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1.
Med Sci Monit ; 30: e943196, 2024 Feb 13.
Article in English | MEDLINE | ID: mdl-38347712

ABSTRACT

BACKGROUND Ankylosing spondylitis (AS), a chronic inflammatory disease predominantly causing back pain, affects up to 0.5% of the global population, more commonly in males. Frequently undiagnosed in early stages, AS is often associated with comorbid depression and anxiety, imposing significant healthcare burdens. Despite available pharmaceutical treatments, exercise therapy (ET) has emerged as an effective, side-effect-free alternative, particularly for managing AS-induced back pain. This study aims to explore the research trends in ET for treating AS back pain from 2004-2023. MATERIAL AND METHODS A comprehensive analysis of 437 articles, sourced from the Science Citation Index-Expanded within the Web of Science Core Collection, was conducted using CiteSpace 6.2.R5. This study spanned from 2004 to October 15, 2023, examining publications, authors, institutions, and keywords to assess keyword co-occurrences, temporal progressions, and citation bursts. RESULTS Research interest in ET for AS began escalating around 2008 and has since shown steady growth. The USA emerged as a significant contributor, with Van der Heijde, Desiree, and RUDWALEIT M being notable authors. Key institutions include Assistance Publique Hopitaux Paris and UDICE-French Research Universities, with ANN RHEUM DIS being the most influential journal. The field's evolution is marked by interdisciplinary integration and branching into various sub-disciplines. CONCLUSIONS Exercise therapy for AS-induced back pain is a growing research area, necessitating further exploration in clinical management and rehabilitation strategies. The relationship between ET and osteoimmunological mechanisms remains a focal point for future research, with a trend towards personalized and interdisciplinary treatment approaches.


Subject(s)
Spondylitis, Ankylosing , Male , Humans , Spondylitis, Ankylosing/therapy , Exercise Therapy , Exercise , Back Pain/therapy , Bibliometrics
2.
Chinese Journal of Trauma ; (12): 500-507, 2023.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-992627

ABSTRACT

Objective:To explore the clinical outcomes of intraoperative fluoroscopy on femoral tunnel placement in treating professional snow sports athletes with anterior cruciate ligament (ACL) injury.Methods:A retrospective case series study was used to analyze the clinical data of 13 professional snow sports athletes with ACL injury treated in the National Institute of Sports Medicine, General Administration of Sport of China from January 2016 to January 2019. There were 5 males and 8 females, aged 16-27 years [(18.5±3.0)years]. Intraoperative lateral fluoroscopy combined with quadrant method was performed for the accurate femoral tunnel placement in single-bundle ACL reconstruction by using autologous hamstring tendon in all patients. KT1000 side-to-side difference (KT1000-ssd), pivot shift test, International Knee Documentation Committee (IKDC) subjective score, Lysholm score, Marx activity scale and maximum extension and flexion resistance ratio of the involved and uninvolved knee were compared before operation (or before injury) and at 3, 6, 12 and 24 months after operation. Whether returning to the field, time taken in returning to the field and re-injury were recorded at each follow-up visit. ACL graft signal intensity ratio (SIR) in MRI of the involved knee was evaluated at postoperative 24 months.Results:All patients were followed up for 24-33 months [(25.8±2.7)months]. There were 7 patients with KT1000-ssd degree I, 5 with degree II and 1 with degree III before operation, compared to 12 patients with KT1000-ssd degree 0 and 1 with degree I at 3 and 6 months after operation and 13 patients with KT1000-ssd degree 0 at 12 and 24 months after operation. The pivot shift test was grade I in 8 patients and grade II in 5 before operation, compared to 11 patients with degree 0 and 2 with degree I at 3 months after operation and 12 patients with degree 0 and 1 with degree I at 6, 12 and 24 months after operation. IKDC subjective score was (68.0±4.3)points, (84.7±7.9)points, (94.6±3.3)points and (96.5±1.8)points at postoperative 3, 6, 12 and 24 months, respectively. Six months after operation, IKDC subjective score was significantly improved compared to the preoperative (48.3±25.0)points (all P<0.01). The Lysholm score was (63.4±6.6)points, (80.1±6.5)points, (93.8±4.6)points and (96.5±2.4)points at postoperative 3, 6, 12 and 24 months, respectively. Six months after operation, the Lysholm score was significantly improved compared to the preoperative (47.5±29.4)points (all P<0.01). The Marx activity scale was (7.4±0.5)points, (13.8±0.7)points, (14.6±0.8)points and (15.0±0.7)points at postoperative 3, 6, 12 and 24 months, respectively, significantly lower than (16.0±0.0)points before the injury (all P<0.01). The maximum extension resistance ratio of the involved and uninvolved knee was 0.60±0.10, 0.85±0.08, 0.91±0.06 and 0.97±0.04 at postoperative 3, 6, 12 and 24 months, respectively. Six months after operation, the maximum extension resistance ratio of the involved and uninvolved knee was significantly increased compared to the preoperative 0.57±0.18 (all P<0.01).The maximum flexion resistance ratios of involved and uninvolved knee were 0.64±0.09, 0.82±0.06, 0.89±0.04 and 0.94±0.06 at postoperative 3, 6, 12 and 24 months, respectively. Six months after operation, the maximum flexion resistance ratio of the involved and uninvolved knee was significantly increased compared to the preoperative 0.60±0.12 (all P<0.01). Thirteen athletes returned to the field within 12 months after operation with the time taken in returning to the field ranging from 5-12 months [(8.7±1.9)months]. There was no ACL re-injury at postoperative 24 months. The ACL graft SIR in MRI of the involved knee was 1.80±0.20 at postoperative 24 months. Conclusion:Intraoperative fluoroscopy on femoral tunnel placement in the treatment of professional snow sports athletes with ACL injury can significantly improve the knee joint stability, subjective function, sports performance and muscle strength within 6 months, and can help them return to the field within 12 months, and accelerates graft healing.

