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Métodos Terapéuticos y Terapias MTCI
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1.
Mol Med Rep ; 15(4): 2057-2066, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-28260045

RESUMEN

Doxorubicin (DOX) is an antineoplastic drug widely used for the treatment of various types of cancer; however, it can induce severe side effects, such as myelosuppression and cardiotoxicity. Sanyang Xuedai (SYKT) is a natural medicine originating from an ancient prescription of the Dai nationality in Southwest China. With eight Chinese herbal medicines, including sanguis draconis, radix et rhizoma notoginseng, radix et rhizoma glycyrrhizae and radix angelicae sinensis as the primary ingredients, SYKT has been reported to possess numerous biological functions. The present study investigated whether SYKT can confer protection against DOX­induced myelosuppression and cardiotoxicity, and explored the potential mechanism involved. Mice were treated with DOX, SYKT or a combination of the two; hematopoietic functions were assessed by measuring the number of peripheral blood cells, cluster of differentiation CD34+/CD44+ bone marrow cells and apoptotic cells. Myocardial enzymes, including aspartate aminotransferase, lactate dehydrogenase, creatine kinase (CK) and its isoform CK­MB, were assessed using a biochemical analyzer. The apoptotic rate of cardiomyocytes was assessed using flow cytometry. Histopathological analysis was conducted using hematoxylin­eosin staining. Intracellular reactive oxygen species (ROS) production was evaluated using a dichlorofluorescein intensity assay. The mice treated with DOX exhibited a reduced survival rate, reduced peripheral blood and CD34+/CD44+ cell counts, elevated myocardial enzymes and apoptotic indices in bone marrow cells and cardiomyocytes, all of which were effectively prevented by SYKT co­administration. Furthermore, bone marrow cells and myocytes from mice treated with DOX demonstrated increased dichlorofluorescein intensity, which was attenuated by SYKT. Notably, SYKT did not interfere with the effects of DOX on tumor volume or the induction of tumor cell apoptosis in tumor­bearing mice. The present study indicated that SYKT may counteract DOX­induced myelosuppression and cardiotoxicity through inhibiting ROS­mediated apoptosis. These findings suggested that SYKT may have potential as a means to counteract the potentially fatal hematopoietic and cardiac complications associated with DOX treatment.


Asunto(s)
Antibióticos Antineoplásicos/toxicidad , Apoptosis/efectos de los fármacos , Cardiotoxicidad/tratamiento farmacológico , Doxorrubicina/toxicidad , Medicamentos Herbarios Chinos/uso terapéutico , Hematopoyesis/efectos de los fármacos , Sustancias Protectoras/uso terapéutico , Animales , Antibióticos Antineoplásicos/uso terapéutico , Médula Ósea/efectos de los fármacos , Médula Ósea/patología , Cardiotoxicidad/metabolismo , Cardiotoxicidad/patología , Doxorrubicina/uso terapéutico , Femenino , Corazón/efectos de los fármacos , Ratones , Ratones Endogámicos C57BL , Miocardio/enzimología , Miocardio/patología , Neoplasias/tratamiento farmacológico , Especies Reactivas de Oxígeno/metabolismo
2.
BMC Bioinformatics ; 10 Suppl 1: S42, 2009 Jan 30.
Artículo en Inglés | MEDLINE | ID: mdl-19208144

RESUMEN

BACKGROUND: Intrinsically unstructured or disordered proteins are common and functionally important. Prediction of disordered regions in proteins can provide useful information for understanding protein function and for high-throughput determination of protein structures. RESULTS: In this paper, algorithms are presented to predict long and short disordered regions in proteins, namely the long disordered region prediction algorithm DRaai-L and the short disordered region prediction algorithm DRaai-S. These algorithms are developed based on the Random Forest machine learning model and the profiles of amino acid indices representing various physiochemical and biochemical properties of the 20 amino acids. CONCLUSION: Experiments on DisProt3.6 and CASP7 demonstrate that some sets of the amino acid indices have strong association with the ordered and disordered status of residues. Our algorithms based on the profiles of these amino acid indices as input features to predict disordered regions in proteins outperform that based on amino acid composition and reduced amino acid composition, and also outperform many existing algorithms. Our studies suggest that the profiles of amino acid indices combined with the Random Forest learning model is an important complementary method for pinpointing disordered regions in proteins.


Asunto(s)
Algoritmos , Aminoácidos/química , Inteligencia Artificial , Proteínas/química , Bases de Datos de Proteínas , Análisis de Secuencia de Proteína/métodos
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