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Welcome to Chinese Journal of Clinical Pharmacology and Therapeutics,Today is Chinese

Table of Content

    Volume 17 Issue 1
    26 January 2012
    Effects of lipoxygenase inhibitor on proliferation of HepG2 cell line and MEK/ERK signaling pathway
    XIONG Qi-ru, XIA Jun, LI Li-xiang, QIAN Ye-ben, YU Hong-zhu, XU Ye-chuan
    2012, 17(1):  1-5. 
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    AIM: To investigate the effects of lipoxygenase inhibitor, on proliferation in hepatocellular carcinoma cell line HepG2 and MEK/ERK signaling pathway in vitro.METHODS: Different concentrations of nordihydroguaiaretic acid (NDGA) were used to treat HepG2 cell. The proliferation inhibition was analysed by alive cell count, MTT assay, the mRNA expression intensity of MEK1, MEK2, ERK1, ERK2 were examined by RT-PCR.RESULTS: NDGA can inhibit HepG2 cell proliferation viability in the dose-dependent manner. The mRNA expression intensity of MEK1, MEK2, ERK1, ERK2 showed a trend of decreasing while the concentrations of nordihydroguaiaretic acid increased. The mRNA expression intensity of MEK1 was significantly decreased than the control at any concentrations (P<0.05), meanwhile the mRNA expression intensity of MEK2, ERK1, ERK2 was significantly decreased than the control at concentrations of 100 μmol/L or 200 μmol/L (P<0.05).CONCLUSION: NDGA can inhibit proliferation of HepG2 cell line, the mechanism of which may be due to down-regulating MEK/ERK signaling pathway.
    Hydralazine reverses human gastric cancer cell lines p16 methylation and reactivates its expression
    ZHAO Jun, XIA Ya-bin, ZHANG Yi-sheng, ZHAO Guo-hai
    2012, 17(1):  5-9. 
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    AIM: To investigate the mechanism of p16 gene silencing and evaluate the effects of Hydralazine on gastric cancer cell lines in vitro.METHODS: Experimental group BGC-823 cells were treated with 10, 30, 100 μmol/L Hydralazine and control group cells were not treated. After 96 h, methylation specific PCR was used to detect the CpG island methylation state of p16 gene. The expression of p16 gene mRNA and protein were analyzed by RT-PCR and Western blot. BGC-823 cells were treated with six different concentrations of Hydralazine(0, 3, 10, 30, 100, 300 μmol/L)for 72 h, and MTT assay was used to observe the change of proliferation activity.RESULTS: P16 gene promoter region was hypermethylation in control group. P16 mRNA and protein were expressed at a low level in control group. In Hydralazine-treated group, p16 promoter region exhibited a demethylation state, and its mRNA and protein were expressed up-regulation.CONCLUSION: Promoter region hypermethylation is an important mechanism of p16 silencing. Hydralazine, an effective inhibitor of p16 methylation, can inhibit cell growth in human gastric cancer in vitro and be potentially used for the clinical treatment of human gastric cancer.
    Effects of silybin on inhibiting glycoxidative stress and improving the learning and memory in aging rats treated by D-galactose
    FU Yong-jin, PAN Jing-qiang, ZHANG Xiao-mu, KUANG Shao-shong
    2012, 17(1):  10-14. 
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    AIM: To investigate the effects of silybin on the glycoxidative stress and the abilities of learning and memory in aging rats induced by D-galactose.METHODS: The aging rats induced by D-galactose, the abilities of learning and memory were measured by Morris water maze test in rats.To assess the glycoxidative stress, the glycosylated hemoglobin(HbA1c) and fructosamine (FRA), advanced glycation end products(AGEs) in plasma,the activity of aldose reductase(AR) in red blood cell (RBC) were used , the levels of malondialdehyde (MDA) and AGEs and ability of superoxide dismutase(SOD) in brain tissue were also acquired.RESULTS: Compared with the control group, Sily groups(150 mg/kg and 75 mg/kg ) obviously inhibited the activity of AR(P<0.01), reduced the levels of FRA, HbA1c and AGEs in rats treated by D-galactose(P<0.01 or P<0.05), and the levels of MDA and AGEs were reduced while the activity of SOD in brain were elevated(P<0.01).CONCLUSION: Silybin could improve the abilities of learning and memory in rats treated by D-galactose, and it might be related to the inhibition of glycoxidative stress and ability of AR.