4.
Journal of Preventive Medicine ; (12): 255-259, 2017.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-792604

ABSTRACT

Objective To develop the eye health related behaviors questionnaire for school age children and to evaluate its reliability and validity.Methods The initial questionnaire was formulated by literature review,preliminary-work outcomes and expert consultation.Totally 288 students in 4-5 grades from a elementary school in Wenzhou were selected.Two-independent samples t-test,pearson correlation coefficient analysis,test of internal consistency and factor analysis were conducted to examine the reliability and validity.Results Eye health related behaviors questionnaire for school age children was consisted of 28 items and 3 dimensions.Exploratory factor analysis suggested that 7 factors accounted for 63.76% of the accumulated variances.The questionnaire-level content validity index was 0.89.The Cronbach's α coefficient was 0.82,and the spilt-half reliability coefficient was 0.844.The test-retest reliability coefficient was 0.682.Conclusion Eye health related behaviors questionnaire for school age children has good reliability and validity,which could be applied to measure children's eye health related behaviors.

5.
Clin Res Hepatol Gastroenterol ; 39(5): 610-9, 2015 Oct.
Article in English | MEDLINE | ID: mdl-25726501

ABSTRACT

BACKGROUND: Ischemia and reperfusion (I/R) injury is one of the main lesions after liver transplantation. This study aims to detect hypoxia-induced HIF-1α protects transplanted liver against I/R injury by promoting glucose metabolism to decrease mitochondrial injury and apoptosis on rat model. METHODS: The rats were given a treatment of 90 min non-lethal hypoxic preconditioning to induce and increase the HIF-1α expression. The autologous orthotopic liver transplantation model was used to imitate liver I/R injury. RESULTS: Hypoxic-induced HIF-1α was detected to increase in liver tissue after 90-minute hypoxic environment (HP vs. Ctrl, *P<0.001). After operation, the expression of HIF-1α in liver tissue was also stayed at a high level. At 24h after operation, several genes were promoted, such as the levels of HK-2 (HP vs. AT, 24h, *P=0.004), Lactate dehydrogenase (LDHA) (HP vs. AT, 24h, *P=0.003), pyruvate dehydrogenase kinase (PDK-1) (HP vs. AT, 24h, *P=0.007), even the NF-κB and Erk pathways. From the TUNEL assay, the apoptosis in hypoxic preconditioning liver tissue was decreased compared with non-HP operative group at 12h after operation. The expressions of cleaved-caspase 3 (HP vs. AT, *P=0.0119) and PARP (HP vs. AT, *P=0.0134) in HP group were also significantly lower than AT group. CONCLUSION: The hypoxia-induced HIF-1α could promote glucose metabolism to protect hepatocellular mitochondria from damage. It could be a useful way to protect liver against I/R injuries and inflammatory injury, and particularly promote the recovery of graft function.


