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Salles, G. N.

Publications and source records attributed to Salles, G. N..

2 recordsLinked to original sources

EVALUATION OF TAURINE'S NEUROPROTECTIVE EFFECTS ON SH-SY5Y CELLS UNDER OXIDATIVE STRESS

Alzheimers disease (AD) is a type of dementia that affects millions of people. Although there is no cure, several study strategies seek to elucidate the mechanisms of the disease. Recent studies address the benefits of taurine. Thus, the present study aims to analyze the neuroprotective effect of taurine on human neuroblastoma, using an in vitro experimental model of oxidative stress induced by hydrocortisone in the SH-SY5Y cell line as a characteristic model of AD. The violet crystal assay was used for cell viability and the evaluation of cell morphology was performed by scanning electron microscopy (SEM). After pretreatment with taurine, the SH-SY5Y cell showed an improvement in cell viability in the face of oxidative stress and improved cell morphology. Thus, the treatment presented a neuroprotective effect. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=113 SRC="FIGDIR/small/441504v1_ufig1.gif" ALT="Figure 1"> View larger version (23K): org.highwire.dtl.DTLVardef@12dcb58org.highwire.dtl.DTLVardef@1810110org.highwire.dtl.DTLVardef@6cc235org.highwire.dtl.DTLVardef@424491_HPS_FORMAT_FIGEXP M_FIG C_FIG

cell biology↗

Leptin reduces pathology and increases adult neurogenesis in a transgenic mouse model of Alzheimer’s disease

Alzheimers disease (AD) is the most common dementia worldwide, and is characterized by the presence, in the brain tissue, of extracellular senile plaques formed by amyloid beta (A{beta}) peptide and intracellular neurofibrillary tangles of hyperphosphorylated Tau protein. These changes lead to progressive neuronal degeneration and dysfunction, resulting in severe brain atrophy and cognitive deficits. With the discovery that neurogenesis persists in the adult mammalian brain, including brain regions affected by AD, studies of the use of neural stem cells for treatment of neurodegenerative diseases in order to repair and/or prevent neuronal cell loss have increased. Here we show that leptin increases neurogenesis in the dentate gyrus of adult mice as well as in the subventricular zone both in wild type and AD transgenic mouse model. Chronic administration of leptin to young mice increased neural stem cell proliferation with significant effects on differentiation and survival of newborn cells. Expression of the long form of leptin receptor, LepRb, was detected in the neurogenic niches by reverse transcription-PCR and immunohistochemistry. Moreover, leptin modulated astrogliosis and the formation of senile plaques. Additionally, leptin led to attenuation of A{beta}-induced neurodegeneration and superoxide anion production as revealed by Fluoro-Jade B and dihydroethidium (DHE) staining. Our study contributes to the understanding of the effects of leptin in the brain that may lead to the development of new therapies to treat Alzheimers disease.

neuroscience↗