Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
Añadir filtros








Intervalo de año
1.
Indian J Exp Biol ; 2013 Jun; 51(6): 464-469
Artículo en Inglés | IMSEAR | ID: sea-147615

RESUMEN

Diabetic nephropathy (DN) has a complex pathogenesis and poor prognosis due to the lack of therapeutic interventions. The present study investigates the effect of A. marmelos leaf extract (AME) on early alloxan induced DN. The treatment with AME was found to significantly decrease the fasting blood sugar, total cholesterol, blood urea, creatinine and renal TBARS and increased the levels of renal reduced glutathione and catalase significantly as compared to the diabetic control group. The maximum dose-dependent protection was observed at a dose of 200 mg kg-1. Histological examination revealed marked reversal of the morphological derangements with AME treatment as indicated by a decrease in glomerular expansion, tubular dilatation and inflammatory cells. The present results conclude that AME treatment has a significant ameliorative effect on early changes induced in the kidneys by alloxan and improves the outcome of DN.


Asunto(s)
Aegle/química , Aloxano , Animales , Glucemia/análisis , Catalasa/metabolismo , Diabetes Mellitus Experimental/tratamiento farmacológico , Nefropatías Diabéticas/inducido químicamente , Nefropatías Diabéticas/tratamiento farmacológico , Femenino , Glutatión/metabolismo , Hipoglucemiantes/farmacología , Riñón/efectos de los fármacos , Peroxidación de Lípido/efectos de los fármacos , Masculino , Fitoterapia , Extractos Vegetales/farmacología , Hojas de la Planta/química , Ratas , Ratas Wistar , Sustancias Reactivas al Ácido Tiobarbitúrico/metabolismo
2.
Indian J Exp Biol ; 2013 Feb; 51(2): 157-164
Artículo en Inglés | IMSEAR | ID: sea-147579

RESUMEN

Graded doses of 50% ethanolic extract of dried fruit pulp of Aegle marmelos (AME) (100, 200 and 400 mg/kg) daily for 14 days in acetic acid (AA)-induced colitis in rats showed 200 mg/kg of AME as an optimal effective dose against AA-induced colonic damage score and weight. This dose (200 mg/kg; po) was further studied in AA-induced colitis for its effects on various physical (mucous/blood in stool, food and water intake and body weight changes), histology, antibacterial activity and biochemical parameters like free radicals (nitric oxide and lipid peroxidation), antioxidants (superoxide dismutase, catalase and reduced glutathione) and myeloperoxidase (acute-inflammatory marker) activities in rat colonic tissue. AME decreased colonic mucosal damage and inflammation (macroscopic and microscopic), mucous/bloody diarrhea, fecal frequency and increased body weight affected in AA-induced colitis. AME showed significant antibacterial activity and enhanced the antioxidants but decreased free radicals and myeloperoxidase activities thereby decreasing tissue damage and inflammation and thus, affording ulcer healing. The above effects of A. marmelos authenticated its use in indigenous system of Medicine.


Asunto(s)
Aegle/química , Animales , Antibacterianos/farmacología , Antioxidantes/metabolismo , Bacterias/efectos de los fármacos , Peso Corporal/efectos de los fármacos , Colitis/tratamiento farmacológico , Colitis/patología , Colon/efectos de los fármacos , Colon/patología , Conducta de Ingestión de Líquido/efectos de los fármacos , Conducta Alimentaria/efectos de los fármacos , Femenino , Radicales Libres/metabolismo , Frutas/química , Masculino , Pruebas de Sensibilidad Microbiana , Fitoterapia , Extractos Vegetales/farmacología , Extractos Vegetales/uso terapéutico , Ratas , Cicatrización de Heridas/efectos de los fármacos
3.
Pakistan Journal of Pharmaceutical Sciences. 2011; 24 (4): 427-433
en Inglés | IMEMR | ID: emr-137540

