Objective To explore the related factors of anxiety and gloomy mentality people aged 60-80 years and investigate the effectiue methods to intervention.Methods A follow-up study was proportional and carried out in Xicheng district of Beijing.Multi-phase,stratified,unequal cluster sampling was adopted to investigate old people in 2011 with WHO-QOL,Memorial University of Newfoundl and Scale of Happiness,Social Support Rating Scale,Self-Rating Anxiety Scale and Self-rating Depression Scale.2342 old people were randomly divided into control group and trial group.The trial group received health education,community social support,lightening the psychological stress in face to face,psychology guiding and group discussion.The control group received general observation only.Results Among 2342 old people,126 (5.3％) obtained anxiety and 201(8.6％) had gloomy mentality.The anxiety in the elderly was significantly related to age,marriment,culture,job,family type,family relationship,housing,income,medical insurance,retirement type,reading,keeping pets,character,training,feeling adjusting,life quality,subjective well-being,social support,depression (all P ＜ 0.05).The depression in the elderly was significantly related to gender,marriment,culture,job,family type,family relationship,housing,income,medical insurance,retirement type,reading,watching plays,character,feeling adjusting,drinking,training,life quality,subjective well-being,social support,anxiety (all P＜0.05).Scores of two groups had no significant difference before intervention.The change in scores of anxiety and depression in the trial group was obviously lower than in control group (P＜0.05).Conclusions The anxiety and gloomy mentality are common in old people aged 60-80 years in Xicheng District,which independently associated with related factors such as life quality,subjective well-being,social support and so on.After 6 months of treatment,the scores of anxiety and depression in the trial group is obviously lower than in control group.

Objective To study the pharmacokinetics of sodium aesci-nate after intravenous infusion in Chinese healthy volunteers. Methods Sodium aescinate for injection were given to 9 healthy volunteers of a single dose of 10 mg, the concentrations of aescinate in human plasma and urine were determined by HPLC-MS/MS, the main pharmacokinetic parameters were calculated with WinNonlin 5. 0. Results The main pharmacokinetic parameters of A ingredient of aescinate and B ingredient of aescinate were as follows: C_(max) were ( 283. 00 ± 70. 53 ), (206. 33 ± 57.20) ng · mL~(-1); AUC_(0-t) were (1008.05 ±396.49), (638.96 ± 259. 48) ng · h · mL~(-1);t_(1/2) were(3. 72 ±0. 44), (3.57 ±0.48) h;V_z were (19. 39 ±7. 05), (23.82 ±11.43) L;CL were (3. 66 ± 1. 36), (4. 55 ± 1. 86) L · h~(-1) ;36 hour accumulative urine excretion rates were (4. 91 ± 1. 38) % , (2. 80 ± 0. 71 ) % , respectively. Conclusion The disposing process of A ingredient of aescinate and B ingredient of aescinate in healthy subjects were resemble, the elimination half life was about 3. 6 h, the accumulative urine excretion rate was low.

Objective To investigate the effects and mechanisms of drug-containing serum of Buzhong Yiqi Decoction on the activity and vasculogenic mimicry(VM)of lung cancer cells.Meth-ods Drug-containing serum of Buzhong Yiqi Decoction with low-dose(BZ-L group),medium-dose(BZ-M group),and high-dose(BZ-H group)were prepared through gastric lavage in SD rats to inter-vene lung cancer cells.CCK-8 assay,Edu cell proliferation assay,cell clone formation assay,cell scratch assay,and Transwell assay were used to detect the effects of Buzhong Yiqi Decoction on the proliferation and migration of lung cancer A549 and HCC827 cells.Flow cytometry was employed to detect the impacts of Buzhong Yiqi Decoction on lung cancer cell apoptosis and cell cycle,and VM ex-periments in vitro were conducted to assess the effect of Buzhong Yiqi Decoction on angiogenesis in lung cancer cells.Differentially expressed genes between control cells and drug-intervened cells were detected by RNA-seq sequencing.Subcutaneous xenografts in mice were established to evaluate the in-hibitory effect of gavage therapy of Buzhong Yiqi Decoction on the growth of lung cancer cells in vivo.Results Buzhong Yiqi Decoction inhibited the viability and proliferative activity of A549 and HCC827 cells in a dose-dependent manner,promoted lung cancer cell apoptosis in a dose-dependent manner,and induced G2/M phase arrest.The migration ability of A549 and HCC827 cells was significantly reduced after Buzhong Yiqi Decoction intervention.As the concentration of Buzhong Yiqi Decoction increased,the VM of A549 and HCC827 cells gradually decreased.Compared with control cells,765 differentially expressed genes were identified in the Buzhong Yiqi Decoction group,with signifi-cant downregulation of p-JNK and p-ERK1/2 gene expression.Western blot analysis revealed that the phosphorylation level of the JNK/ERK1/2 signaling pathway in A549 and HCC827 cells was gradually inhibited with increasing concentrations of Buzhong Yiqi Decoction.Buzhong Yiqi Decoc-tion significantly reduced the volume and mass of mouse tumors,increased the apoptosis rate in tumor tissues,decreased the expression of p-JNK,p-ERK1,and p-ERK2,and increased the expression of E-cadherin in tumor tissues.Conclusion Buzhong Yiqi Decoction may inhibit the activity and angio-genesis of lung cancer cells by suppressing the activity of the JNK/ERK1/2 signaling pathway.