Subject(s)
Glucose/metabolism , Hypoxia-Inducible Factor 1, alpha Subunit/biosynthesis , Ischemic Preconditioning , Liver Transplantation , Mitochondria/metabolism , Reperfusion Injury/prevention & control , Animals , Biomarkers/metabolism , Disease Models, Animal , Female , Gene Expression Regulation , Hypoxia-Inducible Factor 1, alpha Subunit/genetics , Random Allocation , Rats , Rats, Sprague-Dawley , Signal Transduction
6.
Chin J Integr Med ; 20(7): 534-9, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24420925

ABSTRACT

OBJECTIVE: To evaluate the effect of a 10-day course of triptolide (TP) on rat cytochrome (CY) P3A4 activity, and on the pharmacokinetics of cyclophosphamide (CPA). METHODS: In the pharmacokinetics experiment, rats were orally given 0.9% NaCl solution (n=5) and TP [1.2 (mg/kg·d)] for 10 days and a single dose of CPA was administered intravenously (100 mg/kg) to rats on day 11. Blood samples were collected up to 4 h at predetermined time intervals, the plasma concentration of CPA was determined by high performance liquid chromatography (HPLC) and pharmacokinetic parameters were determined. In the in vitro CYP3A4 activity inhibition research, rat blank liver microsomes were divided into 3 groups: a control group, a TS (5 µL, 200 µmol/L) with TP (5 µL, 12.5 µmol/L) group, a TS with ketoconazole (5 µL, 1 µmol/L) group. Concentration of 6ß-hydroxylated testosterone (6ß-OHT) in liver microsomes was measured by HPLC and the activity of CYP 3A4 was calculated through the following formula: Einhibitor/Econtrol × 100%=Cinhibitor/Ccontrol × 100%. RESULTS: Compared with the control group, the area under the plasma concentration-time curve (AUC0-∞) of CPA was significantly increased by 229.05% pretreated with TP (P<0.01). Peak plasma concentrations (Cmax) of CPA was significantly increased and plasma half-life was correspondingly extended. The CYP3A4 activity was significantly inhibited by ketoconazole 93.5%±0.2% and TP 84.6%±0.3% compared with the control group (P<0.01 and P<0.05, respectively). CONCLUSION: Our results strongly suggested that long-term oral intake of TP can distinctly inhibit the CYP3A4 activity and this inhibition evidently decrease the formation of toxic metabolites of CPA.


Subject(s)
Cyclophosphamide/pharmacokinetics , Cytochrome P-450 CYP3A Inhibitors/pharmacology , Cytochrome P-450 CYP3A/metabolism , Diterpenes/pharmacology , Herb-Drug Interactions , Immunosuppressive Agents/pharmacokinetics , Phenanthrenes/pharmacology , Animals , Epoxy Compounds/pharmacology , Hydroxytestosterones/metabolism , Injections, Intravenous , Ketoconazole/pharmacology , Male , Microsomes, Liver/drug effects , Microsomes, Liver/metabolism , Rats, Sprague-Dawley
7.
Article in English | WPRIM (Western Pacific) | ID: wpr-267167

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the effect of a 10-day course of triptolide (TP) on rat cytochrome (CY) P3A4 activity, and on the pharmacokinetics of cyclophosphamide (CPA).</p><p><b>METHODS</b>In the pharmacokinetics experiment, rats were orally given 0.9% NaCl solution (n=5) and TP [1.2 (mg/kg·d)] for 10 days and a single dose of CPA was administered intravenously (100 mg/kg) to rats on day 11. Blood samples were collected up to 4 h at predetermined time intervals, the plasma concentration of CPA was determined by high performance liquid chromatography (HPLC) and pharmacokinetic parameters were determined. In the in vitro CYP3A4 activity inhibition research, rat blank liver microsomes were divided into 3 groups: a control group, a TS (5 μL, 200 μmol/L) with TP (5 μL, 12.5 μmol/L) group, a TS with ketoconazole (5 μL, 1 μmol/L) group. Concentration of 6β-hydroxylated testosterone (6β-OHT) in liver microsomes was measured by HPLC and the activity of CYP 3A4 was calculated through the following formula: Einhibitor/Econtrol × 100%=Cinhibitor/Ccontrol × 100%.</p><p><b>RESULTS</b>Compared with the control group, the area under the plasma concentration-time curve (AUC0-∞) of CPA was significantly increased by 229.05% pretreated with TP (P<0.01). Peak plasma concentrations (Cmax) of CPA was significantly increased and plasma half-life was correspondingly extended. The CYP3A4 activity was significantly inhibited by ketoconazole 93.5%±0.2% and TP 84.6%±0.3% compared with the control group (P<0.01 and P<0.05, respectively).</p><p><b>CONCLUSION</b>Our results strongly suggested that long-term oral intake of TP can distinctly inhibit the CYP3A4 activity and this inhibition evidently decrease the formation of toxic metabolites of CPA.</p>


