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1.
Journal of Experimental Hematology ; (6): 1493-1497, 2017.
Article in Chinese | WPRIM | ID: wpr-301700

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the efficacy and safety of Shengxue mixture combined with intraosseous blood infusion for treatment of aplastic anemia patients.</p><p><b>METHODS</b>From 2011 to 2015, Institute of blood diseases of Shaanxi Medical University admitted 53 patients with aplastic anemia. The patients were treated with shengxue mixture 200 ml, orally, twice a day. Stanozolol tablets, Adult 2 mg, three times a day, mycophenolate mofetil 1.0 g, twice a day. Intraosseous infusion of the following medicine were administered in patients: recombinant human EPO 10000 U, recombinant human G-CSF 450 µg, recombinant human IL-11 4.5 mg, dexmethasone 20 mg, once a week, a total of four times. One month later, the blood cell counts and bone marrow biopsy were performed. Consolidation treatment continued for 3 to 6 months after discharge, and therapeutic effect was observed and followed-up for more than a year.</p><p><b>RESULTS</b>After one month of treatment, 40 patients were basically cured (75.47%), 8 patients were remitted(15.09%), Hemoglobin level, white blood cell count and platelet count were significantly improved after treatment (P<0.01). The overall response rate was 90.57%(48 patients). Patients with bone marrow hyperplasia was 46 (86.79%), versus 9(16.98%) before treatment. There was a difference (P<0.05). After 3 to 6 months of treatment, 40 patients were cured (75.47%); 8 patients were remitted(15.09%); 3 patients were obviously improved(5.66%); 2 patients were ineffective(3.77%). The overall response rate was 96.23%(51 cases). No obvious side effects were observed. No patients were relapsed after one year.</p><p><b>CONCLUSION</b>Shengxue mixture combined with Intraosseous infusion is a fast, efficient, safe method for the treatment of aplastic anemia.</p>

2.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 888-891, 2011.
Article in Chinese | WPRIM | ID: wpr-265792

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect and safety of haemostatic apozem combined with haemostatic mixture on hemophilia hemorrhage.</p><p><b>METHODS</b>Five hundred hemophilia patients were randomly recruited from Shaanxi Yida Hematology Institute from February 2005 to July 2010. Under the condition of using no blood products such as platelet cofactors VIII and IX, oral administration of haemostatic apozem combined with intravenous dripping of haemostatic mixture were given to 332 hemorrhagic patients and 451 patients in need of surgery for hemorrhagic prevention. The treatment was lasted for three successive weeks. The hemostatic time, hemorrhage absorption (recovery) time, and their safety were observed.</p><p><b>RESULTS</b>The hemostatic time for open bleeding and closed bleeding was (0.85 +/- 0.83) h and (2.69 +/- 0.65) h respectively. The average hemostatic time was (2.00 +/- 0.69) h. The recovery time for different portions was as follows respectively: intra-cranial hemorrhage (14.13 +/- 6.01) days; muscular hemorrhage (18.18 +/- 7.34) days; hematuria (8.25 +/- 4.69) days; arthrorrhagia(3.27 +/- 1.31) days; ecchymoma (7.16 +/- 2.32) days; bleeding of oral and nasal cavities (4.26 +/- 1.35) days; intramedullary hemorrhage (19.15 +/- 1.36) days; hematoma ulceration (50.01 +/- 20.91) days. The hemorrhage recovery ratio was 99.10% (329/332). The success rate of preventing from surgery hemorrhage was 100% (451/451). No severe adverse reaction occurred during the therapeutic course.</p><p><b>CONCLUSIONS</b>Haemostatic apozem combined with haemostatic mixture was effective and fast in preventing and treating hemophilia hemorrhage, with no complications or adverse reactions. It could be taken as the first choice for prevention and treatment of hemophilia hemorrhage.</p>