    Effects of diammonium glycyrrhizinate phosphatidylcholine complex treatment on rat nonalcoholic fatty liver disease
    CHENG Yong, YU Feng
    2012, 17(1):  15-19. 
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    AIM: To observe the therapeutically effect of diammonium glycyrrhizinate phosphatidylcholine complex (DGLL) on the non alcoholic fatty liver disease (NAFLD).METHODS: NAFLD rat model was constructed by feeding rats with high fatty and cholesterol diet for 8 weeks. And NAFLD model was subdivided into 6 subgroups: control group, model group, polygene phosphatidylcholine capsules group and DGLL groups (100,300,900 mg/kg). At the end of 12 week, all rats were killed to detect the blood lipids, oxidative stress, liver function, insulin-related and the pathological changes.RESULTS: DGLL could significantly reduce the NAFLD rats aminotransferase (ALT, AST) activity, malondialdehyde (MDA) content, TNF-α level, fasting blood glucose (FBG), fasting insulin (FINS) level and fasting insulin resistance index(HOMA-IR). DGLL could also increase superoxide dismutase (SOD) activity and improve NAFLD rats total cholesterol (TC) and triglyceride (TG) levels.CONCLUSION: DGLL can be used to treat NAFLD, and the mechanism may be related to lowering blood lipids and improving liver function, anti-oxidation and insulin resistance.
    Acute toxicity of protein C activator from venom of Agkistrodon halys in rats and mice
    DUAN Ting, ZHANG Gen-bao, ZHOU Bing
    2012, 17(1):  20-24. 
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    AIM: To investigate the acute toxicity of protein C activator from venom of Agkistrodon halys in rats and mice.METHODS: Rats using the up-and-down procedure and mice using median lethal dose; the acute toxical symptoms, signs, death time and accumulated death rate were observed.RESULTS: PCA tail intravenous of rats (dose of 17.5-175 mg/kg), mice (dose of 6.25-11 mg/kg) poisoning in different degree of mouth and nose foam bleeding, dyspnea, heart rate, unstable walking, crouching, consecutive convulsion. The LD50 and its 95%confident limit of PCA to rats and mice were 29.57 (17.5-55) mg/kg and 8.05 (7.55-8.54) mg/kg respectively. A massive hemorrhage was noted in double lung, and pathological examination shows hemorrhage mainly involved in the alveoli, bronchi, etc. Other organs showed no obvious abnormality.CONCLUSION: The main toxicity of PCA from venom of Agkistrodon halys was hemorrhage induced by anticoagulation. In addition, the acute respiratory failure induced by pneumorr- hagia was the major cause for animal death.
    Transmission functions of fusion protein CTP-HBcAg18-27-Tapasin in the cells
    LIU Hong-hong, CHEN Xiao-hua, ZHOU Li-qin, LIU Xue-ni, YU Yong-sheng, ZANG Guo-qing, TANG Zheng-hao
    2012, 17(1):  25-29. 
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    AIM: To observe the function of transduction of fusion protein CTP-HBcAg18-27-Tapasin in antigen presenting cells.METHODS: Bone marrow derived DCs isolated from BALB/c mice were cultured with recombinant granulocyte-macrophage colony-stimulating factor and recombinant interleutin-4 for 5 days followed by LPS added to induce DCs maturation. Then, different dosages of CTP-HBcAg18-27-Tapasin and RPMI-1640 were added to cell culture medium. Subsequently, the distribution and localization of intracellular immunofluorescence were observed by confocal microscopy with fluorescence intensity assaying quantitatively. Futhermore, the transduction efficiency of CTP-HBcAg18-27-Tapasin was evaluated by detecting the differences of expression of Tapasin using western blot in different group.RESULTS: DCs were cultured and identified successfully; Immunofluorescence confirmed the CTP-HBcAg18-27-Tapasin could penetrate the membrane into the cytoplasm of DCs but not into the nucleus. Fluorescence intensity of 50 μg/L CTP-HBcAg18-27-Tapasin group were higher than 10 μg/L CTP-HBcAg18-27-Tapasin group and blank groups. Western blot also confirmed that CTP-HBcAg18-27-Tapasin can penetrate the cell membrane into the DCs, and the data showed the difference was statistical.CONCLUSION: CTP-HBcAg18-27-Tapasin has the ability of penetrating and locating in the cytoplasm of DCs.
