La enfermedad de Alzheimer (EA) se caracteriza por una acumulación severa de placas amiloides y ovillos neurofibrilares acompañados de disfunciones cognitivas severas que conducen a cambios importantes que afectan la calidad del patrón de vida diaria del paciente. El objetivo del presente estudio es investigar los efectos de la administración de células madre mesenquimales (MSC) y/o granos de kéfir de leche en el modelo de tipo neuroinflamatorio de EA inducida por LPS de manera alternativa. Se observó que una elevación significativa del perfil lipídico y el estrés oxidativo estaban relacionados con EA de tipo neuroinflamatoria inducida con LPS. La expresión del gen BDNF, Bcl-2 y seladin-1 también se redujo significativamente en ratas con EA, mientras que la expresión relativa de Bax aumentó significativamente. La administración de granos de kéfir de leche y/o MSC suprimió los inconvenientes de la EA incluyendo cambios de comportamiento y memoria. Conclusión: La administración previa y la coadministración de granos de kéfir de leche con MSC pueden actuar como un neuromodulador activo que atenúa el proceso inflamatorio patológico subyacente que acompaña a la EA, lo que resulta en la progresión de daños en el tejido cerebral.
It is known that xanthine oxidoreductase contributes significantly to ischemia/reperfusion injury by generating reactive oxygen species. Ischemia-modified albumin (IMA) is a biomarker of acute myocardial ischemia with high sensitivity but moderate specificity. Our study aims to evaluate the xanthine oxidase (XO) system and the IMA level in the serum of patients with ischemic heart disease, and their correlation with traditional cardiac markers. The study was conducted on 60 patients with ischemic heart disease and 22 healthy subjects (control group). Subjects were divided into three groups: group I (30 patients with ST-elevated myocardial infarction), group II (30 patients with chronic stable angina), and the control group (22 subjects). The patients and controls had laboratory tests performed including lipid profile, cardiac enzymes, XO, uric acid, and IMA. The serum levels of XO and IMA were significantly higher in group I (1.65 ± 0.29 U/ml and 0.58 ± 0.15 ABSU, respectively) than in group II (1.11 ± 0.20 U/ml and 0.29 ± 0.10 ABSU, respectively) and the control group (0.95 ± 0.16 U/ml and 0.24 ± 0.08 ABSU, respectively) (P < 0.001). There was a significant positive correlation between XO and IMA in group I. Also, there was significant positive correlation between XO or IMA and other cardiac markers, with the highest level of significance between IMA and creatine kinase (CK-MB). In group II only XO activity was significantly elevated in comparison with controls. These results confirm the role of XO enzyme in ischemic heart disease with involvement of IMA, at a detectable level, during the early necrotic phase.
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