2.Influence of Erythropoietin and Inflammatory Cytokines on Pathogenesis of Cerebral Palsy
Weiyuan TAO ; Fang WEN ; Hanyun YAO ; Yang SUN
Chinese Journal of Rehabilitation Theory and Practice 2008;14(1):62-64
Objective To investigate the effect of erythropoietin(EPO)as a brain-protective factor and inflammatory cytokines in the pathogenesis of cerebral palsy(CP).Methods Serum samples from 31 CP patients,37 neonates with CP risk factors such as hypoxic-ischemic injury and/or perinatal infection,and 20 controls of neonates or children were obtained respectively.EPO,tumor necrosis factor(TNF)-α and interleukin(IL)-6 levels were measured with the enzyme-linked immunosorbent assay double sandwich method(ABC-ELISA).Results The serum EPO level of neonatal patients was higher than that of controls or CP group(P<0.01),but there was no significant difference between CP group and controls.The serum TNF-α and IL-6 levels of CP and neonatal patients were higher than that in controls(P<0.01).The serum TNF-α level of CP group was higher than that of neonatal patients(P<0.05).There was no significant difference between CP group and neonatal patients in serum IL-6 level.Conclusion The inflammatory responses mediated by proinflammatory cytokines may play a role in the pathogenesis of cerebral palsy.
3.Studies on the metabonomics of rat liver injury induced by ethanol and interfering effects of Yin Chen Hao Tang
Xi-Jun WANG ; Lian LIU ; Hui SUN ; Wen-Jun SUN ; Hai-Tao LV ;
Chinese Pharmacological Bulletin 1986;0(04):-
Aim To determine potential biomarkers contributed to occurrence, development and recovery of ethanol-induced liver injury in rat and elucidate hepatoprotective effect of Yin Chen Hao Tang based on metabonomic investigation. Methods A UPLC-Q-TOF/MS based metabonomic method was developed for investigating trajectory change and inter-relationship of urinary metabolome of rats with different treatments. Results Four potential biomarkers were determined which contributed to occurrence, development and recovery of ethanol-induced liver injury in rat, and Yin Chen Hao Tang could significantly recover trajectory change in disorder. Conclusion The developed method was successfully applied to investigate ethanol-induced liver injury in rat, and also hepatoprotective effect of Yin Chen Hao Tang was elucidated.
4.Protective effects of Salvia miltiorrhiza on rats with streptozotocin diabetes and its mechanism
Gang LIU ; Guangju GUAN ; Tonggang QI ; Yuqin FU ; Xuegang LI ; Yun SUN ; Tao WU ; Rongzhu WEN
Journal of Integrative Medicine 2005;3(6):459-62
OBJECTIVE: To explore the effects of Salvia miltiorrhiza on renal morphology and renal function of rats with streptozotocin diabetes. METHODS: Thirty male Wistar rats were randomly divided into three groups, which were normal control group, untreated group and Salvia miltiorrhiza-treated group. Diabetic nephropathy was induced in rats of the last two groups by intraperitoneal injection of streptozotocin after unilateral nephrectomy. Then the rats in the normal control and untreated groups were fed with normal saline while those in the Salvia miltiorrhiza-treated group were fed Salvia miltiorrhiza preparation for 8 weeks. The glomerular volume (VG), kidney-to-body weight ratio (KW/BW), urinary albumin excretion rate (UAER) and creatinine clearance (Ccr) were observed. The expression levels of transforming growth factor-beta1 (TGF-beta1), connective tissue growth factor (CTGF), fibronectin (FN) and plasminogen activator inhibitor-1 (PAI-1) were detected by real-time quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) at the end of the experiment. RESULTS: UAER, Ccr, VG and KW/BW ratio were significantly higher in the untreated group than those in the normal control group (P<0.05). The expression levels of TGF-beta1, CTGF, PAI-1 and FN in the untreated group were also significantly higher as compared with those in the normal control group (P<0.05). UAER, Ccr, VG, KW/BW ratio and the levels of TGF-beta1, CTGF, PAI-1 and FN in the Salvia miltiorrhiza-treated group were obviously lower than those in the untreated group (P<0.05). CONCLUSION: Salvia miltiorrhiza can protect rats with streptozotocin diabetes from diabetic nephropathy by suppressing the over-expressions of TGF-beta1, CTGF, PAI-1 and FN in renal cortex.
5.Cholesterol ester transfer protein regulates the hepatic SR-B1 mRNA expression in mice
Wen GUO ; Tao YANG ; Zhenzhen FU ; Yan SUN ; Xiaohui ZHU ; Beibei GAO ; Hongwen ZHOU
Chinese Journal of Endocrinology and Metabolism 2013;(3):259-260
The effect of cholesterol ester transfer protein(CETP) on SR-B1 mRNA expression in mouse liver was investigated.The results demonstrated that CETP transgenic mice showed lower serum total cholesterol and high density lipoprotein-cholesterol levels but higher total cholesterol and cholesterol ester content in liver when compared with wild type mice(P<0.05).The expression of SR-B1 mRNA in liver of CETP transgenic mice was significantly lower as compared with the control group(P<0.05).
