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1.
Am J Chin Med ; 50(4): 1133-1153, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35543160

RESUMEN

Salidroside, an active ingredient in Rhodiola rosea, has potent protective activity against cerebral ischemia. However, the mechanisms underlying its pharmacological actions are poorly understood. In this study, we employed a mouse middle cerebral artery occlusion (MCAO) and cellular oxygen and glucose deprivation (OGD) models to test the hypothesis that salidroside may restore mitochondrial quality control in neurons by modulating the relevant signaling. The results indicated that salidroside mitigated almost 40% the ischemia-induced brain infarct volumes in mice and the OGD-decreased viability of neurons to ameliorate the mitochondrial functions. Furthermore, salidroside treatment alleviated the OGD- or ischemia-induced imbalance of mitochondrial fission and fusion, mitophagy and promoted mitochondrial biogenesis in neurons by attenuating the AMPK activity. Moreover, salidroside alleviated 50% the OGD-promoted mitochondrial calcium fluorescence intensity and 5% mitochondria-associated membrane (MAM) area by down-regulating GRP75 expression independent of the AMPK signaling. Finally, similar findings were achieved in primary mouse neurons. Collectively, these data indicate that salidroside effectively restores the mitochondria dynamics, facilitates mitochondrial biogenesis by attenuating the AMPK signaling, and maintains calcium homeostasis in neurons independent of the AMPK activity.


Asunto(s)
Proteínas Quinasas Activadas por AMP , Isquemia Encefálica , Proteínas Quinasas Activadas por AMP/metabolismo , Animales , Isquemia Encefálica/tratamiento farmacológico , Isquemia Encefálica/metabolismo , Calcio/metabolismo , Glucosa/metabolismo , Glucósidos , Isquemia/metabolismo , Ratones , Mitocondrias/metabolismo , Neuronas , Fenoles
2.
Mol Immunol ; 57(2): 263-73, 2014 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-24211534

RESUMEN

Recently, considerable interest has been focused on immunostimulants to reduce diseases in crab aquaculture. However, information regarding to the related immune-enhancing proteins in crabs is not available yet. In this study, rhubarb polysaccharides were tested for enhancement of the immune activity in crab Scylla paramamosain. Compared with those in the control group, values of, phenoloxidase (PO), alkaline phosphatase (AKP) and alkaline phosphatasein (ACP) activity in the, experimental group were improved significantly 4 d after the treatment. Furthermore, 15 and 17 altered proteins from haemocytes and hepatopancreas, respectively, were found in rhubarb polysaccharide-treated crabs using 2-DE approach. Of these, hemocyanin, chymotrypsin, cryptocyanin, C-type lectin receptor, and ferritin protein were identified by mass spectrometry. In addition, RT-PCR, analysis showed that the mRNA levels of hemocyanin and chymotrypsin increased about 2.4- and 1.4-fold in the experiment group. Moreover, the hemocyanin gene in S. paramamosain (SpHMC) was, cloned and characterized. SpHMC contains one open reading frame of 2022 bp and encodes a polypeptide of 673 amino acids. It is clustered into one branch along with crab hemocyanin in a phylogenetic tree. The mRNA transcripts of SpHMC were detected mainly in the tissues of, hepatopancreas, hemocyte and intestines, and its levels were up-regulated significantly in hemocytes, of S. paramamosain treated with Vibrio parahemolyticus, Beta streptococcus or poly I:C for 6-48 h. Taken together, these studies found 5 related immune-enhancing proteins and a novel heomcyanin homologue with potential pathogen-resistant activities in crab.


Asunto(s)
Adyuvantes Inmunológicos/metabolismo , Braquiuros/metabolismo , Polisacáridos/metabolismo , Rheum/metabolismo , Fosfatasa Alcalina/metabolismo , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Quimotripsina/genética , Quimotripsina/metabolismo , Clonación Molecular , Perfilación de la Expresión Génica , Hemocianinas/genética , Hemocianinas/metabolismo , Hemocitos/metabolismo , Hepatopáncreas/metabolismo , Lectinas Tipo C/metabolismo , Espectrometría de Masas , Datos de Secuencia Molecular , Monofenol Monooxigenasa/metabolismo , Preparaciones de Plantas/metabolismo , Poli I-C/inmunología , ARN Mensajero/biosíntesis , Análisis de Secuencia de ADN , Streptococcus/inmunología , Vibrio/inmunología
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