Objective To investigate the effects and mechanisms of drug-containing serum of Buzhong Yiqi Decoction on the activity and vasculogenic mimicry(VM)of lung cancer cells.Meth-ods Drug-containing serum of Buzhong Yiqi Decoction with low-dose(BZ-L group),medium-dose(BZ-M group),and high-dose(BZ-H group)were prepared through gastric lavage in SD rats to inter-vene lung cancer cells.CCK-8 assay,Edu cell proliferation assay,cell clone formation assay,cell scratch assay,and Transwell assay were used to detect the effects of Buzhong Yiqi Decoction on the proliferation and migration of lung cancer A549 and HCC827 cells.Flow cytometry was employed to detect the impacts of Buzhong Yiqi Decoction on lung cancer cell apoptosis and cell cycle,and VM ex-periments in vitro were conducted to assess the effect of Buzhong Yiqi Decoction on angiogenesis in lung cancer cells.Differentially expressed genes between control cells and drug-intervened cells were detected by RNA-seq sequencing.Subcutaneous xenografts in mice were established to evaluate the in-hibitory effect of gavage therapy of Buzhong Yiqi Decoction on the growth of lung cancer cells in vivo.Results Buzhong Yiqi Decoction inhibited the viability and proliferative activity of A549 and HCC827 cells in a dose-dependent manner,promoted lung cancer cell apoptosis in a dose-dependent manner,and induced G2/M phase arrest.The migration ability of A549 and HCC827 cells was significantly reduced after Buzhong Yiqi Decoction intervention.As the concentration of Buzhong Yiqi Decoction increased,the VM of A549 and HCC827 cells gradually decreased.Compared with control cells,765 differentially expressed genes were identified in the Buzhong Yiqi Decoction group,with signifi-cant downregulation of p-JNK and p-ERK1/2 gene expression.Western blot analysis revealed that the phosphorylation level of the JNK/ERK1/2 signaling pathway in A549 and HCC827 cells was gradually inhibited with increasing concentrations of Buzhong Yiqi Decoction.Buzhong Yiqi Decoc-tion significantly reduced the volume and mass of mouse tumors,increased the apoptosis rate in tumor tissues,decreased the expression of p-JNK,p-ERK1,and p-ERK2,and increased the expression of E-cadherin in tumor tissues.Conclusion Buzhong Yiqi Decoction may inhibit the activity and angio-genesis of lung cancer cells by suppressing the activity of the JNK/ERK1/2 signaling pathway.

Objective To examine the diagnosis and outcomes in the treatment of the patients with histologically confirmed central neurocytoma (CNC). Methods The data from 71 patients with CNC who were diagnosed between March 2003 and December 2007 were retrospectively evaluated. Various combinations of surgery, and radiotherapy had been used for treatment. Results The average bulk of tumors was 40 cm3. The median follow-up was 22 months. The 22 months overall survival and local control rate was 95.8%(68/71) and 95.6%(65/68), respectively. Conclusions The overall prognosis is favorable although the follow-up is not very long. Surgery and postoperative radiotherapy can significantly improve local control.

AIM To optimize the aqueous extraction for polysaccharides from Astragali Radix and to evaluate the in vitro antitumor activity.METHODS With extraction temperature,extraction time and solid-liquid ratio as influencing factors,extraction rate of polysaccharides as an evaluation index,the extraction was optimized by uniform design.The effect of polysaccharides on the proliferation of non-small cell lung cancer NCI-H460 cells,the apoptosis rate and cell cycle of NCI-H460 cells,and the expressions of Caspase-3,Bax and Bcl-2 were detected by MTT assay,flow cytometry and Western blot,respectively.RESULTS The optimal conditions were determined to be 100 ℃ for extraction temperature,1 h for extraction time,and 1 ∶ 35 for solid-liquid ratio,the extraction rate of polysaccharides was 3.62％.Compared with the control group,the proliferation of NCI-H460 cells was significandy inhibited in a dose-dependent manner (P ＜ 0.01),the S phase ratio,early apoptosis rate,late apoptosis rate and total apoptosis rate were markedly increased (P ＜ 0.01),and the Caspase-3 expression and Bax/Bcl-2 ratio were also obviously increased (P ＜ 0.01) in the polysaccharides group.CONCLUSION This fast,stable and reliable method can be used for the aqueous extraction for polysaccharides from Astragali Radix,which can significantly inhibit the proliferation of NCI-H460 cells and induce apoptosis of NCI-H460 cells.

OBJECTIVETo detect the expressions of CXCR4 and Nrf2 in non-small cell lung cancer (NSCLC) tissues and analyze their association with the clinicopathological features of NSCLC.

METHODSWe investigated the expressions of CXCR4 and Nrf2 in 66 NSCLC and corresponding distant normal tissue specimens using immunohistochemistry and real-time PCR.