    Analysis on resistance of Acinetobacter Baumannii and the extended spectrum beta-lactamases and carbapenemases
    LI Xiao-ning, LI Juan, YAO Yong-hong
    2012, 17(1):  30-33. 
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    AIM: To analyze drug resistance of Acinetobacter Baumannii and detect the rate of extended spectrum beta-lactamases and carbapenemases which produced by Acinetobacter Baumannii in the hospital.METHODS: The disk diffusion method(K-B)for drug susceptibility testing was used, Clinical and Laboratory Standards Institute(CLSI) was taken for determing ESBL,the carbapenemases was modified by Hodge test.RESULTS: The susceptibility test to antibioties showed the resistance rates were 72.6% to Imipenem and Meropenem, 61.5%-100% to 10 antibioties including Amikacin and Cefotaxime, 34.8% to Cefoperazone/Sulbactam, 54.1% to Levofloxacin. In 135 strains, there were 22 produced ESBL(16.3%), 46 produced carbapenemases(34.1%).CONCLUSION: The drug resistance rate of Acinetobacter Baumannii is high in the hospital, it should be intensified in bacterium detection and drug susceptibility test to guide clinical drug usage more reasonability. Cefoperazone/Sulbactam will be advised as clinical experience of medication. The resistance to beta-lactam in Acinetobacter Baumannii is possibly related to ESBL and carbapenemases.
    Effect of extracellular acidification on the proliferation, apoptosis and Cathepsin K mRNA of rat articular chondrocytes in vitro
    RONG Chao, CHEN Fei-hu, JIANG Sheng, HU Wei, ZHANG Cheng-cheng, WU Fan-rong
    2012, 17(1):  34-39. 
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    AIM: To investigate the effects of various extracellular solutions on rat chondrocytes proliferation and apoptosis in vitro, and relation of Cathepsin K mRNA expression and extracellular acidosis.METHODS: Articular chondrocytes were obtained from rats using type II collagenase digestion method. The chondrocytes were divided into four groups and incubated in different pH extracelluar solution (pH 7.4, pH6.5, pH6.0, pH5.5) for three hours. MTT assay was employed to determine the proliferation of articular chondrocytes in acidic solutions. Effects of extracellular acidosis on chondrocyte apoptosis were observed by Hoechst 33258 and Annexin V/PI staining. The expression of Cathepsin K mRNA were detected by real time reverse transcription PCR.RESULTS: Proliferation of articular chondrocytes were inhibited observably by acidosis (P<0.05). Apoptosis rate of articular chondrocytes were increased comparing with control group (P<0.05). The expression of Cathepsin K mRNA level gradually increased following the degree of acidity in extracellular solution.CONCLUSION: Extracellular acidosis can restrain the proliferation and promote the apoptosis of articular chondrocytes in vitro, and increase the expression of Cathepsin K mRNA. It has provided an experimental evidence on mechanism bone destruction in Rheumatoid arthritis.
    Artesunate enhance the ability of peritoneal macrophages endocytosing LPS and Escherichia coli and its mechnisms
    YU Meng-chen, PAN Xi-chun, LI Xiao-li, LI Jun, XIAO Kang-kang, LI Bin, ZHOU Hong
    2012, 17(1):  40-46. 
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    AIM: To investigate the effect of artesunate (AS) on peritoneal macrophages endocytosing lipopolysaccharide/endotoxin (LPS) and phagocytosing Escherichia coli.METHODS: Effects of various concentrations of monodansylcadaverine (MDC) and chloroquine(CQ) on the viability of peritoneal macrophages were observed by MTT test. Effects of artesunate, monodansylcadaverine and chloroquine on LPS internalization of peritoneal macrophages were detected by confocal laser scaning microscopy. The effect of artesunate on Escherichia coli internalization of peritoneal macrophages was examined by confocal laser scaning microscopy and bacterial clone forming counting test. The effect of artesunate on class A scavenger receptor (SR-A) mRNA expression was measured using RT-PCR method.RESULTS: 25 μg /mL of MDC and 20 μg /mL of chloroquine had no effect on the viability of peritoneal macrophages. Artesunate could increase LPS internalization of peritoneal macrophages, while MDC and chloroquine could inhibit LPS but artesunate could still increase LPS internalization of macrophages treated with MDC and chloroquine. Artesunate could increase Escherichia coli internalization, and artesunate could up-regulate SR-A mRNA expression of peritoneal macrophages treated with or without LPS.CONCLUSION: Artesunate could enhance the ability of the peritoneal macrophages to internalize LPS and Escherichia coli, which was associated with up-regulation of SR-A mRNA expression of the peritoneal macrophages.
