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1.
Pak J Pharm Sci ; 35(1(Supplementary)): 219-225, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-35228180

RESUMEN

A polyphenolic flavone Luteolin (3',4',5,7-tetrahydroxyflavone) is found in various plants and is traditionally used in Chinese medicine. It is obtained from Alstonia scholaris (L.) R.Br Flower belonging to the family Apocynaceae while investigation. Various studies have been demonstrated the antioxidant or antiulcer potential of luteolin from different plant sources. In the present investigation the antioxidant or antiulcer effect of the Luteolin has been carried out using molecular docking simulations. The objective of this study was to analyze the antioxidant and antiulcer potential of luteolin obtained during isolation. The in vitro biological evaluation has been supported by the in silico studies using Autodock vina 4 shows the ligand-protein interaction of lute olin with 1HD2, 4GY7 and 3O1Q. Luteolin showed significant DPPH scavenging and urease inhibition activity i.e., 23.4 ± 0.87, 6.21±0.45 IC50 (uM) respectively as compared to the standard BHA and thiourea 44.2±0.45, 22.4±0.29 IC50 (uM) respectively. The docking simulations showed significant binding pocket sites with the respective proteins1HD2, 4GY7 and 3O1Q with the least binding energy -6.8, -8.0 and -8.2 kcal/mol respectively. Thus, Strong evidence has been presented with their confirmation structural interaction via molecular docking with proteins that serve as binding sites for available Luteolin molecule. The findings justify the application of the compound as a novel antioxidant and antiulcer agent.


Asunto(s)
Alstonia/química , Luteolina/farmacología , Fitoquímicos/farmacología , Ureasa/antagonistas & inhibidores , Compuestos de Bifenilo , Depuradores de Radicales Libres , Regulación de la Expresión Génica/efectos de los fármacos , Humanos , Luteolina/química , Modelos Moleculares , Simulación del Acoplamiento Molecular , Estructura Molecular , Peroxirredoxinas/genética , Peroxirredoxinas/metabolismo , Fitoquímicos/química , Picratos
2.
Pak J Pharm Sci ; 34(2(Supplementary)): 747-753, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-34275810

RESUMEN

Non-steroidal anti-inflammatory drugs (NSAIDs) are frequently used for the treatment and prevention of inflammation with the increase in number of side effects. Traditional plants have been used to treat inflammation owing to lesser adverse responses. Croton bonplandianus being an anti-inflammatory plant is extensively utilized all over the world. The methanolic and aqueous leaves extracts of Croton bonplandianus were exposed to anti-inflammatory activity in the carrageenan induced paw edema against standard diclofenac sodium, followed by the histopathlogical examination. The highest dose of methanolic extract were shown significant anti-inflammatory action having a significant P-value (P<0.05-0.001) compared with the diclofenac sodium (P<0.01-0.001) and aqueous extracts (P<0.5-0.01). The histopathological examination illustrated the vasodialation with reduction in the intensity of edema, neutrophils infiltration and other inflammatory cells. C. bonplandianus being a reactive oxygen species scavenger, responsible to exert an excellent anti-inflammatory activity. The present study confirmed the anti-inflammatory potential of drug extracts and authors recommended its utilization in the treatment of pain, inflammation and relevant diseases in future. However, phytochemical screening is to be required for the complete evaluation of active chemical constituent (s).


Asunto(s)
Antiinflamatorios/farmacología , Croton/química , Extractos Vegetales/farmacología , Hojas de la Planta/química , Animales , Croton/efectos adversos , Diclofenaco/farmacología , Modelos Animales de Enfermedad , Relación Dosis-Respuesta a Droga , Edema/tratamiento farmacológico , Edema/patología , Masculino , Hojas de la Planta/efectos adversos , Ratas , Ratas Wistar , Especies Reactivas de Oxígeno/metabolismo
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