RESUMEN

Marmin or 7-[6', 7'-dihydroxygeranyl-oxy] coumarin is a compound isolated from Aegle marmelos Correa. In the study, we examined the effects of marmin on the contraction of guinea pig-isolated trachea stimulated by several inducers, namely histamine, metacholine, compound 48/80. We also evaluated its action against contraction induced by extracellular or intracellular calcium ion. The possibility of marmin to potentiate the


elaxation effect of isoprenaline was also studied. Marmin added in the organ bath at 10 min prior to the agonist inhibited the contraction elicited by histamine and metacholine in a concentration-dependent manner. Moreover, marmin antagonized the histamine-induced contraction in competitive manner. Marmin mildly potentiated the relaxation effect of isoprenaline. In the study, marmin abrogated the contraction of tracheal smooth muscle induced by compound 48/80, an inducer of histamine release. Besides, marmin successfully inhibited CaCl[2-]-induced contraction in Ca[2+] -free Krebs solution. Marmin also inhibited two phases of contraction which were consecutively induced by metacholine and CaCl[2] in Ca[2+]-free Krebs solution. Based on the results we concluded that marmin could inhibit contraction of the guinea-pig tracheal smooth muscle, especially by interfering histamine receptor, inhibiting the histamine release from mast, inhibiting intracellular Ca[2+] release from the intracellular store and the Ca[2+] influx through voltage-dependent Ca[2+] channels


Asunto(s)
Animales de Laboratorio , Masculino , Aegle/química , Cumarinas/aislamiento & purificación , Tráquea/efectos de los fármacos , p-Metoxi-N-metilfenetilamina/farmacología , Músculo Liso/efectos de los fármacos , Relajación Muscular/efectos de los fármacos , Contracción Muscular/efectos de los fármacos , Cobayas
4.
Indian J Exp Biol ; 2009 Mar; 47(3): 182-5
Artículo en Inglés | IMSEAR | ID: sea-63244

RESUMEN

Lipid lowering effect of 50% ethanolic extract of the leaves of A. marmelos (Linn.) was evaluated in triton and diet induced hyperlipidaemic models of Wistar albino rats. The extract at 125 and 250 mg/kg dose levels inhibited the elevation in serum cholesterol and triglycerides levels on Triton WR 1339 administration in rats. The extract at the same dose levels significantly attenuated the elevated serum total cholesterol and triglycerides with an increase in the high-density lipoprotein cholesterol in high-fat diet- induced hyperlipidaemic rats. The standard drugs atorvastatin in the former and gemfibrozil in the latter studies showed slightly better effects.


Asunto(s)
Aegle/química , Animales , Aterosclerosis/prevención & control , Colesterol/sangre , Dieta Aterogénica , Modelos Animales de Enfermedad , Etanol , Hiperlipidemias/tratamiento farmacológico , Hipolipemiantes/uso terapéutico , Lipoproteínas HDL/sangre , Masculino , Extractos Vegetales , Triglicéridos/sangre , Animales , Antihipertensivos/farmacología , Aterosclerosis , Dieta Aterogénica , Femenino , Ajo/química
5.
Artículo en Inglés | IMSEAR | ID: sea-23532

RESUMEN

BACKGROUND & OBJECTIVE: Disease burden due to lymphatic filariasis is disproportionately high despite mass drug administration with conventional drugs. Usage of herbal drugs in traditional medicine is quite well known but largely empirical. Hence the present study was designed to screen the in vitro antifilarial effect of four herbal plants on Brugia malayi. METHODS: Motility of microfilariae of B. malayi after incubation for 48 h with aqueous/methanol extracts of Vitex negundo L. (roots), Butea monosperma L. (roots and leaves), Ricinus communis L. (leaves), and Aegle marmelos Corr. (leaves) was explored in the concentration range of 20 to 100 ng/ml for possible antifilarial effect by comparing with suitable solvent control. RESULTS: Butea monosperma leaves and roots, Vitex negundo root and Aegle marmelo leaves showed significant inhibition of motility of microfilariae as compared to controls whereas inhibitory activity demonstrated by Ricinus communis L. leaves was not significant. Antifilarial effects imparted by all these extracts were found to be a function of their relative concentrations. Inhibitory concentrations (IC(50)) for the plant extracts with significant antifilarial activity against Brugia malayi microfilariae in in vitro system have been derived to be 82, 83 and 70 ng/ml for Vitex negundo L., Butea monosperma L. and Aegle marmelos Corr. respectively. INTERPRETATION & CONCLUSION: The present study recorded significant antifilarial effect of all plant extracts studied except for Ricinus communis L. leaves and contributes to the development of database for novel drug candidates for human lymphatic filariasis.