Subject(s)
Animals , Male , Cyclophosphamide , Pharmacokinetics , Cytochrome P-450 CYP3A , Metabolism , Cytochrome P-450 CYP3A Inhibitors , Pharmacology , Diterpenes , Pharmacology , Epoxy Compounds , Pharmacology , Herb-Drug Interactions , Hydroxytestosterones , Metabolism , Immunosuppressive Agents , Pharmacokinetics , Injections, Intravenous , Ketoconazole , Pharmacology , Microsomes, Liver , Metabolism , Phenanthrenes , Pharmacology , Rats, Sprague-Dawley
8.
Chinese Journal of Dermatology ; (12): 160-163, 2013.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-432303

ABSTRACT

Objective To determine the expression of miR-486-3p in psoriatic lesions and healthy human skin and to estimate its effect on keratin 17 (K17) expression in HaCaT human keratinocytes.Methods Bioinformatics was used to predict microRNAs that may affect the expression of K17.Tissue samples were obtained from the lesions of 10 patients with psoriasis and normal skin of 10 healthy human controls.RNA was extracted from these tissue samples and reversely transcribed into cDNA with the addition of a Poly (A) tail.Then,real time quantitative PCR was performed to measure the expression of miR-486-3p.Cultured keratinocytes were transfected with miR-486-3p mimics or negative control,and Western blot was performed to determine K17 expression at 48 hours after the transfection.To evaluate the inhibitory effect of miR-486-3p on K17 expression,cultured 293T cells were transfected with the plasmid containing K17 3' untranslated region (UTR) seed sequence,three plasmids containing the complete deletion,interval mutation or double repeats of the seed sequence,or negative control plasmid.At 24 hours after the transfection,a dualluciferase reporter (DLR) assay was performed to quantify the expression of K17.Results Real time PCR showed that the expression level of miR-486-3p was significantly lower in psoriatic lesions than in the normal skin (0.211 ± 0.120vs.0.555 ± 0.425,t =2.62,v =9,P < 0.05).The HaCaT cells transfected with the mimics of miR-486-3p exhibited decreased expression of K17 compared with those transfected with the negative control.DLR assay revealed that the expression level (fluorescence intensity) of K17 in the negative control group was significantly higher than that in the 293T cells transfected with the seed sequence and those with the double repeats of the seed sequence (100.00% vs.65.31% ± 6.32% and 54.18% ± 10.01% respectively,both P < 0.05),but did not differ from that in the 293T cells transfected with the complete deletion and interval mutation of the seed sequence (100.00% vs.114.77% ± 16.14% and 110.21% ± 12.99% respectively,both P > 0.05).Conclusions The expression of miR-486-3p,which may inhibit K17 expression by binding to the seed sequence of K17 3'UTR,is lower in psoriatic lesions than in normal skin.The decreased expression and inhibitory effect of miR-486-3p may be implicated in the initiation and progression of psoriasis.

9.
J Hazard Mater ; 187(1-3): 509-16, 2011 Mar 15.
Article in English | MEDLINE | ID: mdl-21315512

ABSTRACT

C-doped TiO(2) nanoparticles prepared by partial oxidation of TiC were modified with Pt species by impregnation-calcination method in order to enhance the visible light photocatalytic activity. The physicochemical properties of as-prepared samples were characterized by various techniques in detail. The results indicated that a novel Pt/C-doped TiO(2)/PtCl(4) three-component nanojunction system was formed, where C-doped TiO(2) and PtCl(4) behaved as two visible light responsive components, and Pt metal as electron-transfer system. The three-component nanojunctioned photocatalyst system exhibited six times higher visible light activity than that of the pristine C-doped TiO(2) in degradation of toluene in air. The dramatically enhanced activity can be attributed to the increased utilization of visible light, the enhanced charge carrier separation and transfer process. Further more, the band structure and photocatalysis mechanism over the three-component nanojunction system was proposed and discussed. This work may provide new insights into the design of novel multi-component photocatalyst system with efficient visible light activity.