    Mechanisms of lumiracoxib on apoptosis in human lung cancer cells
    HAO Ji-qing, SUN Gen-yun, SHEN Yu-xian
    2012, 17(1):  47-51. 
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    AIM: To investigate the possible mechanism of Lumiracoxib (LUM)on the apoptosis of lung cancer cells.METHODS: Cells growing to confluence were treated with IL-1β (1 μg/L) prior to stimulation with LUM(0,15,30,60 μmol/L)for 24 hours. Western blot analysis was used to examine the level of ERK2, p-ERK and Bcl-2 protein in human NSCLC cell lines. Western blot analysis was used to examine the expression of Bcl-2 and Bax in A549 and NCI-H460 cells after exposed to various concentrations of LUM.RESULTS: LUM inhibited the up-regulated ERK2 and p-ERK as well as the down-regulated Bcl-2 expression in A549 and NCI-H460 cells. Additionally, LUM decreased the expression of Bcl-2 protein. And it increased the expression of Bax in A549 cells dependently on its doses. However, it had no effect on NCI-H460 cells. The ratio of Bcl-2/Bax decreased correspondingly.CONCLUSION: The mechanisms of the apoptotic effect of Lumiracoxib may be related to regulating Bcl-2 via ERK signal transduction pathway in human NSCLC cell lines.
    Effect observation of foam sclerotherapy of lauromacrogol combined with surgery for great saphenous varicose veins
    LU Wei-qin, JIANG Jin-song, YANG Guang-wei, LAI Ji-fu, LU Kai-ping
    2012, 17(1):  52-54. 
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    AIM: To evaluate the efficacy and safety of foam sclerotherapy of lauromacrogol combined with surgery for great saphenous varicose veins.METHODS: 86 patients with great saphenous varicose veins were randomized into 2 groups of A and B. Group A was treated by sapheno-femoral junction ligation and stripping of great saphenous veins. Verosis veins below the knee underwent foam sclerotherapy. Group B was treated by standard stripping of great saphenous veins.RESULTS: All treatments were completed as intended. The time of completing treatment and hospitalization were shorter in group A than those in group B(P<0.01). All patients were followed up 6 months with satisfactory outcomes except 3 patients in group A and 2 patients in group B with recurrence of varicose veins.CONCLUSION: Foam sclerotherapy of lauromacrogol combined with surgery for great saphenous varicose veins is safe and effective. Compared with traditional stripping operation, it has a shorter treatment and hospitalization time.
    Experience about causality assessment of fibrinogen in phase I clinical trial of Chinese herbal medicine
    LU Yan, LI Tao, JIA Zeng-qin, GAO Rui, TANG Xu-dong
    2012, 17(1):  55-58. 
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    AIM: To explore the fibrinogen evaluation problems and solution in phase I clinical trials.METHODS: Through a new phase I trial,there were 54 cases in phase I clinical trial volunteers' fibrinogen test, and analysised the results.RESULTS: Fibrinogen change did not exist consistency ,between 30 cases in single dose trial,there were 26 cases fibrinogen reduced ; In subsequent continuous drug trials to join the comfort drug group, the results of the two groups still did not exist consistency between groups, trial drug and placebo group fibrinogen appear consistency changes ,confirm the changes of fibrinogen is none of test drug.CONCLUSION: Fibrinogen test is affected by many kinds of factors, should be standardized operation process to reduce the influence; identify proper testing index range and inclusion criteria; can install placebo group if necessary, using a variety of means for causality assessment of the laboratory adverse events.
    Method of probability theory for calculating the absorption rate of drug in one-compartmental model
    LI Jin-wen
    2012, 17(1):  59-63. 
