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1.
Chem Pharm Bull (Tokyo) ; 58(6): 840-2, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20522996

ABSTRACT

Three new 4-hydroxyisoflavans, named lyratin A (1), lyratin B (2) and lyratin C (3), along with a known compound, 4,7,2'trihydroxy-4'-methoxyisoflavan (4), were isolated from the whole plant of Solanum lyratum. Their structures were established by means of detailed physical data analyses. In vitro, four compounds showed anti-inflammatory activities with inhibitory ratios of release of beta-glucuronidase from polymorphonuclear leukocytes of rats in the range of 30.3-38.6% at 10 microM.


Subject(s)
Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/pharmacology , Isoflavones/chemistry , Isoflavones/pharmacology , Neutrophils/drug effects , Solanum/chemistry , Animals , Anti-Inflammatory Agents/isolation & purification , Neutrophils/immunology , Rats
2.
Zhongguo Zhong Yao Za Zhi ; 32(18): 1906-8, 2007 Sep.
Article in Chinese | MEDLINE | ID: mdl-18051904

ABSTRACT

OBJECTIVE: To observe the effect on P170, LRP, TOPO II of S180 tumour MDR mice for matter by 70% ethanol with Huanglian Jiedu Tang, and then discuss the molecular biology base for clinic. METHOD: 18-22 gramme mice were divided into four groups for normal S180 tumour cell group, matter by 70% ethanol with Huanglian Jiede Tang 100 mg x kg(-1) and 50 mg x kg(-1) in random. Each mouse was given S180 cell 0.2 mL by celiac, and after 24 hours give cisplatin for Injective 3 mg x kg(-1), ip, once a week. And give cyclophosphamide and 5-FU 3 mg x kg(-1), ig, once every day. After 15 days, collect lively mice ascites and give it for onefold normal mice. And then repeat before process. At the same time, every group was given corresponding medicine for 0.2 mL x 10 g(-1). The normal group and the model group were given the same cubage water, all together fore weeks. At last observd the P170, LRP, TOPO II by flow cytometry. RESULT: Matter by 70% ethanol with Huanglian Jiedu Tang could obviously reduce the express of P170 and LRP, and the activiation of TOPO II. CONCLUSION: Matter by 70% ethanol with Huanglian Jiedu Tang can intervene the ocurrence of the multi-drug resistance of tumour cells by regulating the biology gene.


Subject(s)
Drug Resistance, Multiple/drug effects , Drug Resistance, Neoplasm/drug effects , Drugs, Chinese Herbal/pharmacology , Sarcoma 180/prevention & control , ATP Binding Cassette Transporter, Subfamily B, Member 1/metabolism , Animals , Cell Line, Tumor , Coptis/chemistry , DNA Topoisomerases, Type II/metabolism , Drug Combinations , Drugs, Chinese Herbal/chemistry , Drugs, Chinese Herbal/isolation & purification , Ethanol/chemistry , Flow Cytometry , Mice , Phytotherapy , Plants, Medicinal/chemistry , Sarcoma 180/metabolism , Sarcoma 180/pathology , Vault Ribonucleoprotein Particles/metabolism
3.
Zhong Yao Cai ; 29(1): 40-2, 2006 Jan.
Article in Chinese | MEDLINE | ID: mdl-16722318

ABSTRACT

OBJECTIVE: To Observe the effect caused by matrine's used on the reversion of obtained multi-drug resistance of mice S180's tumour cell induced by chemotherapy of Cisplatin + 5-FU + Cytoxan (PFC) and discuss its molecular mechanism. METHODS: Patterned the methods of PFC chemotherapy in clinic, the mice were given Cisplatim 3 mg/kg x ip once a week and Cytoxan, CTX and 5-FU 3 mg/kg x ip once everyday for 4 weeks to set up the mice models of multi-drug resistance of S180 tumor cell. At the same time, gave the mice models matrine 4 weeks, and observed the P170, LRP, TOPO II by flow cytometry. RESULTS: matrine could obviously reduce the express of P170, LRP and the activiation of TOPO II, correlated with mulit-drug resistance tumour cells which were induced by chemotherapy. CONCLUSION: Matrine, with its adjustment of correlated biotic active matter, can intervene the ocurrence of the multidrug resistance of tumor cells induced by chemotherapy.


