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1.
Biochem Biophys Res Commun ; 506(4): 773-779, 2018 12 02.
Artículo en Inglés | MEDLINE | ID: mdl-30389140

RESUMEN

Cachexia, observed in most cancer patients, is a syndrome that includes wasting of bodily energy reserves and is characterized by muscle atrophy and fat loss. We have previously demonstrated that isoflavones, such as genistein and daidzein, prevent muscle wasting in tumor-bearing mice. In this study, we examined the effect of morin, a flavonoid, on cachexia. The wet weight and myofiber size of muscles in Lewis lung carcinoma (LLC) cell-bearing mice fed a normal diet were decreased, compared with those in control mice fed a normal diet. In contrast, intake of morin prevented the reduction of muscle wet weight and myofiber size. Moreover, the tumor weight in mice fed the morin diet was lower than that in mice fed the normal diet. Both cell viability and protein synthetic ability of LLC cells were reduced by treatment with morin, but C2C12 myotubes were not affected. Binding assay using morin-conjugated magnetic beads identified ribosomal protein S10 (RPS10) as a target protein of morin. Consistent with the result of morin treatment, knockdown of RPS10 suppressed LLC cell viability. These results suggest that morin indirectly prevents muscle wasting induced by cancer cachexia by suppressing cancer growth via binding to RPS10.


Asunto(s)
Caquexia/tratamiento farmacológico , Caquexia/metabolismo , Carcinoma Pulmonar de Lewis/metabolismo , Carcinoma Pulmonar de Lewis/patología , Flavonoides/uso terapéutico , Músculo Esquelético/patología , Proteínas Ribosómicas/metabolismo , Animales , Peso Corporal , Caquexia/patología , Línea Celular Tumoral , Proliferación Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Dieta , Flavonoides/farmacología , Masculino , Ratones Endogámicos C57BL , Fibras Musculares Esqueléticas/patología , Músculo Esquelético/efectos de los fármacos , Tamaño de los Órganos , Unión Proteica/efectos de los fármacos , Biosíntesis de Proteínas/efectos de los fármacos
2.
Br J Nutr ; 113(9): 1489-98, 2015 May 14.
Artículo en Inglés | MEDLINE | ID: mdl-25851425

RESUMEN

Partially hydrolysed guar gum (PHGG), a soluble dietary fibre, has been shown to provide many health benefits. Previous studies had suggested that the combination of PHGG with protein provided a significant satiation effect on visual analogue scales (VAS). What was lacking was only the effect of administration of small doses of PHGG on post-meal satiation and subsequent energy intake. The objectives of the present investigations were to find the subjective perception of post-meal satiety with acute and long term administration of small amounts of PHGG alone with food, its effects on subsequent energy intake and the comparative effects among different types of soluble fibres. The following three separate studies were conducted: in study 1, healthy subjects (n 12) consumed PHGG along with breakfast, lunch and an evening snack; in study 2, healthy subjects (n 24) consumed 2 g of PHGG or dextrin along with yogurt as breakfast for 2 weeks; in study 3, healthy subjects (n 6) took 6 g each of either PHGG or indigestible dextrin or inulin along with lunch. In all the studies, various satiety parameters were measured on VAS before and after consumption of PHGG. The addition of PHGG showed significant (P < 0.05) acute (studies 1 and 3) and long-term (studies 1 and 2) satiety effects compared to the control and/or an equal amount of carbohydrate or other types of soluble fibre. Study 2 also indicated that the prolonged consumption of PHGG may significantly (P < 0.05) reduce energy intake from whole-day snacking. PHGG could be an ideal natural soluble fibre for delivering acute and long term satiety effects for comfortable appetite control.


Asunto(s)
Fibras de la Dieta/administración & dosificación , Ingestión de Energía/efectos de los fármacos , Galactanos/administración & dosificación , Mananos/administración & dosificación , Percepción , Gomas de Plantas/administración & dosificación , Saciedad/efectos de los fármacos , Adulto , Regulación del Apetito , Desayuno , Dextrinas/administración & dosificación , Carbohidratos de la Dieta/administración & dosificación , Femenino , Galactanos/química , Humanos , Hambre , Hidrólisis , Inulina/administración & dosificación , Almuerzo , Masculino , Mananos/química , Gomas de Plantas/química , Periodo Posprandial , Bocadillos , Solubilidad , Yogur
3.
Rapid Commun Mass Spectrom ; 23(13): 2053-60, 2009 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19504477