Subject(s)
Adolescent , Adult , Aged , Child , Child, Preschool , Female , Humans , Infant , Male , Middle Aged , Young Adult , Drugs, Chinese Herbal , Therapeutic Uses , Hemophilia A , Drug Therapy , Hemorrhage , Hemostatics , Therapeutic Uses , Phytotherapy
3.
Journal of Experimental Hematology ; (6): 69-73, 2009.
Article in Chinese | WPRIM | ID: wpr-302195

ABSTRACT

This study was aimed to investigate on effect of As(2)O(3) on expressions of COX-2, MMP-2 and MMP-9 in SGC7901 and K562 cells. SGC7901 and K562 cells were cultured in RPMI 1640 medium and were inoculated in culture medium with different concentrations of As(2)O(3) and at different times. Expressions of COX-2, MMP-2 and MMP-9 in SGC7901 and K562 cells were measured by using Western blot, while the levels of COX-2 mRNA and MMP-2 mRNA were measured with fluorescence quantitative RT-PCR. The results showed that the expression of COX-2, MMP-2 and MMP-9 decreased in dose- and time-dependent manners after treating with As(2)O(3). The levels of COX-2 mRNA and MMP-2 mRNA reduced in groups treated with As(2)O(3). In conclusion, As(2)O(3) inhibits expressions of COX-2, MMP-2 and MMP-9 in K562 and SGC7901 cells, suggesting that As(2)O(3) inhibits tumor development through its effect on angiogenesis involved in solid and hematologic malignancies.


Subject(s)
Humans , Arsenicals , Pharmacology , Cyclooxygenase 2 , Metabolism , Gene Expression Regulation, Leukemic , K562 Cells , Matrix Metalloproteinase 2 , Metabolism , Matrix Metalloproteinase 9 , Metabolism , Oxides , Pharmacology
4.
Journal of Experimental Hematology ; (6): 1303-1307, 2008.
Article in Chinese | WPRIM | ID: wpr-234245

ABSTRACT

This study was aimed to investigate the effect of arsenic trioxide (As2O3) on expression of vascular endothelial growth factor-C (VEGF-C) and its receptor VEGFR-3 in gastric cancer in order to clarify the role of As2O3 in lymphangiogenesis and metastasis of tumor. The gastric cancer model was established in nude mice by using gastric cancer cell line SGC-7901. As2O3 was injected to the two treatment groups (2.5 mg/kg and 5 mg/kg) and the same volume of saline solution was injected to the control group. Expression of VEGF-C and VEGFR-3 were detected by immunohistochemistry and were analyzed with QWin550cW image Acquiring & Analysis System. The results showed that the expression of VEGF-C and VEGFR-3 in cancer cells significantly reduced in the arsenic -treated groups. The expression of VEGF-C and VEGFR-3 in 5 mg/kg group was significantly less than that in 2.5 mg/kg group. The gray ratio analysis confirmed that there were significant difference between control group and two treated group, as well as between 2.5 mg/kg-treated group and 5 mg/kg-treated group. It is concluded that As2O3 can inhibit expression of VEGF-C and VEGFR-3 of human gastric cancer xenografts in nude mice, which suggests that As2O3 may inhibit the lymphangiogenesis by suppressing the expression of VEGF-C and VEGFR-3.


Subject(s)
Animals , Humans , Male , Mice , Arsenicals , Pharmacology , Cell Line, Tumor , Mice, Nude , Oxides , Pharmacology , Stomach Neoplasms , Metabolism , Vascular Endothelial Growth Factor C , Metabolism , Vascular Endothelial Growth Factor Receptor-3 , Metabolism , Xenograft Model Antitumor Assays
5.
Chinese journal of integrative medicine ; (12): 301-305, 2007.
Article in English | WPRIM | ID: wpr-282388

