Adult ; Atropine ; therapeutic use ; Bronchodilator Agents ; therapeutic use ; Combined Modality Therapy ; Female ; Hemofiltration ; Humans ; Insecticides ; poisoning ; Male ; Middle Aged ; Organophosphorus Compounds ; Poisoning ; therapy ; Treatment Outcome

OBJECTIVETo investigate the effects of FTY720, a new immunosuppressive agent, on apoptosis and autophagy in multiple myeloma(MM) cell line U266 and to clarify its molecular mechanism.

METHODSU266 cells were treated with 0, 2.5, 5.0, 10.0 and 20.0 µmol/L FTY720 for 24 hours, and the cell viability was assayed by CCK-8 method. Then U266 cells were treated with 20.0 µmol/L FTY720 for 0, 2, 6 and 24 hours, the cell viability was tested. The apoptotic rates induced by different doses and time points of FTY720 were tested by flow cytometry separately. The expression of LC3B was detected by Western blot after U266 cells treated with different doses of FTY720 to see autophagy. U266 cells were treated with FTY720 ± Bafilomycin A1, an inhibitor of autophagy, for 24 hours, then the cell viability and apoptotic rates were tested. Meanwhile the expression of survivin, anti-apoptotic factors, were tested by Western blot.

RESULTSThe cell viability and the apoptotic rates were inhibited significantly by FTY720 (P < 0.05) in time-dependent and dose-dependent manner. The expression of LC3B-II increased significantly in a dose-dependent manner, it indicated that the autophagy was induced by FTY720. Bafilomycin A1 could rescue the cell viability and apoptotic rates in U266 cells treated with FTY720, and it could also rescue the expression of survivin decreased by FTY720.

CONCLUSIONSFTY720 can cause apoptosis and autophagy of U266 cells. The autophagy promote the apoptosis, which maybe due to the degradation of anti-apoptotic factors such as survivin or their upstream factors in lysosomes through autophagy.

Apoptosis ; drug effects ; Autophagy ; drug effects ; Cell Line, Tumor ; Fingolimod Hydrochloride ; Humans ; Multiple Myeloma ; pathology ; Propylene Glycols ; pharmacology ; Sphingosine ; analogs & derivatives ; pharmacology

Objective To investigate the regulatory effects of fenofibrate on TNF-α-induced CD40 expression and matrix metalloproteinase (MMP) activity in human vascular endothelial cells (HUVECs). Methods Quantitative RT-PCR and flow cytometry were employed to evaluate the effect of fenofibrate on TNF-α-induced CD40 mRNA and cell surface CD40 expression in HUVECs, and gelatin zymography was used to determine the effect of fenofibrate on the gelatinolytic activities of MMP-2 and MMP-9 in TNF-α-stimulated HUVECs. Results Fenofibrate at the concentrations of5×10-5, 1×10-4 and 2×10-4mol/L significantly reduced TNF-α-induced increment of CD40 mRNA and cell surface CD40 expressions (P＜0.01), with the maximal inhibition achieved at the concentration of 1 × 10-4 mol/L. Fenofibrate at 2× 10-4 mol/L did not further decrease CD40expression induced by TNF-α. Fenofibrate significantly inhibited the stimulatory effect of TNF-α on MMP-2 and MMP-9 activities in HUVECs. Conclusion Fenofibrate reduces TNF-α-induced increment of CD40 expression and MMP-2 and MMP-9 activities in HUVECs.

OBJECTIVETo explore the mechanism of acupuncture in delaying aging.

METHODSUsing SAMP10 mice and normal control SAMR1 as model and applying RT-PCR and DIG probed Northern blot techniques to observe expression of NF-E2, YB-1, LRG47 genes in whole brain, cortex and hippocampus in the 8-month SAMR1 control group, 8-month SAMP10 control group, 8-month SAMP10 acupuncture group and 8-month SAMP10 non-point acupuncture group.

RESULTSIn the SAMP10 control group, the expression of NF-E2, YB-1 and LRG47 were down-regulated in the whole brain, cortex and hippocampus, and after acupuncture they were up-regulated and tended to normal.

CONCLUSIONAging of the SAMP10 mouse brain is related with expression of NF-E2, YB-1 and LRG47 genes, and acupuncture can regulate the expression of NF-E2, YB-1 and LRG47 genes, improving the functions of erythrocyte series, increasing proliferation of cells and immune function of cells in anti-bacteria, hence anti-aging.