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    AIM: Based on probability theory, two concrete methods for absorption kinetics were proposed in one-compartmental model.METHODS: After an extravascular administration of drug, total resident time (Th) was regarded as sum of the resident time in site of administration (Tf) and the resident time in body (Tg). Not only are Tf and Tg independent each other, Tf, Tg and Th are nonnegative, continuous random variables also. According to convolution formula and characterization of one-compartmental model (exponential distribution), methods of probability theory for calculating the absorption rate of drug were obtained. These methods were composed of probability method (A approach) and numerical deconvolution method (B approach).RESULTS: The essential conditions of method of probability theory were in accordance with that of Wagner-Nelson (W-N) formula. The accuracy of A approach was identical with that of W-N formula. As long as the accurate value of first-order elimination rate constant (K) can be estimated, the accuracy of B approach was inferior to that of W-N formula. In case K value with relative error (±10%) was calculated, the accuracy of B approach was slightly superior to that of W-N formula.CONCLUSION: Method of probability theory can be suggested to estimate the percentage of drug absorbed and the concerned probability.
    Efficacy and safety of micafungin for the treatment of fungal infections: a Meta-analysis of seven randomized controlled study
    WU Jia-li, LIU Wen-hua, YIN Ping
    2012, 17(1):  64-68. 
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    AIM: To study the efficacy and safety of micafungin by Meta-analysis, providing a reference guide for the clinical use of antifungal agents.METHODS: The database was retrieved from Web of Science, EMBASE, Pubmed, the Cochrane Library, ClinicalTrials.Gov, Chinese Biomedical Literature Database, China Journal Full Text Database, and references of the included studies up to March 2011. Data were evaluated by RevMan 5.0 from the Cochrane Collaboration.RESULTS: Seven RCTS were included. The results of effectiveness evaluation showed that, the antibacterial effect of micafungin was superior to fluconazole (P=0.008) but had no statistically significant differences with lipid amphotericin B (P=0.38). There were no statistically significant differences between micafungin and control group in different types of Candida infection (P>0.05). The results of safety evaluation showed that there were no statistically significant differences between micafungin and fluconazole (P=0.40) or lipid amphotericin B (P=0.06) group in the incidence of adverse events. However, the incidence of infusion-related reactions in micafungin group were less than lipid amphotericin B group (P=0.001).CONCLUSION: Micafungin is a good alternative medication to lipid amphotericin B and fluconazole. There may be some publication bias in this study, so the results needs to be further confirmed by domestic research.
    Study on determining pharmacokinetics parameters of Shenfu injection by pharmacology effect method
    DU Ting, SUN Rong-jin, XU Guo-liang, LI Bing-tao, HUANG Li-ping, LI Jia
    2012, 17(1):  69-72. 
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    AIM: To determine pharmacokinetics parameters of Shenfu injection with pharmacodynamics effect.METHODS: Model of acute cardiogenic shock was made by ligating left coronary artery. Mean blood pressure (MBP) was as effective index. Dose-response curves were established with 1.25,2.5,5,10,20,25 mL/kg six doses and time-course effects were established with the 20 mL/kg dose. The time- stock of organisms curves were calculated with the time-course effects and dose-response curves. The pharmacokinetic parameters of Shenfu injection were analysed with DASver2.0 software.RESULTS: The main pharmacokinetics parameters were:t1/2=8.685 min, Ke=0.08 min-1, CL=1.417 L·min-1·kg-1, AUC(0-t)=12.63 mg·L-1·min-1.CONCLUSION: Apparent pharmacokinetic of Shenfu injection in rats fit one compartment
    Association of CYP3A5*3 with Acute Lymphoblastic Leukemia susceptiveness in Chinese Han children
    LIU Yan, LU Xiao-tong, SHENG Qi, TIAN Huai-ping, XU A-jing, TANG Yue-nian , BU Shu-hong, LI Li-xia, ZHANG Jian
    2012, 17(1):  73-77. 
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    To investigate the association of CYP3A5*3 with Acute Lymphoblastic Leukemia (ALL) susceptiveness in Chinese Han children.METHODS: CYP3A5 genotype was analyzed from 172 Chinese han children, including 52 ALL patients(27 female and 25 male) and 120 healthy controls(80 female and 92 male).Genomic DNA was extracted from blood sample, and PCR-RFLP was used to identify the polymorphism.RESULTS: This polymorphism were matched to Hardy-Weinberg equilibrium in all group.The allelic frequency of CYP3A5*3 was 0.721 (95% CI: 0.549, 0.893) in patients while 0.758 (95% CI: 0.674, 0.842) in healthy controls. There was no significant difference existed in CYP3A5*3 frequencies between patients and controls (P=0.275), males and females (P=0.432) in the total population.CONCLUSION: The CYP3A5*3 variant represents a common polymorphism in Chinese healthy children and ALL, and this polymorphism is poor association with ALL susceptiveness in children.
