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1.
J Agric Food Chem ; 53(11): 4593-8, 2005 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-15913331

RESUMEN

Fifty-four polyphenols isolated from tea leaves were evaluated for their inhibitory activities against pancreatic lipase, the key enzyme of lipid absorption in the gut. (-)-Epigallocatechin 3-O-gallate (EGCG), which is one of major polyphenols in green tea, showed lipase inhibition with an IC50 of 0.349 microM. Moreover, flavan-3-ol digallate esters, such as (-)-epigallocatechin-3,5-digallate, showed higher activities of inhibition on lipase with an IC50 of 0.098 microM. On the other hand, nonesterified flavan-3-ols, such as (+)-catechin, (-)-epicatechin, (+)-gallocatechin, and (-)-epigallocatechin, showed zero and/or the lowest activities against pancreatic lipase (IC50 > 20 microM). These data suggested that the presence of galloyl moieties within the structure was required for enhancement of pancreatic lipase inhibition. It is well-known that flavan-3-ols are polymerized by polyphenol oxidase and/or heating in a manufacturing process of oolong tea. Oolonghomobisflavans A and B and oolongtheanin 3'-O-gallate, which are typical in oolong tea leaves, showed strong inhibitory activities with IC50 values of 0.048, 0.108, and 0.068 microM, respectively, even higher than that of EGCG. The oolong tea polymerized polyphenols (OTPP) were prepared for the assay from oolong tea extract, from which the preparation effectively subtracted the zero and/or less-active monomeric flavan-3-ols by preparative high-performance liquid chromatography. The weight-average molecular weight (Mw) and number-average molecular-weight (Mn) values of OTPP were 2017 and 903, respectively, by using gel permeation choromatography. OTPP showed a 5-fold stronger inhibition against pancreatic lipase (IC50 = 0.28 microg/mL) by comparison with that of the tannase-treated OTPP (IC50 = 1.38 microg/mL). These data suggested that the presence of galloyl moieties within their chemical structures and/or the polymerization of flavan-3-ols were required for enhancement of pancreatic lipase inhibition.


Asunto(s)
Camellia sinensis/química , Inhibidores Enzimáticos/farmacología , Flavonoides/farmacología , Lipasa/antagonistas & inhibidores , Páncreas/enzimología , Fenoles/farmacología , Hojas de la Planta/química , Cromatografía en Gel , Flavonoides/química , Flavonoides/aislamiento & purificación , Flavonoles/química , Flavonoles/farmacología , Fenoles/química , Fenoles/aislamiento & purificación , Polímeros/química , Polímeros/farmacología , Polifenoles , Relación Estructura-Actividad
2.
Life Sci ; 70(21): 2509-20, 2002 Apr 21.
Artículo en Inglés | MEDLINE | ID: mdl-12173414

RESUMEN

We investigated the effects of astaxanthin on the antitumor effector activity of natural killer (NK) cells suppressed by stress in mice in order to define the immunological significance of astaxanthin (ASX) when combined with restraint stress treatment. When the mice were treated with restraint stress alone, the total number of spleen cells, and the level NK cell activity per spleen were reduced to a nadir on day 3. The stress also caused a significant increase in the lipid peroxidation of liver tissue. ASX (100 mg/kg/day, p.o., 4 days) improved the immunological dysfunction induced by restraint stress. On the other hand, metastatic nodules were observed in the livers of syngenic DBA/2 mice on day 12 after inoculation of P815 mastocytoma cells. Hepatic metastasis was promoted further by restraint stress when applied on day 3 before the inoculation of P815. Daily oral administration of ASX (1 mg/kg/day, p.o., 14 days) markedly attenuated the promotion of hepatic metastasis induced by restraint stress. These results suggested that astaxanthin improves antitumor immune responses by inhibiting of lipid peroxidation induced by stress.


Asunto(s)
Antineoplásicos Fitogénicos/farmacología , Antineoplásicos Fitogénicos/uso terapéutico , Antioxidantes/farmacología , Antioxidantes/uso terapéutico , Metástasis de la Neoplasia/prevención & control , Estrés Psicológico/patología , beta Caroteno/análogos & derivados , beta Caroteno/farmacología , beta Caroteno/uso terapéutico , Animales , Antineoplásicos Fitogénicos/farmacocinética , Antioxidantes/farmacocinética , Células Cultivadas , Femenino , Inmunosupresores/farmacología , Células Asesinas Naturales/efectos de los fármacos , Peroxidación de Lípido/efectos de los fármacos , Hígado/efectos de los fármacos , Hígado/metabolismo , Neoplasias Hepáticas/prevención & control , Neoplasias Hepáticas/secundario , Sarcoma de Mastocitos/patología , Sarcoma de Mastocitos/prevención & control , Ratones , Ratones Endogámicos C57BL , Ratones Endogámicos DBA , Trasplante de Neoplasias/patología , Restricción Física , Sustancias Reactivas al Ácido Tiobarbitúrico/metabolismo , Distribución Tisular , Células Tumorales Cultivadas , Xantófilas , beta Caroteno/farmacocinética
3.
Biosci Biotechnol Biochem ; 71(4): 971-6, 2007 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-17420597