Acupuncture Therapy ; Aging ; metabolism ; Animals ; Brain ; metabolism ; Female ; GTP-Binding Proteins ; genetics ; Gene Expression Regulation ; Male ; Mice ; NF-E2 Transcription Factor, p45 Subunit ; genetics ; RNA, Messenger ; analysis ; Y-Box-Binding Protein 1 ; genetics

OBJECTIVETo probe the mechanism of acupuncture for anti-aging.

METHODSIn the senescence accelerated mouse the SAMP10 and the SAMR1, by using RT-PCR and DIG-labeled Northern blot technique, the expression differences of HSP84 and HSP86 genes in whole brain, cortex and hippocampus in the 4 groups,8-month SAMR1 control group, 8-month SAMP10 control group, 8-month SAMP10 acupuncture group and 8-month SAMP10 non-point acupuncture group were investigated.

RESULTSIn the SAMP10 control group, the expression of HSP84 and HSP86 were down-regulated in the whole brain, the cortex and the hippocampus, and they were up-regulated after acupuncture, tending to the normal group.

CONCLUSIONBrain aging of the SAMP10 mouse is related with abnormal expression of HSP84 and HSP86 genes, and acupuncture can strengthen the protection of cells, inhibit apoptosis and anti-oxidative stress through regulating expression of HSP84 and HSP86, hence anti-aging.

Acupuncture Therapy ; Aging ; metabolism ; Animals ; Blotting, Northern ; Brain ; metabolism ; Cerebral Cortex ; metabolism ; Female ; HSP90 Heat-Shock Proteins ; genetics ; Hippocampus ; metabolism ; Male ; Mice ; RNA, Messenger ; analysis

Objective To analyze the inherent quality of non-cited papers published in Chinese Journal of Endemiology, so as to identify the direction of invitation for contributions, and to provide the evidence for improving the academic quality and the cited rates. Methods Scientific papers published in Chinese Journal of Endemiology from 2004 to 2006, with zero cited rates were retrieved in China National Knowledge Infrastructure by March 24, 2011. These articles were statistically analyzed according to publication year, section type, download frequency, etc. Results A total of 200 papers were not cited, accounting for 23.04% (200/868) of the total number of papers published in the journal in the three years. Respectively, 17.23% (46/267), 24.39% (70/287)and 26.75% (84/314) of the papers published in 2004, 2005 and 2006 did not receive a single citation. The number of non-cited papers in editorial and expert forum column was zero, all articles in those column had been cited;followed by review column, non-cited rate was 6.98% (3/43);articles published in the column of short reports were seldom cited and non-cited rate was the highest of 54.02%( 121/224);all the columns of experimental study, field epidemiological investigation, clinical medicine, detection method and sanitary control had a certain percentage of non-cited papers. All of the 200 non-cited papers were downloaded, the download frequency ranged from 1 to 109, with an average of 27.21 times. Conclusions Adequate space should be given to the columns of editorial, expert forums, review, experimental study and field epidemiological investigation;the number of short reports should be reduced appropriately. The journal should enhance cited rate of published papers, comprehensively improve the academic quality of the articles, and contribute to the academic exchange and discipline development.

Objective To analysis the inherent quality of highly cited papers published in Chinese Journal of Endemiology, so as to identify the direction of invitation for contributions, find high quality articles, and to improve the journal's core competitiveness. Methods Scientific papers published in Chinese Journal of Endemiology from 2000 to 2006, with citation rate equal to or higher than 20 times were retrieved in China National Knowledge Infrastructure(CNKI) by December 27, 2010. These articles were statistically analyzed according to publication year, section type, author, and geographical distribution of units. Results A total of 68 highly cited papers were obtained. The citation frequency of the highly cited papers ranged from 20 to 94, with an average of 31.09 times. The highly cited papers were published in 2000 at most, accounting for 25.0%(17/68); followed by 2001,accounting for 20.6% (14/68); at least in 2006, accounting for 2.9% (2/68). Of the highly cited papers, experimental study articles was in the highest proportion of 30.9%(21/68); followed by field epidemiological investigation articles,accounting for 23.5%(16/68); editorial, review articles accounting for 10.3%(7/68) and 8.8%(6/68), respectively;short reports, case reports, meeting records etc were not highly cited papers. The number of highly cited papers in editorial, expert forums, academic contend accounted for higher proportion of total number in corresponding section types(7/19, 3/11, 3/7). Highly cited papers came from 13 provinces(municipalities), there were 10 authors contributed two or more highly cited papers, and 8 units contributed two or more highly cited papers. Conclusions Adequate space should be given to experimental research, field epidemiological investigation, editorial, expert forums andacademic contend articles due to their high rate of citation. More attention should be paid to further consolidate and expand excellent authors group, and to intensify the invitation for key issues from influential experts.