Subject(s)
Air Pollutants/chemistry , Light , Photochemistry , Platinum Compounds/chemistry , Titanium/chemistry , Toluene/chemistry , Catalysis , Kinetics , Microscopy, Electron, Transmission , Spectrum Analysis , X-Ray Diffraction
10.
Clinical Medicine of China ; (12): 1301-1303, 2010.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-385187

ABSTRACT

ObjectiveTo study the Electrocardiogram (ECG) changes in AIDS patients at different age grades. MethodsThe ECG of 400 AIDS patients at different age were analyzed retrospectively. Results(①)The rate of abnormal ECG in the age group of 46 ~50 years was significantly higher than 11 ~ 15(P =0. 008) ,21 ~25( P = 0. 041 ),31 ~ 35 ( P = 0. 022 ),41 ~ 45 ( P = 0. 001 ) and 51 ~ 55 ( P = 0. 047 ) years groups respectively. (②)The rate of bradyarrhythmia in the age group of 46 ~ 50 years was significantly higher than 31 ~ 35 (U = 2. 44) ,36 -40( U = 2. 18 ) ,41 ~ 45 ( U = 2. 57 ) years groups ( P < 0. 05 respectively. (③)The rate of left atrial and ventricular hypertrophy in 11 ~ 15 years group was significantly lower than the age groups older than 46 (except for 51 ~ 55years group) ;those aged >60 had higher atrial and ventricular hypertrophy rate than 36 ~40,41 ~45 and 51 ~55years groups ( P < 0. 05 respectively). ConclusionsAIDS patients at all ages may present abnormal ECG, which is positively correlated with age.

11.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-548217

ABSTRACT

Objcetive: To investigate the effect of resveratrol (RES)combined with cisplatin (DDP)on the cholangiocarcinoma cell line FRH-0201 in vitro. Methods: FRH-0201 cells were exposed to different concentrations of RES or (and)DDP. Cell morphological changes were observed by light and fluorescence microscopy. Inhibition of cell proliferation was measured by MTT and colony-forming assay. And the flow cytometry were performed to detect the cell apoptosis rate and cell cycle. Results: Resveratrol inhibited the proliferation of FRH-0201 cells in a time-and dose-dependent manner in the concentration of 5~320 ?mol/L and the IC50 values after the exposure of 24, 48, and 72 h were 55.35, 32.84, and 28.01 ?mol/L respectively. RES and DDP had synergetic effect in the inhibition of FRH-0201 cells. Conclusion: RES can inhibit the growth of FRH-0201 cells and has the synergetic effect with DDP.

12.
Chinese Journal of Oncology ; (12): 317-319, 2008.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-348103

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the efficacy and safety of a weekly schedule of low dose-intensity docetaxel monochemotherapy for patients with anthracycline-resistant metastatic breast cancer (MBC) in poor physical status.</p><p><b>METHODS</b>Thirty MBC patients who were previously exposed to anthracycline treatment received docetaxel alone at a dose of 30 mg/m2 on D1, D8 and D15, repeated every 4 weeks for a maximum of 6 cycles.</p><p><b>RESULTS</b>Of the 30 evaluable patients, 2 (6.7%) achieved a complete response, and 9 (30.0%) a partial response, with an overall objective response rate of 36.7% (95% CI: 20.5%-53.9%). The most common adverse event was hematologic toxicity. After an average follow-up of 15.0 months, the median time to progression (TTP) was 8. 5 months and the median overall survival (OS) had not reached yet at the end of follow-up.</p><p><b>CONCLUSION</b>The weekly low dose-intensity docetaxel monochemotherapy is effective and well-tolerated in patients with anthracycline-resistant metastatic breast cancer in poor physical status.</p>


Subject(s)
Adult , Aged , Female , Humans , Middle Aged , Anthracyclines , Therapeutic Uses , Antineoplastic Agents , Therapeutic Uses , Breast Neoplasms , Drug Therapy , Pathology , Carcinoma, Ductal, Breast , Drug Therapy , Pathology , Carcinoma, Lobular , Drug Therapy , Pathology , Drug Resistance, Neoplasm , Follow-Up Studies , Leukopenia , Lymphatic Metastasis , Nausea , Neoplasm Metastasis , Neoplasm Staging , Remission Induction , Survival Rate , Taxoids , Therapeutic Uses
13.
Chinese Journal of Oncology ; (12): 741-744, 2008.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-357349