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect and safety of graded therapy featuring integrative traditional Chinese and Western medicine for the treatment of hemophilic arthritis.</p><p><b>METHODS</b>Forty patients with hemophilic arthritis were hospitalized randomly, with their blood coagulation factor activity determined by one-stage method and their arthritis classified into 4 stages. The treatment was applied according to the stage of arthritis and finding of intra-articular cavity puncture. For stage I, based on the principle of RICE (rest, ice, compression and elevation), 1.8 g of Xuefuda was medicated orally once per day, intravenous dripping of 250 mL of hemostasis mixture twice a day and 1.2 g of clindamycin per day were also given for hemostasis and anti-inflammation. For stage II-III, Kangyanling was additionally administered via intra-articular cavity injection twice a week, 2 mL every time, for 5-6 times in total. For stage IV, the drug for intra-articular cavity injection was replaced with 25 mg of sodium hyaluronate and the frequency of injection reduced to every two weeks, for 5-6 times in total. Coagulation factors III and IV as well as blood plasma were not given in the whole treatment course. Short-term therapeutic effects and adverse reaction in patients were evaluated, and the long-term effects were followed-up after patients left the hospital with 6-month consolidation therapy by Xuefuda.</p><p><b>RESULTS</b>After a 3-week treatment, 33 patients (82.5%) were completely remitted; 5 (12.5%) were partially remitted and 2 (5.0%) un-remitted, setting the short-term effective rate at 95.0% (38 cases). The 6-month follow-up showed that except for a relapse in 2 and 4 patients of stage III and IV respectively, long-term remission displayed in all the other 34 patients, with the remission sustaining rate being 85.0%. No complication such as an infection, bleeding or aggravating pain occurred in the 215 times intra-articular puncturing conducted in the 40 patients. Normal figures were shown in liver and kidney function, electrolytes, ECG, blood glucose and routine test of blood and urine throughout the course.</p><p><b>CONCLUSION</b>The graded treatment of integrative medicine for hemophilia with non-blood preparation has a favorable effect and is safe or without any adverse reaction, which opens a high efficacy and new safe path and thinking for the treatment of and deformity prevention in the hemophilic patients.</p>


Subject(s)
Adolescent , Adult , Child , Child, Preschool , Humans , Male , Acupuncture Therapy , Arthritis , Therapeutics , Combined Modality Therapy , Follow-Up Studies , Hemophilia A , Therapeutics , Medicine , Methods , Medicine, Chinese Traditional , Methods , Treatment Outcome , Western World
6.
Chinese journal of integrative medicine ; (12): 141-144, 2007.
Article in English | WPRIM | ID: wpr-282424

ABSTRACT

<p><b>OBJECTIVE</b>To observe the effect of Xueyou Mixture (, XYM) on blood coagulation factors and its safety in treating hemophilia.</p><p><b>METHODS</b>To the randomly selected 65 inpatients of hemophilia, XYM was administered accompanied with intravenous dripping of liver cell growth factor 60-100 mg once a day to protect the liver, with no blood products like concentrated VIII and FIX factors or blood plasma given. The treatment lasted for 3 weeks. The short-term efficacy and adverse reactions were observed. The long-term efficacy in patients was observed in a follow-up study of 6-12 months after they were discharged from the hospital but continuously took XYM orally.</p><p><b>RESULTS</b>The short-term markedly effective rate in the patients was 95.38% (62/65). After they were treated for 3 weeks, the level of FVIII factor activity increased in 56 patients of type A from (3.32+/-2.21) % to (4.18+/-2.23) %, and in 9 of type B from (4.92+/-1.81) % to (5.64+/-1.96) %. Compared with that before treatment, the difference was significant in both of them (P<0.01). No obvious adverse reaction was found in the treatment period. The follow-up study showed that in 22 patients of type A, the FVIII factor activity ratio increased from (3.25+/-2.11) % to (6.31+/-2.16) %, (8.36+/-1.05) %, and (16.38+/-2.71) % in the 2nd, 3rd and 6th month after discharge respectively, all showing significant difference to that before treatment (P<0.01); and in 4 patients of type B, it increased from (4.15+/-2.26) % to 7.8% and 11.6% (mean value) in the 2nd and 6th month respectively.</p><p><b>CONCLUSION</b>XYM could raise the activity of factors VIII and IX in patients with hemophilia, and the degree of the rise is related with the duration of the therapy, with no obvious adverse reaction, which strikes out a new path and new train of thinking for the treatment of the disease by nonblood preparation.</p>


