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2.
Indian J Physiol Pharmacol ; 44(2): 173-8, 2000 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-10846631

RESUMEN

Electroencephalographic patterns were studied in 30 normal healthy individuals practicing meditation and compared with 10 normal healthy controls not practicing meditation. In this study, we found prominent alpha wave activity and increase it its voltage in meditators as compared to controls. Meditators had significantly more alpha rhythm as compared to control group. Percentage of alpha waves were higher in persons performing meditation with good coherence which suggested good homogenicity, uniformity and increased orderliness of brain.


Asunto(s)
Electroencefalografía , Meditación , Adolescente , Adulto , Anciano , Ritmo alfa , Femenino , Lateralidad Funcional/fisiología , Hemodinámica/fisiología , Humanos , Masculino , Persona de Mediana Edad , Estimulación Luminosa , Pulso Arterial , Mecánica Respiratoria/fisiología
3.
J Nat Prod ; 61(4): 440-5, 1998 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-9584398

RESUMEN

Four new oleanane-type triterpene glycosides, proceraosides A-D (1-4), were isolated from the seeds of Albizia procera. Their structures were established by extensive NMR experiments and chemical methods. Compounds 1-3 comprised acacic acid as the aglycon and a monoterpenic carboxylic acid linked to a monoterpene quinovoside as the acyl moiety at C-21. The common oligosaccharide moiety linked to C-28 in 1-3 was determined as alpha-l-arabino- furanosyl-(1-->4)-[beta-D-glucopyranosyl-(1-->3)]-alpha-L-rhamnopyranosy l- (1-->2)-beta-D-glucopyranosyl ester. These compounds differed in the C-3-linked sugar unit or in the configuration of C-6' of the inner monoterpene moiety in the C-21-linked acyl unit. Compound 4 was established as the 16-deoxy analogue of 1.


Asunto(s)
Plantas Medicinales/química , Saponinas/aislamiento & purificación , Triterpenos/aislamiento & purificación , Secuencia de Carbohidratos , Espectroscopía de Resonancia Magnética , Espectrometría de Masas , Datos de Secuencia Molecular , Saponinas/farmacología , Semillas/química , Espectrometría de Masa Bombardeada por Átomos Veloces , Espectrofotometría Infrarroja , Espectrofotometría Ultravioleta , Triterpenos/farmacología
4.
J Nat Prod ; 60(12): 1269-74, 1997 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-9428160

RESUMEN

Four new oleanane-type triterpene glycosides, pithedulosides H-K (1-4), were isolated from the seeds of Pithecellobium dulce. Their structures were established by extensive NMR experiments and chemical methods. Compounds 1-3 comprised acacic acid as the aglycon and either monoterpene carboxylic acid and its xyloside or monoterpene carboxylic acid as the acyl moiety at C-21. The oligosaccharide moieties linked to C-3 and C-28 were determined as alpha-L-arabinopyranosyl-(1-->2)-alpha-L-arabinopyranosyl-(1 -->6)- [beta-D-glucopyranosyl-(1-->2)]-beta-D-glucopyranosyl and alpha-L-arabinofuranosyl-(1-->4)-[beta-D-glucopyranosyl-(1-->3)]-alpha- rhamnopyranosyl-(1-->2)-beta-D-glucopyranosyl ester, respectively. Compound 4 was established as an echinocystic acid 3-O-glycoside having the same sugar sequences as 1-3. Also obtained in this investigation was the known compound 5, which was identified as echinocystic acid 3-O-beta-D-xylopyranosyl- (1-->2)-alpha-L-arabinopyranosyl-(1-->6)-[beta-D-glucopyranosyl-(1 -->2)]- beta-D-glucopyranoside.


Asunto(s)
Plantas Medicinales/química , Saponinas/química , Triterpenos/química , Secuencia de Carbohidratos , Hidrólisis , India , Espectroscopía de Resonancia Magnética , Datos de Secuencia Molecular , Saponinas/aislamiento & purificación , Semillas/química , Espectrometría de Masa Bombardeada por Átomos Veloces , Triterpenos/aislamiento & purificación
5.
Phytochemistry ; 41(3): 887-93, 1996 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-8835462

RESUMEN

Six saponins were isolated from the seed kernel of Mimusops elengi, M. hexandra and M. manilkara. Their structures were determined using a combination of 1H NMR, 13C NMR and mass spectroscopy. Three of them are new compounds: 3-O-(beta-D-glucuronopyranosyl) 28-O-(alpha-L-rhamnopyranosyl (1-->3) beta-D-xylopyranosyl(1-->4) [alpha-L-rhamnopyranosyl(1-->3)] alpha-L-rhamnopyranosyl(1-->2) alpha-L-arabinopyranosyl) protobassic acid, 3-O-(beta-D-glucuronopyranosly) 28-O-(alpha-L-rhamnopyranosyl(1-->3) beta-D-xylopyranosyl(1-->4) alpha-L-rhamnopyranosyl(1-->2) alpha-L-arabinopyranosyl) 16-alpha-hydroxyprotobassic acid and 3-O-(beta-D-glucopyranosyl(1-->3) beta-D-glucopyranosyl) 28-O-(alpha-L-rhamnopyranosyl(1-->3) beta-D-xylopyranosyl(1-->4) alpha-L-rhamnopyranosyl(1-->2) alpha-L-arabinopyranosyl) protobassic acid.


Asunto(s)
Plantas Medicinales/química , Saponinas/aislamiento & purificación , Secuencia de Carbohidratos , Espectroscopía de Resonancia Magnética , Datos de Secuencia Molecular , Saponinas/química , Espectrometría de Masa Bombardeada por Átomos Veloces
6.
Planta Med ; 59(3): 215-7, 1993 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-8316589

RESUMEN

The antiulcer effect of aqueous extracts of the leaves of the neem tree was investigated in rats exposed to 2-h cold-restraint stress or given ethanol orally for 1 h. Extracts were administered in doses of 10, 40, or 160 mg leaf/kg body weight, either as single- or five-dose pretreatment regimens. Neem dose-dependently reduced gastric ulcer severity in rats subjected to stress and also decreased ethanol provoked gastric mucosal damage. The extract appeared to prevent mast cell degranulation and to increase the amount of adherent gastric mucus in stressed animals. These effects may explain, at least in part, the mode of the antiulcer action of neem.


Asunto(s)
Antiulcerosos/farmacología , Plantas Medicinales/química , Animales , Antiulcerosos/aislamiento & purificación , Femenino , Mucosa Gástrica/efectos de los fármacos , Mastocitos/efectos de los fármacos , Ratas , Ratas Sprague-Dawley , Árboles
7.
Planta Med ; 57(2): 122-4, 1991 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-17226137

RESUMEN

The 40-day-old IN VITRO proliferating shoots of ROSMARINUS OFFICINALIS L. var. GENUINA forma ERECTUS produced an appreciable quantity of essential oil, i.e., 1.8% fw, which was similar in its constituents to that obtained from 1-year-old plants, whether naturally grown or IN VITRO-raised potted plants. However, the quantity of various constituents identified so far was generally, but marginally, less in the former case than the latter two kinds of 1-year-old plants with the exception of bornyl acetate and 1,8-cineole, the concentrations of which were higher in the proliferated shoots than the plants. The essential oil content of 1-year-old naturally grown plants was 2.4% fw, while it was 2.38% fw in the IN VITRO-raised potted plants of the same age.

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