6.Study on the inhibitive effect of mesenchymal stem cells on the immunological rejection in rats after liver transplantation
Zhenqiang SUN ; Weizheng JI ; Tao LI ; Jinming ZHAO ; Yongxing BAO ; Jinhui ZHANG ; Wensheng YANG ; Hao WEN
Chinese Journal of Digestive Surgery 2009;8(6):449-452
Objective To investigate the inhibitive effect of mesenchymal stem cells (MSCs) on the immunological rejection in rats after liver transplantation. Methods The recipients and donors were female SD rats and Wistar rats. All rats were randomly divided into 3 groups (28 rats in each group). Rats in group A were infused with normal saline; rats in group B received FK506 (0.25 mg/kg) every 2 days for 2 weeks after liver transplantation; rats in group C were injected with MSCs from male Wistar rats during liver transplantation. The pathological changes, expression of TGF-β1 and IL-10, Y chromosome location, changes of liver function and the survival of the recipients were detected on postoperative day 10. The levels of ALT and AST were analyzed by com-pletely randomised design analysis of variance, and the difference among the 3 groups were analyzed by LSD. Ridit was used to analyze the pathological grading. The survival was analyzed by Log-rank test after the Kaplan-Meier survival curve was drawn. Results The values of ALT and AST were (756±104)U/L and (635±134)U/L in group A, (197±49)U/L and (331±78) U/L in group B, (103±31)U/L and (150±38) U/L in group C, respectively. The difference in the level of ALT and AST among the 3 groups had statistical significance (F = 158, 265, P < 0.05). The liver function of rats in group B and C was better than those in group A (P < 0.01), and the liver function of rats in group C was better than those in group B. The mean values of ridit in group A, B and C were 0.8333, 0.4583 and 0.2083, respectively. The expression rates of TCG-β1 in group A, B and C were 18%±5% , 69%±20% and 85%±24% , with statistical difference among the 3 groups (F=191, P <0.01). There was a significant difference in IL-10 expression among group A (21%±5%), group B (75%±14%) and group C (91%±21%) (F=672, P<0.01). The TCG-β1 and IL-10 had strong positive expression in group B and C, and the expression of TCG-β1 and IL-10 was much stronger in group C than in group B; while the expres-sion of TCG-β1 and IL-10 was weak positive in group A. MSCs cells with Y chromosome were positively stained and were concentrated at the portal area in group C. The 50-day survival rate of rats in group A, B and C were 0, 10% and 90% , respectviely, with significant difference (χ~2=36, P < 0.01). The median survival time of rats in group C was 63 days, which was longer than that in group A and B. Conclusion Simultaneous injection of MSCs from donors during liver transplantation can inhibite the immunological rejection of recipients to the liver graft.
8.Expression analyses of BcUGT3 and BcUGT6, and their in vitro expression in Escherichia coli.
Yun-Wen TAO ; Jie-Sen XU ; Jing SUN ; Jian-He WEI ; Juan LIU ; Chun SUI
China Journal of Chinese Materia Medica 2014;39(2):185-191
The tissue-specific and MeJA-induced transcriptional levels of BcUGT3 and BcUGT6 in Bupleurum chinense were analyzed in the present study. The transcriptional levels of BcUGT3 in root, leaf, flower and fruit were similar and they all were higher than those in stem. The transcriptional level of BcUGT6 was the highest in leaf and the lowest in flower among in all tested tissues. With non-treated adventitious roots as control, BcUGT6's transcriptional levels were elevated to nearly 2 folds for 2 h, 8 h, 24 h, 2 d and 4 d in MeJA-treated adventitious roots of B. chinense. It showed that the transcriptional level of BcUGT6 was slightly affected by MeJA. While, BcUGT3's transcriptional levels were gradually elevated, and till 4 d after MeJA treatment, the expression level was about 7 folds than that of non-treated control. Using pET-28a (+), the expressions of two genes was investigated. Induced by IPTG, the target proteins were expressed in E. coli and then purified. All the results obtained in the present study will be helpful for follow-up bio-function analysis of BcUGT3 and BcUGT6.
Acetates
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pharmacology
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Bupleurum
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cytology
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enzymology
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genetics
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Cell Membrane
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metabolism
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Cyclopentanes
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pharmacology
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Escherichia coli
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genetics
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Gene Expression
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Gene Expression Regulation, Plant
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drug effects
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Hexosyltransferases
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chemistry
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genetics
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isolation & purification
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metabolism
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Intracellular Space
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metabolism
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Oxylipins
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pharmacology
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Protein Sorting Signals
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Protein Structure, Secondary
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Protein Transport
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Sequence Analysis
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Transcription, Genetic
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drug effects
10.The effect of brain-derived neurotrophic factor on the angiogenesis.
Chun-yan SUN ; Yu HU ; Tao WU ; Ya-dan WANG ; Hua-fang WANG ; Wen-juan HE
Chinese Journal of Pathology 2006;35(4):238-239
Animals
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Brain-Derived Neurotrophic Factor
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pharmacology
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Cell Movement
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drug effects
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Cell Proliferation
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drug effects
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Cells, Cultured
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Chick Embryo
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Chorioallantoic Membrane
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blood supply
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Endothelial Cells
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cytology
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drug effects
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physiology
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Female
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Humans
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Mice
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Mice, Inbred C57BL
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Neovascularization, Physiologic
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drug effects
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Vascular Endothelial Growth Factor A
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pharmacology