Subject(s)
Adolescent , Adult , Child , Child, Preschool , Female , Humans , Infant , Male , Middle Aged , Blood Coagulation Factors , Drugs, Chinese Herbal , Therapeutic Uses , Follow-Up Studies , Hemoglobins , Hemophilia A , Blood , Drug Therapy , Medicine, Chinese Traditional
7.
Journal of Central South University(Medical Sciences) ; (12): 24-27, 2006.
Article in Chinese | WPRIM | ID: wpr-813774

ABSTRACT

OBJECTIVE@#To explore the effect of realgar on the gene expression profiles of multiple myeloma cell line RPMI 8226 by apply cDNA microarray.@*METHODS@#The gene expression of RPMI 8226 cells before and after 48 hours of realgar treatment was determined with a cDNA microarray representing 4096 human genes.@*RESULTS@#At the mRNA level, 164 genes were differentially altered; 53 genes were up-regulated; and 111 genes were down-regulated.@*CONCLUSION@#The realgar treatment to RPMI 8226 cell line may induce a number of gene changes. Many genes may be involved in the pathogenesis of multiple myeloma. BTG1, ALK1, and TXNIP genes may play an important role in the apoptosis and differentiation of RPMI 8226 cells.


Subject(s)
Humans , Arsenicals , Pharmacology , Gene Expression Profiling , Multiple Myeloma , Pathology , Oligonucleotide Array Sequence Analysis , Sulfides , Pharmacology , Tumor Cells, Cultured
8.
Journal of Experimental Hematology ; (6): 386-390, 2005.
Article in Chinese | WPRIM | ID: wpr-356553

ABSTRACT

To study the effect of realgar on expression of survivin in leukemia cell lines, HL-60 and Jurket cell lines were used as in vitro models. The expression of survivin was detected by Western blot analysis and immunofluorescence, and the expressions of Fas and caspase-3 were examined by immunohistochemistry. The results showed that the expression of survivin was positive in the two cell lines. HL-60 cells did not express Fas and caspase-3, and Jurket cells were Fas-positive and caspase-3 was negative. Realgar induced a dose- and time-dependent down-regulation of survivin expression in Jurket cells, and especially in HL-60. Caspase-3 expression changed from negative to positive in HL-60 cell, but there still was no expression in Jurket cell. It is concluded that survivin expression level decreased during leukemia cell apoptosis induced by Realgar. The down-regulation of survivin expression may be an important mechanism in leukemia cell apoptosis induced by realgar through mitochondrial pathway.


Subject(s)
Humans , Antineoplastic Agents , Pharmacology , Apoptosis , Arsenicals , Pharmacology , Blotting, Western , Caspase 3 , Metabolism , Dose-Response Relationship, Drug , Fluorescent Antibody Technique , HL-60 Cells , Immunohistochemistry , Inhibitor of Apoptosis Proteins , Jurkat Cells , Leukemia , Metabolism , Pathology , Microtubule-Associated Proteins , Neoplasm Proteins , Sulfides , Pharmacology , Time Factors , fas Receptor , Metabolism
9.
China Journal of Chinese Materia Medica ; (24): 553-556, 2003.
Article in Chinese | WPRIM | ID: wpr-282269

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of Realgar on procoagulant activity (PCA), tissue factor expression and tissue factor mRNA transcription in acute promyelocytic leukemia (APL) cell lines NB4 and MR2 cells.</p><p><b>METHOD</b>NB4 and MR2 cells were treated with 300 micrograms.L-1 Realgar PCA of the treated cells was detected using one-stage clotting assay. TF antigen was detected by ELISA and TFmRNA by semi-quantitive RT-PCR.</p><p><b>RESULT</b>The PCA and TF antigen level in NB4 and MR2 cells were significantly higher than that in HL-60 and K562 cells. Realgar could down-regulate the membrane PCA, TF antigen and TF mRNA transcription of NB4 and MR2 cells in a time-dependent manner.</p><p><b>CONCLUSION</b>Down-regulating TF expression and PCA of NB4 and MR2 cells by Realgar may be one of the mechanism of its improvement effect on DIC-related hemorrhage of APL patients.</p>