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the expressions of TopI gene in small cell lung cancer cell line H446, and explore the influence of TopI on the chemosensitivity of the cell line to topotecan (TPT).</p><p><b>METHODS</b>Western blot was performed to detect the TopI expression in H446 cells. Lipofectamine 2000 was used for the transient transfection of H446 cells by siRNA, and the transfection efficacy was detected. TopI mRNA was analyzed by quantitative RT-PCR and TopI protein was detected by Western blot to selected effective siRNA. The drug-sensitivity to topotecan (TPT) was evaluated by MTT assay.</p><p><b>RESULTS</b>TopI gene was expressed in H446 cells. Lipofectamine 2000 mediated the siRNA effectively (88.67%). Compared with its parental cells, RT-PCR results showed that TopI mRNAs in transfected cells were reduced by (95.7 +/- 1.6)%, (90.8 +/- 1.6)%, (96.1 +/- 2.7)% and (96.3 +/- 1.8)%, respectively, and decreased significantly at protein level. By MTT assay, the inhibition rate of TPT to H446 cells transfected by siRNA was lower than that of control group at same concentrations (P < 0.01).</p><p><b>CONCLUSION</b>siRNAs can silence the expression of TopI and decrease the drug-sensitivity of H446 cells to TPT.</p>


Subject(s)
Humans , Antineoplastic Agents , Pharmacology , Cell Line, Tumor , Cell Proliferation , DNA Topoisomerases, Type I , Genetics , Metabolism , Down-Regulation , Drug Resistance, Neoplasm , Lung Neoplasms , Metabolism , Pathology , RNA Interference , RNA, Messenger , Metabolism , RNA, Small Interfering , Genetics , Small Cell Lung Carcinoma , Metabolism , Pathology , Topotecan , Pharmacology , Transfection
14.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-281517

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the mechanism of hyperlipidemia- and imflammation-induced functional impairment of the endothelium.</p><p><b>METHODS</b>The experiment was conducted using 3 groups of rats fed for 20 weeks with standard chow (control group), high-fat diet and high-fat diet with daily fenofibrate treatment (10 mg/kg, starting since the fifth week), respectively. After 4 and 20 weeks of feeding, respectively, serum lipid level and NO concentration were measured in the rats, and the epithelial vascular cell adhesion molecule-1 (VCAM-1) expression and cell adhesiveness to the aortic endothelium were observed.</p><p><b>RESULTS</b>Compared with the control group, the rats with hyperlipidemia induced by long-term high-fat diet feeding showed lower NO concentration and increased leukocyte accumulation on the endothelial surface, exhibiting also stronger and more extensive endothelial expression of VCAM-1. In contrast, the hyperlipidemic rats with fenofibrate treatment shoed significantly decreased VCAM-1 expression and leukocyte adhesion with recovery of the NO level.</p><p><b>CONCLUSION</b>NO deficiency and activation of inflammation are involved in vascular impairment in rats with high-fat diet-induced hyperlipidemia, and fenofibrate can effectively prevent atherosclerosis by restoring NO concentration and down-regulating VCAM-1 expression in these rats.</p>


Subject(s)
Animals , Rats , Atherosclerosis , Cell Adhesion , Endothelium, Vascular , Metabolism , Fenofibrate , Pharmacology , Hyperlipidemias , Drug Therapy , Metabolism , Inflammation , Leukocytes , Cell Biology , Nitric Oxide , Metabolism , Rats, Sprague-Dawley , Vascular Cell Adhesion Molecule-1 , Metabolism
15.
Chinese Journal of Oncology ; (12): 124-126, 2007.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-255707

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the expression and its significance of DNA topoisomerase I (Topo I) in small cell lung cancer (SCLC).</p><p><b>METHODS</b>Topo I expression was detected by immunohistochemical S-P technique on 50 cases of SCLC and 12 cases of normal lung tissues.</p><p><b>RESULTS</b>The total positive rate of Topo I in normal lung tissue was 25.0% (3/12) and 78.0% (39/50) in SCLC. The expression of Topo I does not correlate with age, gender, smoking, tumor size and tumor site (P > 0.05), but significantly correlated with lymph node metastasis and clinical stage (P <0.05).</p><p><b>CONCLUSION</b>High Topo I expression is a rationale indication of Topo I inhibitor treatment of malignancies. It should be possible to predict anti-tumor drug sensitivity by assessment of Topo I expression and help to improve the therapeutic efficacy for cancer patients.</p>