Subject(s)
Alkaloids/pharmacology , Antineoplastic Agents, Phytogenic/pharmacology , Drug Resistance, Multiple/drug effects , Quinolizines/pharmacology , Sarcoma 180/metabolism , ATP Binding Cassette Transporter, Subfamily B, Member 1/biosynthesis , ATP Binding Cassette Transporter, Subfamily B, Member 1/genetics , Alkaloids/administration & dosage , Animals , Antineoplastic Combined Chemotherapy Protocols/pharmacology , Cisplatin/administration & dosage , Cyclophosphamide/administration & dosage , DNA Topoisomerases, Type II/biosynthesis , DNA Topoisomerases, Type II/genetics , Flow Cytometry , Fluorouracil/administration & dosage , Mice , Neoplasm Proteins/genetics , Neoplasm Proteins/metabolism , Quinolizines/administration & dosage , Sarcoma 180/pathology , Vault Ribonucleoprotein Particles/genetics , Vault Ribonucleoprotein Particles/metabolism , Matrines
4.
Zhongguo Zhong Yao Za Zhi ; 30(16): 1280-2, 2005 Aug.
Article in Chinese | MEDLINE | ID: mdl-16245910

ABSTRACT

OBJECTIVE: To observe the effect of tetrandrine on the P170 production expressed by multi-drug resistance gene, lung resistant protein (LRP), and topoisomeras II and elucidate the underlying molecular mechanism. METHOD: Cellular model of multi-drug resistance was established in S180 tumor cell by means of the scheme of PFC chemotherapy at the dosage lower than that with curative effect. P170, LRP and TOPO II were measured by flow cytometry after the mouse model was treated with tetrandrine for 4 weeks. RESULT: tetrandrine obviously reduced the enhancement of express of P170, LRP and the activity of TOPO II in the tumor cells with multi-drug resistance induced by chemotherapy. CONCLUSION: Tetrandrine significantly inhibits the multi-drug resistance of tumor cells induced by chemotherapy via diminishing both the expression of multi-drug resistance gene and the activity of topoisomeras II.


Subject(s)
ATP Binding Cassette Transporter, Subfamily B, Member 1/metabolism , Alkaloids/pharmacology , Benzylisoquinolines/pharmacology , DNA Topoisomerases, Type II/metabolism , Sarcoma 180/metabolism , Vault Ribonucleoprotein Particles/metabolism , Animals , Drug Resistance, Multiple , Drug Resistance, Neoplasm , Drugs, Chinese Herbal/pharmacology , Gene Expression Regulation, Neoplastic , Genes, MDR , Mice , Random Allocation , Sarcoma 180/enzymology , Sarcoma 180/pathology
5.
Zhongguo Zhong Yao Za Zhi ; 30(4): 280-3, 2005 Feb.
Article in Chinese | MEDLINE | ID: mdl-15724407

ABSTRACT

OBJECTIVE: To observe the effect of tetrandrine on reversion of mice S180's obtained multi-drug resistance tumor cell induced by chemotherapy by PFC. And then discuss the molecular mechanism of it for the use of TCM in clinic to restrain the drug-resistant of chemotherapy, thereby improve the curative effect. METHOD: By the methods of less dosage of chemotherapy PFC, give the mouse cisplatin 3 mg x kg(-1) i.p., once a week; CTX and 5-FU 3 mg x kg(-1) i.g. four weeks, set up the mice models of multi-drug resistance of S180 tumor cell, and then observe the P170, Fas, CD54 and apoposis by flow cytometry. RESULT: Tetrandrine can obviously lower the express of P170 increase the express of Fas and the apoposis of drug resistant tumor cell. And at the same time it can obviously reduce the express of intercellular adhesion molecule (CD54). CONCLUSION: Terandrine, with its adjustment of correlated biotic active matter, can intervene the occurrence of the multi-drug resistance of tumor cells induced by chemotherapy.