RESUMEN

The primary structure of the deteriorated recombinant human basic fibroblast growth factor (rhbFGF) was determined by ultra-performance liquid chromatography and electrospray ionization quadrupole time-of-flight mass spectrometry (UPLC/ESI-QTOF-MS) with in-source collision-induced dissociation (CID). The rhbFGFs before and after treatment with hydrogen peroxide (H(2)O(2)) were separated using an ACQUITY UPLC BEH300 C18 column (1.7 microm, 150 mm x 2.1 mm i.d.) with a gradient elution of a mixture of water/acetonitrile containing 0.1% formic acid. The separated proteins were then detected by a SYNAPT High Definition Mass Spectrometry system (SYNAPT-MS). Two methionine (Met) residues in the rhbFGF structure were oxidized to Met-sulfoxide (Met-O) in 0.03% H(2)O(2) at pH 2.0. As the result, three peaks, except for the peak of rhbFGF, appeared on the chromatogram. The three proteins corresponding to each peak were estimated as the denatured rhbFGFs including the Met-O residue(s) with TOF-MS. Furthermore, the position of the Met-O residue(s) was efficiently identified by UPLC/ESI-QTOF-MS using the in-source CID technique. The proposed method seems to be very useful for the structural elucidation of proteins, because the oxidized Met residues in rhbFGF were easily and rapidly identified.


Asunto(s)
Cromatografía Líquida de Alta Presión/métodos , Factor 2 de Crecimiento de Fibroblastos/química , Metionina/química , Espectrometría de Masa por Ionización de Electrospray/métodos , Secuencia de Aminoácidos , Humanos , Cinética , Datos de Secuencia Molecular , Oxidación-Reducción , Proteínas Recombinantes/química , Espectrometría de Masa por Ionización de Electrospray/instrumentación
4.
Pharmacol Biochem Behav ; 111: 128-35, 2013 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-24051231

RESUMEN

PURPOSE: Theanine, an amino acid in tea, has significant anti-stress effect on experimental animals under psychosocial stress. Anti-stress effect of theanine on humans was evaluated in 5th-year university students during pharmacy practice. METHOD: The study design was a single-blind group comparison and participants (n=20) were randomly assigned to theanine or placebo groups. Theanine or placebo (lactose) tablets (200 mg, twice a day, after breakfast and lunch) were taken from 1 week prior to the pharmacy practice and continued for 10 days in the practice period. To assess the anxiety of the participants, the state-trait anxiety inventory test was carried out before the pharmacy practice. Salivary α-amylase activity (sAA) was measured as a marker of sympathetic nervous system activity. RESULTS: In the placebo-group, sAA in the morning (pre-practice sAA) was higher than in theanine-group during the pharmacy practice (p=0.032). Subjective stress was significantly lower in the theanine-group than in the placebo-group (p=0.020). These results suggest that theanine intake had anti-stress effect on students. Furthermore, students with higher pre-practice sAA showed significantly higher trait anxiety in both groups (p=0.015). Similarly, higher pre-practice sAA was correlated to shorter sleeping time in both groups (p=0.41×10(-3)). CONCLUSION: Stressful condition increased the level of sAA that was essentially affected by individual trait anxiety. The low levels of pre-practice sAA and subjective stress in the theanine-group suggest that theanine intake suppressed initial stress response of students assigned for a long-term commitment of pharmacy practice.


Asunto(s)
Educación en Farmacia , Glutamatos/uso terapéutico , Saliva/enzimología , Estrés Psicológico/tratamiento farmacológico , Estudiantes/psicología , alfa-Amilasas/metabolismo , Adulto , Femenino , Humanos , Masculino , Placebos , Método Simple Ciego , Recursos Humanos , Adulto Joven
5.
Planta Med ; 70(4): 299-304, 2004 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-15095143

RESUMEN

While searching for new estrogenic compounds from the plant kingdom, we investigated an extract of the seeds of Cuscuta chinensis (Convolvulaceae) which showed potency for stimulating MCF-7 cell proliferation. A novel resin glycoside, cuscutic resinoside A ( 6) was isolated along with five known compounds from the extract. The structure was deduced from its spectral data as (11 S)-hydroxyhexadecanoic acid 11- O-alpha- L-(4- O-2 R,3 R-nilylrhamnopyranosyl)-(1-->2)- O-alpha- L-rhamnopyranosyl-(1,2-lactone) forming a unique 15-membered macrocyclic lactone. The compound significantly stimulated not only MCF-7 cell proliferation but also T47D human breast cancer cells at a concentration of 10 microM. Along with cuscutamine ( 1) and kaempferol ( 4), 6 was tested in the transient luciferase reporter assay and was found to have different luciferase inducing activity characteristics from the other compounds. These results suggest that 6 stimulated cancer cell proliferation by a different mechanism from 1 and 4.


Asunto(s)
División Celular/efectos de los fármacos , Cuscuta , Glucolípidos/farmacología , Isoflavonas/farmacología , Fitoterapia , Extractos Vegetales/farmacología , Preparaciones de Plantas/farmacología , Neoplasias de la Mama/patología , Línea Celular Tumoral/efectos de los fármacos , Femenino , Humanos , Fitoestrógenos , Extractos Vegetales/química , Semillas
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