Subject(s)
Female , Humans , Male , Middle Aged , Carcinoma, Small Cell , Pathology , DNA Topoisomerases, Type I , Metabolism , Immunohistochemistry , Methods , Lung Neoplasms , Pathology , Lymphatic Metastasis , Neoplasm Staging
16.
Chinese Journal of Oncology ; (12): 746-749, 2006.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-316311

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the relationship between the expressions of integrin alpha5 beta1 and E-CD, and clinicopathological characteristics and prognosis of patients with non-small cell lung carcinoma (NSCLC).</p><p><b>METHODS</b>The expression of integrin alpha5 beta1 and E-CD were analyzed in 53 NSCLC and 12 control specimens by immunohistochemical assay.</p><p><b>RESULTS</b>The expression of integrin alpha5 beta1 was significantly higher in NSCLC (58.5%) than that in normal lung tissue (16.7%), and also positively related with pathological characteristics (P = 0.021), lymph node metastasis (P = 0.006), and clinical stage (P = 0.002). The 3-year survival rate in NSCLC group was significantly lower than that in control group (22.3% vs 40.6% , P = 0.041). The positive expression of E-CD in NSCLC and control group was 32.1% and 91.7%, respectively, and negatively correlated with pathological characteristics (P = 0.010) and lymph node metastasis (P = 0.002). The 3-year survival rate in control group was 19.9%, lower than that in NSCLC group (41.2%, P > 0.05), but the difference is not significant.</p><p><b>CONCLUSION</b>The overexpression of integrin alpha5 beta1 may contribute to lymph node metastasis and play an inverse role, while E-CD may be a beneficial prognostic factor in patients with NSCLC.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Cadherins , Metabolism , Carcinoma, Non-Small-Cell Lung , Metabolism , Pathology , Immunohistochemistry , Integrin alpha5beta1 , Metabolism , Lung Neoplasms , Metabolism , Pathology , Lymphatic Metastasis , Neoplasm Staging , Smoking , Survival Analysis
17.
Chinese Journal of Oncology ; (12): 377-379, 2005.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-358628

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effectiveness, safety and possible mechanism of recombinate human interleukin 11 (rhIL-11) in the treatment of chemotherapy-induced thrombocytopenia.</p><p><b>METHODS</b>Thirty-four patients (totally 76 cycles) with chemotherapy-induced thrombocytopenia received subcutaneous injection of rhIL-11 at the dose of 25 microg.kg(-1).d(-1) for 4 to 16 days. Serum IL-11 level was measured by ELISA, and IL-11 R alpha expression was detected by RT-PCR.</p><p><b>RESULTS</b>The mean baseline platelet count before chemotherapy was (135.0 +/- 54.3) x 10(9)/L for the 1st cycle and (259.4 +/- 64.5) x 10(9)/L for the 2nd cycle. The time to administer rhIL-11 was 7 to 16 days (median 12 days) in the 1st cycle and 4 to 10 days (median 6 days) in the 2nd, respectively (P < 0.05). The duration of post-chemotherapy platelet count below 50 x 10(9)/L was 7 to 13 days (median 10 days) for the 1st cycle and 3 to 8 days (median 5 days) for the 2nd, respectively (P < 0.05). Platelet count reached 300 x 10(9)/L or above in 30 chemotherapy cycles. The maximum platelet count was found to appear at D10 to D 17 (median D14), and negatively correlated with the pre-chemotherapy serum IL-11 level after administration of rhIL-11. Major adverse reactions included edema, headache, muscle and joint pain.</p><p><b>CONCLUSION</b>rhIL-11 is effective and safe for the treatment of chemotherapy-induced thrombocytopenia, with a relatively slow but sustained effect on the recovery of platelet count. Pre-chemotherpy serum IL-11 level might predict the efficacy of rhIL-11.</p>


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Antineoplastic Combined Chemotherapy Protocols , Therapeutic Uses , Breast Neoplasms , Drug Therapy , Carcinoma, Non-Small-Cell Lung , Drug Therapy , Injections, Subcutaneous , Interleukin-11 , Blood , Lung Neoplasms , Drug Therapy , Platelet Count , Recombinant Proteins , Thrombocytopenia , Drug Therapy , Treatment Outcome
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