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1.
Phytochemistry ; 156: 135-141, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-30292877

RESUMO

Viola odorata L. (Violaceae), an Indian medicinal plant, contains a plethora of cyclotides, which are a class of cyclic peptides derived from plants, possessing several applications. Somatic embryo culture of V. odorata was developed, via indirect somatic embryogenesis, to serve as an alternative to natural plant biomass for sustainable and continuous production of its bioactive ingredients, such as cyclotides. Among the various combinations of phytohormones tested, Murashige and Skoog medium supplemented with 1 mg/l thidiazuron gave rise to the maximum frequency of induction (86.7%) and a high number of somatic embryos (3) from an embryogenic callus. Identification and characterization of cyclotides in the somatic embryos were carried out using a Fourier transform mass spectrometer coupled with liquid chromatography (LC-FTMS). Among the cyclotides identified in the study, few were found to be exclusively present in the somatic embryo culture. Furthermore, the relative abundance of the cyclotides was higher in somatic embryo extract than in the natural plant extract. The biological activities (cytotoxic, haemolytic and antimicrobial) of the somatic embryos and the parent plant were compared. Unlike the natural plants, the somatic embryo extracts demonstrated specificity i.e. they were found to be potent against cancerous cells but not against non-cancerous cell line or red blood cells. In contrast to the plant extract, the somatic embryos extracts were found to be potent against Escherichia coli and Staphylococcus aureus. These results suggest that somatic embryos of V. odorata (rich in cyclotides) can be used as an alternative to plant biomass for its therapeutic applications and germplasm conservation.


Assuntos
Antibacterianos/farmacologia , Antineoplásicos Fitogênicos/farmacologia , Ciclotídeos/farmacologia , Extratos Vegetais/farmacologia , Viola/metabolismo , Antibacterianos/biossíntese , Antibacterianos/química , Antineoplásicos Fitogênicos/biossíntese , Antineoplásicos Fitogênicos/química , Linhagem Celular Tumoral , Proliferação de Células/efeitos dos fármacos , Ciclotídeos/biossíntese , Ciclotídeos/química , Relação Dose-Resposta a Droga , Ensaios de Seleção de Medicamentos Antitumorais , Escherichia coli/efeitos dos fármacos , Células HEK293 , Humanos , Testes de Sensibilidade Microbiana , Extratos Vegetais/biossíntese , Extratos Vegetais/química , Pseudomonas aeruginosa/efeitos dos fármacos , Staphylococcus aureus/efeitos dos fármacos , Relação Estrutura-Atividade , Viola/química , Viola/embriologia
2.
Exp Eye Res ; 128: 73-82, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25257692

RESUMO

This study investigated the potential of vitamin K1 against streptozotocin-induced diabetic cataract in Wistar rats. A single, intraperitoneal injection of streptozotocin (STZ) (35 mg/kg) resulted in hyperglycemia, accumulation of sorbitol and formation of advanced glycation end product (AGE) in eye lens. Hyperglycemia in lens also resulted in superoxide anion and hydroxyl radical generation and less reduced glutathione suggesting oxidative stress in lens. Hyperglycemia also resulted in increase in lens Ca2+ and significant inhibition of lens Ca2+ ATPase activity. These changes were associated with cataract formation in diabetic animals. By contrast treatment of diabetic rats with vitamin K1 (5 mg/kg, sc, twice a week) resulted in animals with partially elevated blood glucose and with transparent lenses having normal levels of sorbitol, AGE, Ca2+ ATPase, Ca2+, and oxidative stress. Vitamin K 1 may function to protect against cataract formation in the STZ induced diabetic rat by affecting the homeostasis of blood glucose and minimizing subsequent oxidative and osmotic stress. Thus, these results show that Vitamin K1 inhibits diabetic-cataract by modulating lens Ca2+ homeostasis and its hypoglycemic effect through its direct action on the pancreas.


Assuntos
Cálcio/metabolismo , Catarata/prevenção & controle , Diabetes Mellitus Experimental/prevenção & controle , Homeostase/fisiologia , Hiperglicemia/metabolismo , Cristalino/metabolismo , Vitamina K 1/uso terapêutico , Vitaminas/uso terapêutico , Animais , Glicemia/metabolismo , ATPases Transportadoras de Cálcio/metabolismo , Catarata/metabolismo , Diabetes Mellitus Experimental/metabolismo , Glutationa/metabolismo , Produtos Finais de Glicação Avançada/metabolismo , Radical Hidroxila/metabolismo , Masculino , Estresse Oxidativo , Ratos , Ratos Wistar , Sorbitol/metabolismo , Superóxidos/metabolismo
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