Asunto(s)
Aegle/química , Animales , Brugia Malayi/efectos de los fármacos , Butea/química , Movimiento Celular/efectos de los fármacos , Filariasis/tratamiento farmacológico , Humanos , Microfilarias/efectos de los fármacos , Preparaciones de Plantas/farmacología , Ricinus/química , Vitex/química
6.
Indian J Physiol Pharmacol ; 2004 Jan; 48(1): 81-8
Artículo en Inglés | IMSEAR | ID: sea-107927

RESUMEN

Oxidative stress induced by alloxan has been shown to damage pancreatic beta-cell and produce hyperglycemia in rats. Aegle marmelos leaf extract is being used in Ayurveda as a medicine for diabetes. The present study examined the action of Aegle marmelos against experimental diabetes as well as the antioxidant potential of the drug. A methanolic extract of Aegle marmelos was found to reduce blood sugar in alloxan diabetic rats. Reduction in blood sugar could be seen from 6th day after continuous administration of the extract and on 12th day sugar levels were found to be reduced by 54%. Oxidative stress produced by alloxan was found to be significantly lowered by the administration of Aegle marmelos extract. This was evident from a significant decrease in lipid peroxidation, conjugated diene and hydroperoxide levels in serum as well as in liver induced by alloxan. Catalase and glutathione peroxidase activity in blood and liver were found to be increased from 9th day onwards after drug administration. Superoxide dismutase and glutathione levels were found to be increased only on 12th day. These results indicate that Aegle marmelos extract effectively reduced the oxidative stress induced by alloxan and produced a reduction in blood sugar.


Asunto(s)
Aegle/química , Animales , Antioxidantes/farmacología , Glucemia/metabolismo , Catalasa/sangre , Diabetes Mellitus Experimental/sangre , Glutatión/sangre , Peróxido de Hidrógeno/sangre , Hipoglucemiantes/farmacología , Peroxidación de Lípido/efectos de los fármacos , Masculino , Oxidantes/metabolismo , Estrés Oxidativo/efectos de los fármacos , Extractos Vegetales/farmacología , Hojas de la Planta/química , Ratas , Ratas Wistar , Superóxido Dismutasa/sangre
7.
Indian J Exp Biol ; 2003 Nov; 41(11): 1285-8
Artículo en Inglés | IMSEAR | ID: sea-60369

RESUMEN

A study was undertaken to evaluate the anti-lipid peroxidative activity of an aqueous extract of A. marmelos fruits (AMFEt) in streptozotocin diabetic rats in heart and pancreas. Oral administration of AMFEt for 30 days (125 and 250 mg kg(-1) body weight twice daily) produced a significant decrease in the elevated levels of peroxidation products, viz. thiobarbituric acid reactive substances and hydroperoxides in the tissues of diabetic rats. The depressed activities of superoxide dismutase, catalase and glutathione peroxidase and lowered glutathione content in the heart and pancreas of diabetic rats were found to increase on treatment with AMFEt. AMFEt at a dose of 250 mg kg(-1) was more effective than glibenclamide (300 microg kg(-1)) and both reversed all the values significantly. Thus AMFEt exhibits anti-oxidative activity in streptozotocin diabetic rats.


Asunto(s)
Administración Oral , Aegle/química , Animales , Antioxidantes/uso terapéutico , Glucemia/metabolismo , Catalasa/metabolismo , Diabetes Mellitus Experimental/tratamiento farmacológico , Femenino , Glutatión/metabolismo , Glutatión Peroxidasa/metabolismo , Gliburida/uso terapéutico , Corazón/efectos de los fármacos , Peróxido de Hidrógeno/metabolismo , Hipoglucemiantes/uso terapéutico , Peroxidación de Lípido/efectos de los fármacos , Páncreas/efectos de los fármacos , Fitoterapia , Extractos Vegetales/uso terapéutico , Ratas , Ratas Wistar , Estreptozocina/toxicidad , Superóxido Dismutasa/metabolismo , Sustancias Reactivas al Ácido Tiobarbitúrico/metabolismo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA