males and the females for most of the gait parameters. Furthermore, the differences of the values of gait parameters between the males and the females are not led only by the difference of height except very few parameters.
8.Study on serological blood group conversion rule and clinical blood transfusion in allogeneic hematopoietic stem cell transplantation.
Zhong-qing YU ; Zhi-feng GAO ; Hui-yu LI
Chinese Journal of Hematology 2012;33(8):637-641
OBJECTIVETo explore the conversion rule of serological blood group and blood group substance after successful allogeneic hematopoietic stem cell transplantation, and to provide theory for clinical special blood type identification and blood transfusion.
METHODSThe growth cycle of recipient WBC and RBC, RBC chimera, blood group antibody production and remaining in full transition were observed. Conversion rule of blood group substance, contradiction between cells typing and sera typing were detected by saline medium tube method and microcolumn gel method after stem cells transplantation.
RESULTSThe average time of engraftment in 21 recipients was about 18.6 days, RBC growth cycle in 8 major blood type incompatibility was 56.6 days, 25.9 days in 9 minor blood type incompatibility, 67 days in 4 bidirectional blood type incompatibility (P < 0.01). The ratio of RBC chimeric growth was 1:9, gradually converse to donor's blood group. Residue of recipient anti-A(B) was left after conditioning regimen, disappeared after full transformation, and recipient anti-A(B) was converse to donor's blood type in major blood type incompatibility. 5 A blood type recipient donated by O blood type blood generated anti-B instead of anti-A, 3 B blood type recipient generated only anti-A instead of B in minor blood type incompatibility, and 1 AB blood type recipient donated by A did not generate anti-B. Among 4 bidirectional blood type incompatibility, 2 B blood type recipient donated by A blood type blood did not generate anti-B, 2 A recipient by B could not produce anti-A. Recipient blood group substance helped original ABO blood type substance remain unchanged.
CONCLUSIONAmong patient with allogeneic hematopoietic stem cell transplantation, recipient's ABO and RBC blood type can be converse to donor's, but there is significant difference between patients of serological blood group and of normal people (P < 0.01). Recipient blood group substance helps original ABO blood type substance remain unchanged (P > 0.01).
Adult ; Blood Donors ; Blood Group Antigens ; immunology ; Blood Group Incompatibility ; immunology ; Blood Grouping and Crossmatching ; Blood Transfusion ; Female ; Hematopoietic Stem Cell Transplantation ; methods ; Humans ; Male ; Middle Aged ; Transplantation, Homologous ; immunology ; Young Adult
9.Disseminated herpes zoster in immunocompetent patients not due to varicella-zoster virus gene mutation.
Zhong-hui SUN ; Yun-yi GUO ; Ming LI ; Zhi-rong YAO
Chinese Medical Journal 2013;126(16):3193-3193
Adult
;
Herpes Zoster
;
etiology
;
Herpesvirus 3, Human
;
genetics
;
Humans
;
Male
;
Middle Aged
;
Mutation
10.The identification and sequence analysis of ALV-J isolated from layers.
Chinese Journal of Virology 2008;24(5):369-375
Two Avian leukosis viruses of subgroup J (ALV-J) were isolated from layers by inoculating the sample into chicken embryo fibroblast (CEF) cells and by indirect fluorescent assay (IFA) with ALV-J specific monoclonal antibody JE-9. Sequence comparison indicated the gp85 identities were only in the ranges of 83.4%-87.3% compared with five international reference strains and 86.4%-89.6% compared with eight Chinese strains isolated from white meat-type chickens. The gp37 identities were in the range of 91.8-96.4% compared with the five international strains and 93.4-95.9% compared with the eight domestic strains. When compared with the above thirteen strains, two layers isolates were more close to the prototype HPRS-103 and had less deletion in 3'-Ter than those strains. All strains isolated from white meat-type chickens in China had a deletion in the "E" region of 3'-Ter except these two isolates, suggesting these two ALV-J isolates from layers have different evolution origins from other Chinese isolates from white meat-type chickens.
Animals
;
Avian Leukosis Virus
;
classification
;
isolation & purification
;
Base Sequence
;
Chick Embryo
;
DNA, Viral
;
chemistry
;
Molecular Sequence Data
;
Phylogeny