RESUMEN

Oolong tea-polymerized polyphenols (OTPP) are characterized polyphenols produced from semi-fermented tea (oolong tea). In the present study, we evaluated the suppressive effects of oolong tea extract and OTPP on postprandial hypertriglyceridemia in rats and mice. Lymphatic recovery of triglycerides in rats cannulated in the thoracic duct was delayed by the administration of oolong tea extract at 100 and 200 mg per head, and more effectively than with green tea extract. OTPP delayed lymphatic triglyceride absorption at 20 mg/head, though (-)-epigallocatechin gallate (EGCG) did not do so at the same dose. OTPP also suppressed postprandial hypertriglyceridemia after administration of olive oil in mice. The area under the curve (AUC) of plasma triglycerides was significantly decreased, by 53% and 76%, in the 500 and 1,000 mg/kg OTPP groups respectively, as compared with the control group. These results suggest that OTPP is responsible for the suppression of hypertriglyceridemia by ingestion of oolong tea.


Asunto(s)
Flavonoides/farmacología , Hipertrigliceridemia/tratamiento farmacológico , Fenoles/farmacología , Periodo Posprandial/fisiología , Té/química , Animales , Catequina/análogos & derivados , Catequina/farmacología , Sistema Linfático/efectos de los fármacos , Sistema Linfático/metabolismo , Masculino , Ratones , Ratones Endogámicos C57BL , Polifenoles , Ratas , Ratas Sprague-Dawley , Triglicéridos/metabolismo
4.
Biosci Biotechnol Biochem ; 70(5): 1118-26, 2006 May.
Artículo en Inglés | MEDLINE | ID: mdl-16717411

RESUMEN

Sesame peptide powder (SPP) exhibited angiotensin I-converting enzyme (ACE) inhibitory activity, and significantly and temporarily decreased the systolic blood pressure (SBP) in spontaneously hypertensive rats (SHRs) by a single administration (1 and 10 mg/kg). Six peptide ACE inhibitors were isolated and identified from SPP. The representative peptides, Leu-Val-Tyr, Leu-Gln-Pro and Leu-Lys-Tyr, could competitively inhibit ACE activity at respective Ki values of 0.92 microM, 0.50 microM, and 0.48 microM. A reconstituted sesame peptide mixture of Leu-Ser-Ala, Leu-Gln-Pro, Leu-Lys-Tyr, Ile-Val-Tyr, Val-Ile-Tyr, Leu-Val-Tyr, and Met-Leu-Pro-Ala-Tyr according to their content ratio in SPP showed a strong antihypertensive effect on SHR at doses of 3.63 and 36.3 microg/kg, which accounted for more than 70% of the corresponding dosage for the SPP-induced hypotensive effect. Repeated oral administration of SPP also lowered both SBP and the aortic ACE activity in SHR. These results demonstrate that SPP would be a beneficial ingredient for preventing and providing therapy against hypertension and its related diseases.


Asunto(s)
Inhibidores de la Enzima Convertidora de Angiotensina/farmacología , Antihipertensivos/farmacología , Hipertensión/enzimología , Oligopéptidos/farmacología , Peptidil-Dipeptidasa A/efectos de los fármacos , Sesamum/química , Administración Oral , Secuencia de Aminoácidos , Inhibidores de la Enzima Convertidora de Angiotensina/química , Inhibidores de la Enzima Convertidora de Angiotensina/aislamiento & purificación , Animales , Antihipertensivos/química , Antihipertensivos/aislamiento & purificación , Presión Sanguínea/efectos de los fármacos , Hidrólisis , Oligopéptidos/química , Oligopéptidos/aislamiento & purificación , Preparaciones de Plantas/administración & dosificación , Preparaciones de Plantas/química , Proteínas de Plantas/química , Proteínas de Plantas/aislamiento & purificación , Ratas , Ratas Endogámicas SHR
5.
Biol Pharm Bull ; 26(3): 383-5, 2003 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-12612454

RESUMEN

We investigated the inhibitory effect of Cyclocarya paliurus (Batal.) Iljinskaja (C. paliurus) extract on postprandial hyperlipemia in mice. A single oral administration of C. paliurus extract (250 mg/kg) suppressed an increase in plasma triacylgycerol (TG) levels when fed with 5 ml/kg of lard and olive oil. The inhibition rates were 28.6% and 24.1%, respectively, but free fatty acid (FFA) levels in plasma were not significantly affected as compared with control group mice. In addition, C. paliurus extract showed inhibitory activity toward pancreatic lipase, a key enzyme of dietary TG absorption, with an IC(50) of 9.1 microg/ml in vitro. Our results suggested that the hypolipemic action of C. paliurus extract was probably interrelated with suppression of the activity of digestive lipase, and as a result, the blood lipid level was reduced.