    Relationship between post-transplantation hypertension and dose, plasma concentration of tacrolimus
    XI Lan-yan YUAN Hong, CHENG Ke, ZHU Li-jun, YANG Guo-ping, ZHANG Gui-xiang, HUANG Zhi-jun
    2012, 17(1):  78-82. 
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    AIM: To investigate the incidence of hypertension after renal transplantation in patients administered with tacrolimus, and the correlation among blood pressure, tacrolimus dosage, plasma concentration and concentration/dose ratio of tacrolimus.METHODS: 200 renal transplant patients treated with tacrolimus were screened in the study, and the blood pressure were measured.Fifty-three hypertensive patients and Fifty-three normotensive patients were randomly enrolled from all screened patients.Tacrolimus was administrated at a stable dose for at least 3 days.Tacrolimus trough level was determined by Microparticle Enzyme Immunoassay (MEIA). The association of blood pressure in tacrolimus dosage and concentration were analyzed. Meanwhile, the dosage, plasmid level and concentration/dose ratio of tacrolimus were compared in the normotensive and hypertensive group.RESULTS: Hypertension was present in 104 post-transplantation patients out of 200 patients (52.0%). Spearman's correlation analysis revealed a positive correlation existed between systolic blood pressure (SBP) and the dose of tacrolimus (r=0.216, P<0.05). However, there was no significant correlation between diastolic blood pressure and tacrolimus trough level.The oral dosage of tacrolimus in hypertension group (3.11±1.49) mg/d was higher than that in normotensive group (2.42±1.07) mg/d (P<0.05). There was no significant difference in tacrolimus trough level between the two groups [HBP vs Nor: (7.76±3.86) ng/mL vs (7.56±2.67) ng/mL, P>0.05]. The concentration/dose ratio of tacrolimus was lower in hypertension group than that in normotensive group [(2.94±1.57) ng·d/mg·mL vs (3.95±3.02) ng·d/mg·mL, P<0.05).CONCLUSION: The present study demonstrated that SBP of renal transplant patients was positively correlated with tacrolimus daily dosage. Administration of tacrolimus with higher dosage may increase the predisposition to hypertension.
    Investigation and analysis on initial warfarin dosage and hemorrhagic risk factors for atrial fibrillation
    WEI Meng, TAO Yi-fu, YE Fei, XIE Du-jiang, ZHU Jun-rong, YU Feng
    2012, 17(1):  83-87. 
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    AIM: To compare the therapeutic efficacy and safety of two initial warfarin doses for atrial fibrillation(AF) and to further study the risk factors of hemorrhage.METHODS: A retrospective study was adopted. The inpatients with AF in recent 2 years were divided into two groups according to their initial warfarin doses: ultra-low dose group(1.25-1.875 mg) and low dose group (2.5-3.0 mg). The efficacy and safety of initial therapy of two groups were compared. Meanwhile, the major risk factors of bleeding were analyzed with logistic regression.RESULTS: There was no significant difference between two groups with respect to the safety (P>0.05).However, the mean time to reach a therapeutic INR was significantly longer in the ultra-low dose group than that of low dose group (P<0.05). In addition, the proportion of INR below the therapeutic range was much higher and the proportion of INR within the therapeutic range was much lower in ultra-low dose group than that of low dose group (P<0.001). Elderly (age>65 years), abnormal liver function, bleeding, stroke and amiodarone may increase the risk of hemorrhage significantly (OR>1,P<0.05).CONCLUSION: In the patients with AF, the ultra-low initial dosage has equal safety with regard to hemorrhage but increases the risk of thrombosis.At the same time,monitoring of the patients who combined amiodarone should be strengthened.
    Effects of Salbutamol on lung collapse during one-lung ventilation in patients with chronic obstructive pulmonary disease
    ZHOU Qi-fu, JIANG Zong- ming, WANG Hai-yong
    2012, 17(1):  88-91. 