Subject(s)
Alkaloids/pharmacology , Apoptosis/drug effects , Benzylisoquinolines/pharmacology , Drug Resistance, Multiple/drug effects , Drug Resistance, Neoplasm/drug effects , Glycoproteins/metabolism , Sarcoma 180/pathology , ATP Binding Cassette Transporter, Subfamily B , Animals , Antineoplastic Agents, Phytogenic/pharmacology , Antineoplastic Combined Chemotherapy Protocols/pharmacology , Apoptosis Regulatory Proteins , Intercellular Adhesion Molecule-1/metabolism , Membrane Glycoproteins/metabolism , Mice , Sarcoma 180/metabolism , TNF-Related Apoptosis-Inducing Ligand , Tumor Cells, Cultured , Tumor Necrosis Factor-alpha/metabolism , fas Receptor/metabolism
6.
Zhongguo Zhong Yao Za Zhi ; 30(23): 1844-8, 2005 Dec.
Article in Chinese | MEDLINE | ID: mdl-16499024

ABSTRACT

OBJECTIVE: To observe the base of the interference in correlated biotic active matter obtained multi-drug resistance induced by chemotherapy for different alkaloid, and to supervise the use in clinic to restrain the multi-drug resistant of chemotherapy, and thereby to improve the curative effect. METHOD: After bestowing subter-dosage unite chemotherapeutant to ascites S180 mouse to set up the mouse models of multi-drug resistance of S180 tumour cell, and giving the mouse matrine, terandrine, oxymatrine and berberine hydrooh loride for 4 weeks, the P170, LRP, TOPOII, Fas and apoposis were determined by flow cytometry. RESULT: Matrine and terandrine could obviously reduce the express of P170, LRP and the activation of TOPOII, and increase the ratio of the express of Fas and the apoposis of drug resistant tumour cell. And at the same time it could obviously reduce the express of intercellular adhesion molecule(CD54). CONCLUSION: Matrine and terandrine can interfere in MDR which results from chemotherapeutics by the adjustment of correlated biotic active matter, besides, the different degree of alkaloid effect with different configuration.


Subject(s)
ATP Binding Cassette Transporter, Subfamily B, Member 1/metabolism , Alkaloids/pharmacology , Benzylisoquinolines/pharmacology , Drug Resistance, Multiple , Drug Resistance, Neoplasm , Quinolizines/pharmacology , Sarcoma 180/pathology , Alkaloids/isolation & purification , Animals , Apoptosis/drug effects , Benzylisoquinolines/isolation & purification , Berberine Alkaloids/isolation & purification , Berberine Alkaloids/pharmacology , DNA Topoisomerases, Type II/metabolism , Female , Male , Mice , Plants, Medicinal/chemistry , Quinolizines/isolation & purification , Random Allocation , Sarcoma 180/metabolism , Tumor Cells, Cultured , Vault Ribonucleoprotein Particles/metabolism , fas Receptor/metabolism , Matrines
7.
Huan Jing Ke Xue ; 25(2): 61-6, 2004 Mar.
Article in Chinese | MEDLINE | ID: mdl-15202236

ABSTRACT

As a whole of water column, suspended matter and surface sediment in the mainstream and the branch taking up industry wastewater, speciation and distribution characters of rare earth elements (REEs) were investigated systemically in the Baotou section of the Yellow River. This study shows that rare earth elements in the mainstream of the Baotou section of the Yellow River mainly exist in suspended particles, and the dissolved contents are in extremely minute quantities. REEs mainly exist in dissolved particles in the branch taking up industry wastewater, and suspended sigma REE and dissolved sigma REE are obviously higher than those in the mainstream. The change of sigma REE of dissolved particles in water phase along the Baotou section of the Yellow River is very similar to that of sigma REE of suspended particles, and consistent along the main river, it is that sigma REE increase appreciably from the control profile to the keystone discharged section, come to a head in the D site and reduce in the E site. This distribution pattern indicates pile industry wastewater of Baotou to rare earth elements in the mainstream of the Yellow River, particularly LREE. The REE distribution in the mainstream of the Baotou section of the Yellow River is the same, with LREE enrichment and Eu depletion. But LREE origin of D site is different from the other sites by excursion of LREE distribution curve and other geochemical parameters, they are origin of industry wastewater piled, otherwise the other four sites are origin of loess altiplano. And HREE are origin of loess altiplano in all the sites. The speciation characteristics of REE in the sediments and suspended matter are quite similar with the amount in as follows: residual >> bound to carbonates, bound to Fe-Mn oxides > bound to organic matter >> exchangeable. REEs exchangeable in surface sediment and suspended matter in the branch taking up industry wastewater are higher than those in the mainstream, it confirms that REEs in the mainstream mainly exist in suspended particles, and mainly exist in dissolved particles in the branch.


Subject(s)
Metals, Rare Earth/analysis , Rivers/chemistry , Water Pollutants, Chemical/analysis , Geologic Sediments/analysis
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