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1.
Chinese Medical Journal ; (24): 2083-2087, 2008.
Artículo en Inglés | WPRIM | ID: wpr-350747

RESUMEN

<p><b>BACKGROUND</b>Sericin peptide (SP) has shown a powerful anti-oxidant property in a host of studies. The present study was designed to investigate the possible protective effects of SP against alcohol-induced gastric lesions in mice and to explore the potential mechanisms.</p><p><b>METHODS</b>Animals were randomly divided into 5 groups: control, alcohol (56%, 14.2 ml/kg), SP-treated mice (0.2, 0.4, 0.8 g/kg). Mice were pretreated with SP before administering alcohol, the concentration of ethanol in serum and urine, the contents of malondialdehyde (MDA), glutathione (GSH) and the glutathione peroxidase (GSH-PX), catalase (CAT) and superoxide dismutase (SOD) activities in the gastric mucosa were measured, subsequently, the pathological evaluation of stomach was also observed.</p><p><b>RESULTS</b>Of the animals pre-treated with SP (0.4, 0.8 g/kg), the concentration of ethanol in serum was significantly decreased, while increased in urine as compared to the alcohol-administered alone animals. Alcohol administration caused severe gastric damage as indicated by markedly increased MDA levels and decreased antioxidants, such as reduced GSH, GSH-PX and SOD in the gastric tissue while the CAT activity was not altered. On SP administration there was a reversal in these values towards normal. Histopathological studies confirmed the beneficial role of SP, which was in accordance with the biochemical parameters.</p><p><b>CONCLUSIONS</b>SP could protect gastric mucosa from alcohol-induced mucosal injury. These gastroprotective effects might be due to increasing 'first-pass metabolism' in the stomach and hastening ethanol elimination directly through the urine. SP might also play an important role in the protection of the structure and function of gastric mitochondria, at least partly based on their anti-oxidant effect.</p>


Asunto(s)
Animales , Masculino , Ratones , Aminoácidos , Citoprotección , Etanol , Sangre , Toxicidad , Orina , Mucosa Gástrica , Patología , Glutatión , Metabolismo , Ratones Endogámicos ICR , Sericinas , Farmacología , Superóxido Dismutasa , Metabolismo
2.
China Journal of Chinese Materia Medica ; (24): 2282-2285, 2007.
Artículo en Chino | WPRIM | ID: wpr-324359

RESUMEN

<p><b>OBJECTIVE</b>To study the protective effects of Panax japonics (PJ) on alcohol-induced gastric lesion in mice and the possible mechanisms.</p><p><b>METHOD</b>Male ICR mice were randomized into six groups: normal, control, PJ (1.5, 3.0, 6.0 g x kg(-1)) and Yinduoan (1.5 g x kg(-1)). The mice were pretreated with PJ before administering ethanol to observe the effect on the concentration of ethanol in serum and urine. The contents of MDA, GSH and GSH-PX, CAT and SOD activities were measured in serum and gastric mucosa, and subsequently, the pathological evaluation of stomach was also observed.</p><p><b>RESULT</b>The concentration of ethanol in serum was evidently decreased after PJ (1.5, 3.0 g x kg(-1)) was administrated because the ethanol was eliminated fleetly through urine. Synchronously the PJ reduced the content of MDA and increased the GSH increased in serum and gastric, besides, it increased the enzymatic activities of GSHPX, CAT and SOD, and the ethanol-induced gastric mitochondria structure injury were ameliorated so as to make the function to normal.</p><p><b>CONCLUSION</b>Based on these observations, one could conclude that the PJ is a potent protective agent against ethanol-induced gastric damages. One mechanism may be related with inhibiting the absorbability of ethanol at gastrointestinal tract, decreasing the concentration of ethanol in serum, and accelerating the ethanol elimination through urine so as to alleviate the ethanol-induced damage to gastrointestinal mucosal, enhancing the first-pass metabolism in stomach, and particularly increasing the antioxidant levels in serum and gastric. These gastroprotective effects might be, at least partly, through ameliorating the gastric mitochondria structure.</p>


Asunto(s)
Animales , Masculino , Ratones , Catalasa , Sangre , Metabolismo , Medicamentos Herbarios Chinos , Farmacología , Usos Terapéuticos , Etanol , Mucosa Gástrica , Metabolismo , Patología , Glutatión , Sangre , Metabolismo , Glutatión Peroxidasa , Sangre , Metabolismo , Malondialdehído , Sangre , Metabolismo , Ratones Endogámicos ICR , Microscopía Electrónica , Mitocondrias , Panax , Química , Fitoterapia , Plantas Medicinales , Química , Sustancias Protectoras , Farmacología , Usos Terapéuticos , Distribución Aleatoria , Gastropatías , Sangre
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