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    AIM: To study the effects of Salbutamol aerosol inhalation prior to anesthesia induction on lung collapse during one lung ventilation in patients with chronic obstructive pulmonary disease.METHODS: Fourty patients with concomitant chronic obstructive pulmonary disease, scheduled for lobectomy were randomly allocated into observation group(n=20) and control group(n=20) . Salbutamol aerosol 200 μg (two puffs) were administered according to instructions before oxygenation via mask in observation group, whereas in control group no aerosol was given before oxygenation via mask. Anesthesia induction was initiated after 30 minutes' oxygenation in both groups. Extent of lung collapse was evaluated by verbal scale in 10 minutes and 20 minutes after one lung ventilation. Blood gas analysis was assayed in baseline, before anesthesia induction, double lung ventilation and 30 minutes during one lung ventilation(every 10 minutes was performed).RESULTS: There was statistical significance in lung collapse score between observation group and control group(P<0.05), the former was superior to the latter.Compared with the control group, the value of PaCO2 in anesthesia induction, double lung ventilation, 10 minutes and 20 minutes after one lung ventilation were lower than that in observation group, however , the value of PaO2 were higher in respective time.CONCLUSION: Salbutamol aerosol inhalation can accelerate lung collapse in early stage of one lung ventilation and at the same time provide better surgical access condition in patients with chronic obstructive pulmonary disease.
    Comparison of pregabalin and gabapentin on analgesic efficacy in patients after abdominal hysterectomy
    DAI Ping, HUANG Yan-li, LU Mo, CAI Dong-jiang, LI Zheng-yang
    2012, 17(1):  92-96. 
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    AIM: To investigate the analgesic efficacy and safety of pregabalin in patients after abdominal hysterectomy and compare with gabapentin.METHODS: A randomized, placebo-controlled study was conducted in 90 women undergoing abdominal hysterectomy who were anaesthetized in a standardized fashion. Patients received 300 mg pregabalin(Group P), 900 mg gabapentin(Group G) or placebo (Group C), 2 h prior to surgery, n=30 in each group. 100 mg flubiprofen axetil was intravenous infused at 4 h postoperation for conventional analgesia, rescue analgesia was administered at visual analog scales (VAS) scores >3 with intravenous tramadol. VAS scores at resting or coughing and sedation scores were recorded at arrived PACU, 1,2,4,6,8,12,18 and 24 h postoperation. The frequency and dosage of tramadol, incidence of adverse effects within 24 h postoperation were noted. The patients global satisfacation of postoperative analgesia was evaluated at 24 h postoperation.RESULTS: Recovery time from anesthesia was significantly longer in group P and G than that in group C(P<0.05). Resting VAS scores in 1,2 h and coughing VAS scores in 1,2 4 h postoperation were lower in group P than those in group C and G(P<0.05). Sedation scores in 1,2,6 h postoperation was significantly higher in group G than that in group C, and in 1,2 h postoperation were significantly higher in gourp P than those in gorup C(P<0.05). Time of patient's first request for analgesic was significantly longer in group P and G than that in group C(P<0.05). The number of tramadol rescue analgesia and dosage of tramadol were significantly less in group P and G than those in group C(P<0.05),and was significantly less in gorup P than that in group G(P<0.05). There was no significantly difference in incidence of dizziness in three groups, but the incidence of somnolence was significantly higher in group G than those in group C and P(P<0.05).The rate of patients, global satisfacation of postoperative analgesia which in “excellent” was significantly better in group P and G than that in group C (P<0.05), and also better in gorup P than that in group G(P<0.05).CONCLUSION: Pregabalin 300 mg given orally 2 h before abdominal hysterectomy can result in significantly reduced postoperative analgesic requirement and better patients global satisfacation compare with gabapentin 900 mg and placebo.
    Comparison of calsurf and curosurf on preterm infants respiratory distress syndrome
    DONG Yi-hui, YUAN Xian-wen, LI Peng
    2012, 17(1):  97-102. 