RESULTSThe expressions of CXCR4 protein and mRNA were significantly higher in NSCLC tissue specimens than in the distant normal tissues, while the expression of Nrf2 protein and mRNA increased significantly in NSCLC tissues compared to those in the distant normal tissues (P<0.01). A high expression level of CXCR4 was positively correlated with a large tumor size (P=0.048), poor differentiation (P=0.024), advanced TNM stage (P=0.018), lymph node metastasis (P=0.004), and distant metastasis (P=0.016). The expression of Nrf2 protein was positively correlated with a large tumor size (P=0.008), advanced TNM stage (P=0.028), lymph node metastasis (P=0.038), and distant metastasis (P=0.023). A strong correlation was found between CXCR4 and Nrf2 expressions in NSCLC tissues (r=0.324, P<0.01), and the co-expression of CXCR4 and Nrf2 was strongly correlated with lymph node metastasis and distant metastasis.

CONCLUSIONAbnormal expressions of CXCR4 and Nrf2 may contribute to the progression and malignant biological behavior of NSCLC.

Carcinoma, Non-Small-Cell Lung ; metabolism ; pathology ; Female ; Gene Expression Regulation, Neoplastic ; Humans ; Lung Neoplasms ; metabolism ; pathology ; Lymphatic Metastasis ; Male ; Middle Aged ; NF-E2-Related Factor 2 ; metabolism ; Neoplasm Staging ; Receptors, CXCR4 ; metabolism ; Signal Transduction

Objective To study the pharmacokinetics of amlodipine besylate and folic acid tablet in Chinese healthy volunteers.Methods A single administration of two tests and one reference formulation was given to 24 healthy volunteers by oral according to a self -control, three periods, Latin square design study.The concentrations of amlodipine were determined by LC-MS/MS method.Results The main pharma-cokinetic parameters of amlodipine were as follows: AUC0-t were (115.30 ±28.12),(119.42 ±32.80),(113.19 ±27.08) ng · mL-1 · h;Cmax were (2.59 ±0.60), (2.59 ±0.50), (2.56 ±0.59) ng· mL-1;t1/2 were(38.90 ±9.27), (33.85 ±11.31),(40.66 ±7.05) h for two test and one reference formulation, respectively.Conclusion There is no significant difference between the main pharmacokinetic parameters of three formulations.

Objective To detect the expressions of CXCR4 and Nrf2 in non-small cell lung cancer (NSCLC) tissues and analyze their association with the clinicopathological features of NSCLC. Methods We investigated the expressions of CXCR4 and Nrf2 in 66 NSCLC and corresponding distant normal tissue specimens using immumohistochemistry and real-time PCR. Results The expressions of CXCR4 protein and mRNA were significantly higher in NSCLC tissue specimens than in the distant normal tissues, while the expression of Nrf2 protein and mRNA increased significantly in NSCLC tissues compared to those in the distant normal tissues (P<0.01). A high expression level of CXCR4 was positively correlated with a large tumor size (P=0.048), poor differentiation (P=0.024), advanced TNM stage (P=0.018), lymph node metastasis (P=0.004), and distant metastasis (P=0.016). The expression of Nrf2 protein was positively correlated with a large tumor size (P=0.008), advanced TNM stage (P=0.028), lymph node metastasis (P=0.038), and distant metastasis (P=0.023). A strong correlation was found between CXCR4 and Nrf2 expressions in NSCLC tissues (r=0.324, P<0.01), and the co-expression of CXCR4 and Nrf2 was strongly correlated with lymph node metastasis and distant metastasis. Conclusion Abnormal expressions of CXCR4 and Nrf2 may contribute to the progression and malignant biological behavior of NSCLC.

Objective To detect the expressions of CXCR4 and Nrf2 in non-small cell lung cancer (NSCLC) tissues and analyze their association with the clinicopathological features of NSCLC. Methods We investigated the expressions of CXCR4 and Nrf2 in 66 NSCLC and corresponding distant normal tissue specimens using immumohistochemistry and real-time PCR. Results The expressions of CXCR4 protein and mRNA were significantly higher in NSCLC tissue specimens than in the distant normal tissues, while the expression of Nrf2 protein and mRNA increased significantly in NSCLC tissues compared to those in the distant normal tissues (P<0.01). A high expression level of CXCR4 was positively correlated with a large tumor size (P=0.048), poor differentiation (P=0.024), advanced TNM stage (P=0.018), lymph node metastasis (P=0.004), and distant metastasis (P=0.016). The expression of Nrf2 protein was positively correlated with a large tumor size (P=0.008), advanced TNM stage (P=0.028), lymph node metastasis (P=0.038), and distant metastasis (P=0.023). A strong correlation was found between CXCR4 and Nrf2 expressions in NSCLC tissues (r=0.324, P<0.01), and the co-expression of CXCR4 and Nrf2 was strongly correlated with lymph node metastasis and distant metastasis. Conclusion Abnormal expressions of CXCR4 and Nrf2 may contribute to the progression and malignant biological behavior of NSCLC.