Asunto(s)
Ácidos Grasos no Esterificados/sangre , Hipolipemiantes/farmacología , Juglandaceae/química , Triglicéridos/sangre , Animales , Relación Dosis-Respuesta a Droga , Medicamentos Herbarios Chinos/farmacología , Lipasa/antagonistas & inhibidores , Masculino , Ratones , Ratones Endogámicos ICR , Plantas Medicinales , Factores de Tiempo
6.
Biosci Biotechnol Biochem ; 67(4): 877-80, 2003 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-12784631

RESUMEN

This study examined the hypoglycaemic activity of Cyclocarya paliurus (Batal.) Iljinskaja (C. paliurus) in ICR mice by oral glucose tolerance testing. The blood glucose level was significantly lower in the C. paliurus extract treatment group than in the control group after animals were given sucrose. This difference was not observed following the administration of glucose. We demonstrated that the chronological change in the level of blood glucose in genetically hyperglycemic obese KK-Ay mice is significantly lower when C. paliurus extract is administered daily for three weeks. An in vitro study showed that C. paliurus inhibits alpha-glucosidase, a disaccharide-degrading enzyme in the small intestinal mucosa, leading to a decrease in the absorption of glucose into the blood and a subsequent lowering of the blood glucose level.


Asunto(s)
Glucemia/efectos de los fármacos , Diabetes Mellitus/tratamiento farmacológico , Medicamentos Herbarios Chinos/farmacología , Hipoglucemiantes/farmacología , Animales , Relación Dosis-Respuesta a Droga , Inhibidores Enzimáticos/farmacología , Prueba de Tolerancia a la Glucosa , Inhibidores de Glicósido Hidrolasas , Mucosa Intestinal/enzimología , Masculino , Ratones , Ratones Endogámicos ICR , Ratones Obesos , Plantas Medicinales
7.
Biol Pharm Bull ; 27(7): 1093-8, 2004 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-15256746

RESUMEN

In the present study, we investigated the antioxidative effect of oolong tea in vitro and in vivo using the oxygen radical absorbance capacity (ORAC) assay. An oolong tea extract, catechin and related compounds suppressed the oxidation of fluorescence induced by AAPH in a dose-dependent manner, that is, they prolonged the antioxidant time in vitro. Oral administration of the oolong tea extract to mice treated with restraint stress increased ORAC activity in plasma as compared with a stress control group. The extract also increased plasma vitamin C levels, and there was a good relationship between ORAC activity and the vitamin C level in plasma. The elevation of plasma ORAC and vitamin C level may have been related to the stress-relieving effect of oolong tea. These effects are probably due to the antioxidative properties of the tea. Thus, these findings suggested that oolong tea has beneficial effects on health related to its antioxidative action.


Asunto(s)
Antioxidantes/metabolismo , Especies Reactivas de Oxígeno/sangre , Estrés Fisiológico/sangre , , Animales , Ácido Ascórbico/sangre , Relación Dosis-Respuesta a Droga , Masculino , Ratones , Ratones Endogámicos ICR , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/farmacología , Restricción Física
8.
Biol Pharm Bull ; 26(10): 1393-7, 2003 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-14519942

RESUMEN

In normal mice, plasma histamine levels were 29.4+/-10.1 pmol/ml. When 0.1 microg of lipopolysaccharide (LPS) was intravenously injected into Propionibacterium acnes (P. acnes)-primed ICR mice, histamine levels increased remarkably to 61.2+/-15.9 pmol/ml (p<0.001). An increase was also observed in liver tissues. Oral administration of histidine at 200 mg/kg once daily for 5 d before intravenous LPS injection increased the plasma alanine aminotransferase (ALT) activity to 2936.5+/-356.3 IU/l, a significant change compared with the controls (2244.8+/-425.5 IU/l, p<0.05). The 24 h survival rate after LPS injection was 72.7% in the mice treated with 50 mg/kg of ranitidine, in contrast with 50% in the control group although the treatment did not significantly decrease the plasma ALT activity. On the other hand, 50 mg/kg of pyrilamine significantly reduced plasma ALT activity (p<0.001). The results suggested that histamine levels are related to hepatic damage in the P. acnes plus LPS induction of liver injury.


Asunto(s)
Modelos Animales de Enfermedad , Histamina/sangre , Lipopolisacáridos/toxicidad , Hepatopatías/sangre , Propionibacterium acnes , Alanina Transaminasa/sangre , Animales , Enfermedad Hepática Inducida por Sustancias y Drogas , Sinergismo Farmacológico , Hepatopatías/microbiología , Masculino , Ratones , Ratones Endogámicos ICR
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