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    AIM: To evaluate and compare the efficacy and safety of pulmonary surfactant, calsurf and curosurf, on the treatment of preterm infant respiratory distress syndrome (RDS).METHODS: From January 2008 to August 2011,120 case of preterm infant RDS diagnosed and treated in the neonatal intensive care unit of our hospital were randomly devided into two groups, calsurf treatment group and curosurf treatment group, each including 60 cases, given calsurf and curosurf treatment though trachea cannula, respectively, observed the efficacy and complications.RESULTS: Both calsurf and curosurf had positive treatment effectiveness on RDS, represented for improvement the ventilator parameters, blood gas analysis results and RDS grade, respectively (P<0.05). The effects of curosurf was much better than calsurf especially for the duration of mechanical ventilation and oxygenization (P<0.05). There were no differences in complications of preterm infants between the two groups (P<0.05).CONCLUSION: Both calsurf and curosurf have positive effectiveness and good safety in the treatment of RDS, curosurf has efficacy advantage while calsurf has economic advantage.
    Effects of different doses of dexmedetomidine during induction anesthesia with sevoflurane inhalation
    MA Hua-xin, ZHOU Shao-li, XIE Han-bin, HEI Zi-qing
    2012, 17(1):  103-107. 
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    AIM: To evaluate the effects of two single preanesthetic doses of dexmedetomidine (0.5 μg/kg and 1.0 μg/kg) on bispectral index (BIS) and hemodynamic changes undergoing endotracheal intubation under induction anesthetic with sevoflurane inhalation.METHODS: In a double-blind and random study, 45 patients scheduled for gynaecologic laparoscopy operation were divided into 3 groups (n=15 for each). Patients in Group A were anesthetized with inhalation of sevoflurance; Patients in Group B and Group C were anesthetized with 0.5 μg/kg and 1.0 μg/kg dexmedetomidine infusion before anesthetic induction with sevoflurane in oxygen by face mask.The changes in hemodynamics and BIS were observed at time points before induction (T0 ), after induction (T1 ), and 5 min (T2 ) after intubation. Time going into sleep, time for the BIS to 60, time carrying intubation, anesthesia and operation, times carrying vital capacity breath ,and the adverse effect were also observed.RESULTS: Compared with the values at T0, the BIS, the heart rate and blood pressure were decreased remarkably at T1 (P<0.05). At T2 , the blood pressure was significantly higher than those at T0 and T1 in Group A (P<0.05). Compared with Group A, the BIS, heart rate and blood pressure were lower in Groups B and C(P<0.05)at T1,T2. The time going into sleep, time for the BIS to 60 and time carrying intubation were shorter in Group B and C (P<0.05), especially in group C.CONCLUSION: Both dexmedetomidine 0.5 μg/kg and 1.0 μg/kg caused sedation and significantly decreased hemodynamics and stress reaction to endotracheal intubation during sevoflurane anesthesia induction.Dexmedetomidine 1.0 μg/kg was better than dexmedetomidine 0.5 μg/kg.Severe bradycardia and hypotension during anesthesia should be noticed.
    Domestic clinical research progress of photosensitive anticancer drugs
    WANG Zi-hao, WANG Xue-feng, JIANG Han, WANG Jina-dong, SHI Wei-bin
    2012, 17(1):  107-111. 
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    Photodynamic therapy has been commonly applied to the treatment of cancer among the national major hospitals, and the effect is obvious. As the center element of the photodynamic therapy, the research results of photosensitive drugs have also gained particular attention. This article begins with the introduction of photosensitive drug, tells the mechanisms of the photosensitive drug, and emphatically reviews the domestic clinical application in the therapy of photosensitive drugs on tumors in recent years.
    Clinical application of Flupirtine in pain management
    ZHANG Xiu-shuang, NI Jia-xiang
    2012, 17(1):  112-115. 
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    Flupirtine is a new type of non-opioid analgesics for the selective neuronal potassium channel opener, with effects of analgesia, muscle relaxation and neuroprotective. Its main indication is myosalgia relevant to muscle tension. Flupirtine can be used to treat various types of acute and chronic pain, such as: low back pain, headache, cancer pain, and so on. As analgesics, the efficacy of Flupirtine is certain with light side effects. This article mainly reviews the clinical application of Flupirtine in pain management.
    Advances of study on glucocorticoids in the treatment of rheumatoid arthritis
    LI Dan-dan, LU Jin-ming
    2012, 17(1):  116-120. 
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    The glucocorticoids treat on patients with rheumatoid arthritis (RA) had a more than sixty years history, due to glucocorticoids have some side effects, different rheumatologists have different opinions. According to some clinical research for the past few years, glucocorticoids can improve the condition and inhibit the damage of join. This article is a review about the clinical effects and side effects of treatment for RA with glucocorticoids