Subject(s)
Humans , Antineoplastic Agents , Pharmacology , Arsenicals , Pharmacology , Blood Coagulation Factors , Cysteine Endopeptidases , Metabolism , Drug Resistance, Neoplasm , Gene Expression Regulation, Leukemic , HL-60 Cells , K562 Cells , Leukemia, Promyelocytic, Acute , Metabolism , Pathology , Materia Medica , Pharmacology , Neoplasm Proteins , Metabolism , RNA, Messenger , Genetics , Sulfides , Pharmacology , Thromboplastin , Genetics , Tretinoin , Pharmacology
10.
China Journal of Chinese Materia Medica ; (24): 600-604, 2002.
Article in Chinese | WPRIM | ID: wpr-271863

ABSTRACT

<p><b>OBJECTIVE</b>To elucidate the molecular mechanism of realgar-induced apoptosis and differentiation of acute promyelocytic leukemia(APL) cell line NB4.</p><p><b>METHOD</b>The response of NB4 cells to realgar was explored with a cDNA microarray representing 1003 different human genes.</p><p><b>RESULT</b>The analysis of gene expression profiles indicated that 9 genes were up-regulated and 37 genes were down-regulated. Among the 9 up-regulated genes, 2 genes were involved in proteasome degradation pathway.</p><p><b>CONCLUSION</b>PSMC2, PSMD1 and ITGB1 genes may play a role in the apoptosis and differentiation of NB4 cells.</p>


Subject(s)
Humans , Antineoplastic Agents , Pharmacology , Arsenicals , Pharmacology , Gene Expression Profiling , Gene Expression Regulation , Genes, Neoplasm , Genetics , Leukemia, Promyelocytic, Acute , Genetics , Pathology , Materia Medica , Pharmacology , Oligonucleotide Array Sequence Analysis , Sulfides , Pharmacology , Tumor Cells, Cultured
11.
China Journal of Chinese Materia Medica ; (24): 211-215, 2002.
Article in Chinese | WPRIM | ID: wpr-274979

ABSTRACT

<p><b>OBJECTIVE</b>To acquire a deep understanding of the possible mechanisms of realgar in the treatment of acute promyelocytic leukemia (APL).</p><p><b>METHOD</b>All-trans retinoic acid (ATRA) resistant APL cell line MR2 was used as in vitro model. The effect of realgar on MR2 cell was observed by watching cell viability, cell growth, and by using Methy thiazolyl tetrazolium (MTT) assay, cell morphology, DNA gel electrophoresis and flow cytometry assay.</p><p><b>RESULT</b>The viability and growth of MR2 cell were inhibited after the treatment, to some extent, in a dose and time dependent manner. After being treated with realgar, MR2 cell presented morphologically some features of apoptotic cells such as intact cell membrane, chromatin condensation and nuclear fragmentation, and apoptotic body could be found by electron microscopy as well. Sub-G1 cells were observed by flow cytometry, as well as Annexin V FITC+/PI-cells. DNA ladder could be found by DNA gel electrophoresis.</p><p><b>CONCLUSION</b>Realgar can induce apoptosis of ATRA resistant APL cell line MR2, Which shows the therapeutic effect of realgar on APL may be different from that of ATRA.</p>


Subject(s)
Humans , Antineoplastic Agents , Pharmacology , Apoptosis , Arsenicals , Pharmacology , Cell Division , Cell Survival , Drug Resistance, Neoplasm , Leukemia, Promyelocytic, Acute , Pathology , Materia Medica , Pharmacology , Sulfides , Pharmacology , Tretinoin , Pharmacology , Tumor Cells, Cultured
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