Aim To establish a new model of skin damage by u-sing vincristine to transgenic zebrafish (krt4:NTR-hKikGR).Methods Skin fluorescent transgenic zebrafish embryos after 24 h fertilization were treated with the 0.01~0.04 mmol·L-1 vincristine,and zebrafish skin cell ablation was investigated un-der fluorescence microscope after 24 h,at same time skin death cells were detected with TUNEL assay and image processed, then the protein expressions of KRT4, caspase-3 and p53 were assessed with Western blot. Results 0.02 mmol·L-1and 0.04 mmol·L-1vincristine could obviously induce zebrafish skin cell apoptosis(P<0.01) with statistically significant differ-ence compared with the control, and the same result could be accomplished in TUNEL assay. Results of Western bolt showed that vincristine could increase the embryos caspase-3 and p53 expression(P <0.01), while vincristine in high concentration might decrease KRT4 markedly(P<0.01). Conclusion Vin-cristine can induce damage on zebrafish skin with suppression KTR4,which can be used as a new skin damage model.

Aim To investigate the protective effect of Qi ZhiXiaoke granules ( QZXK ) on nerve injury using zebrafish and nerve cell injury models. Methods The nerve injury model was established using wild zebrafish AB line, 72 hours after fertilization treated with 1-methyl-4-phenyl-1 , 2 , 3 , 6-four pyridine ( MPTP ) .Then QZXK of different doses were administered for three days,and the trajectory of the zebrafish behavior was recorded and analyzed. Neuroblastoma PC12 cells were incubated with different concentrations of QZXK and MPTP,and the cell viability of PC12 cells was de-tected by MTT. The mitochondrial membrane potential and expression of apoptosis related protein Caspase3 were measured by kits. Results Compared with con-trol group,MPTP reduced the movement distance of ze-brafish,and with the increase of concentration, QZXK promoted the movement distance and reversed the swimming behavior abnormality of zebrafish. Compared with control group, QZXK could inhibit the apoptosis induced by MPTP and promote the cell viability of PC12 cells with MPTP. QZXK improved the membranepotential and decreased the expression of Caspase3 . Conclusions QZXK exerts neuroprotective effect in the process of nerve injury induced by MPTP. The mechanism may be related with inhibiting apoptosis of neural cells. These experiment provides experimental and theoretical foundation for QZXK promoting cogni-tive function.

This study was purpose to investigate the role of reactive oxygen species (ROS) in apoptosis and autophagy induced by FTY720 in multiple myeloma cell line U266. U266 cells were treated by different concentrations of FTY720 for 24 h, the apoptotic rates were detected by flow cytometry, and the expression of LC3B was detected by Western blot. The results indicated that apoptosis and autophagy were induced by FTY720 in U266 cells. Autophagy induced by FTY720 could lead to cell death. Bafilomycin A1, the inhibitor of autophagy, could enhance the cell viability in U266 cells treated with FTY720. NAC or Tiron, ROS scavenger, could decrease the FTY720 induced apoptosis and the expression of LC3B-II was reduced in combination of FTY720 with NAC or Tiron as compared with treatment with FTY720 only. It is concluded that FTY720 can induce U266 cell apoptosis and autophagy. ROS is the mediator that regulates both the apoptosis and autophagy in multiple myeloma cells.
1,2-Dihydroxybenzene-3,5-Disulfonic Acid Disodium Salt ; Apoptosis ; drug effects ; Autophagy ; drug effects ; Cell Line, Tumor ; Fingolimod Hydrochloride ; Humans ; Macrolides ; Microtubule-Associated Proteins ; metabolism ; Multiple Myeloma ; metabolism ; pathology ; Propylene Glycols ; pharmacology ; Reactive Oxygen Species ; metabolism ; Sphingosine ; analogs & derivatives ; pharmacology