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1.
J Mol Cell Cardiol ; 114: 211-219, 2018 01.
Artículo en Inglés | MEDLINE | ID: mdl-29158034

RESUMEN

AIMS: Calcific aortic valve disease is the most common heart valve disease in the Western world. Bicuspid and tricuspid aortic valve calcifications are traditionally considered together although the dynamics of the disease progression is different between the two groups of patients. Notch signaling is critical for bicuspid valve development and NOTCH1 mutations are associated with bicuspid valve and calcification. We hypothesized that Notch-dependent mechanisms of valve mineralization might be different in the two groups. METHODS AND RESULTS: We used aortic valve interstitial cells and valve endothelial cells from patients with calcific aortic stenosis with bicuspid or tricuspid aortic valve. Expression of Notch-related genes in valve interstitial cells by qPCR was different between bicuspid and tricuspid groups. Discriminant analysis of gene expression pattern in the interstitial cells revealed that the cells from calcified bicuspid valves formed a separate group from calcified tricuspid and control cells. Interstitial cells from bicuspid calcified valves demonstrated significantly higher sensitivity to stimuli at early stages of induced proosteogenic differentiation and were significantly more sensitive to the activation of proosteogenic OPN, ALP and POSTIN expression by Notch activation. Notch-activated endothelial-to-mesenchymal transition and the corresponding expression of HEY1 and SLUG were also more prominent in bicuspid valve derived endothelial cells compared to the cells from calcified tricuspid and healthy valves. CONCLUSION: Early signaling events including Notch-dependent mechanisms that are responsible for the initiation of aortic valve calcification are different between the patients with bicuspid and tricuspid aortic valves.


Asunto(s)
Válvula Mitral/metabolismo , Receptores Notch/metabolismo , Transducción de Señal , Válvula Tricúspide/metabolismo , Válvula Aórtica/metabolismo , Válvula Aórtica/patología , Estenosis de la Válvula Aórtica/sangre , Estenosis de la Válvula Aórtica/metabolismo , Biomarcadores/metabolismo , Calcinosis/sangre , Calcinosis/metabolismo , Diferenciación Celular , Análisis Discriminante , Células Endoteliales/metabolismo , Fibrosis , Regulación de la Expresión Génica , Humanos , Ligandos , Mesodermo/metabolismo , Músculo Liso/metabolismo , Osteoblastos/metabolismo , Osteogénesis , Osteopontina/sangre
2.
Bull Exp Biol Med ; 164(3): 371-375, 2018 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-29308559

RESUMEN

Comparative in vitro study examined the osteogenic potential of interstitial cells of aortic valve obtained from the patients with aortic stenosis and from control recipients of orthotopic heart transplantation with intact aortic valve. The osteogenic inductors augmented mineralization of aortic valve interstitial cells (AVIC) in patients with aortic stenosis in comparison with the control level. Native AVIC culture of aortic stenosis patients demonstrated overexpression of osteopontin gene (OPN) and underexpression of osteoprotegerin gene (OPG) in comparison with control levels. In both groups, AVIC differentiation was associated with overexpression of RUNX2 and SPRY1 genes. In AVIC of aortic stenosis patients, expression of BMP2 gene was significantly greater than the control level. The study revealed an enhanced sensitivity of AVIC to osteogenic inductors in aortic stenosis patients, which indicates probable implication of OPN, OPG, and BMP2 genes in pathogenesis of aortic valve calcification.


Asunto(s)
Estenosis de la Válvula Aórtica/genética , Válvula Aórtica/patología , Calcinosis/genética , Osteoblastos/metabolismo , Osteogénesis/genética , Células del Estroma/metabolismo , Válvula Tricúspide/metabolismo , Anciano , Válvula Aórtica/metabolismo , Válvula Aórtica/cirugía , Estenosis de la Válvula Aórtica/metabolismo , Estenosis de la Válvula Aórtica/patología , Estenosis de la Válvula Aórtica/cirugía , Ácido Ascórbico/farmacología , Proteína Morfogenética Ósea 2/genética , Proteína Morfogenética Ósea 2/metabolismo , Calcinosis/metabolismo , Calcinosis/patología , Calcinosis/cirugía , Diferenciación Celular , Subunidad alfa 1 del Factor de Unión al Sitio Principal/genética , Subunidad alfa 1 del Factor de Unión al Sitio Principal/metabolismo , Dexametasona/farmacología , Femenino , Regulación de la Expresión Génica , Glicerofosfatos/farmacología , Trasplante de Corazón , Humanos , Masculino , Proteínas de la Membrana/genética , Proteínas de la Membrana/metabolismo , Persona de Mediana Edad , Osteoblastos/efectos de los fármacos , Osteoblastos/patología , Osteogénesis/efectos de los fármacos , Osteopontina/genética , Osteopontina/metabolismo , Osteoprotegerina/genética , Osteoprotegerina/metabolismo , Fosfoproteínas/genética , Fosfoproteínas/metabolismo , Cultivo Primario de Células , Células del Estroma/efectos de los fármacos , Células del Estroma/patología , Válvula Tricúspide/patología , Válvula Tricúspide/cirugía
3.
Anesteziol Reanimatol ; 61(6): 455-461, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-29894617

RESUMEN

Background The presence ofpulmonary arterial hypertension (PAH) in pregnant women increases mortality up to 12- 30% and up to 50% when PAH is associated with Eisenmenger syndrome. Due to low prevalence of PAH in pregnancy many aspects ofperioperative management are still unclear. THE AIM: To summarize our approaches to the anesthesia and intensive care in pregnant women with PAH. MATERIALS AND METHODS: 21 pregnant women with PAH (systolic pulmonary artery pressure (SPAP) higher than 60 mm Hg)-who underwent delivery by Caesarean section in 2010 - 2015 were included in the one-centre retrospective study. Data are presented as median (25th, 75th percentile). RESULTS: The median age was 27 (23; 29) years. Among the patients, there were 4 (19%) cases of idiopathic PAH and in 17 (81%) women PAH was associated with congenital heart disease (CHD); 12 (57%) patients'demonstrated Eisenmenger syndrome. Baseline SPAP was 90 (82; 103) mm Hg. SpO2 90 (85,95)%. All women taken PAH-specific therapy (sildenafil) before delivery. Caesarean section (CS) were performed at 32 (28; 34) weeks. In 20 cases CS was perfofined under epidural anesthesia and in one case under general anesthesia due thrombocytopenia. Inhaled nitric oxide (NO) was administered intraoperative to all women in a dose of 40-60 ppm. Postoperative period was uncomplicated in five women (23?8%). Decompensation with PAP rise, acute right ventricular failure and hypoxemia developed in 16 (76,2%) cases 30 (24, 40) h after abdominal delivery. These patients required combined PAH-specific therapy (NO, sldenafil, iloprost) and inotropic agents, additionallyrespiratory support was used in four patients. The median ICU stay was 13 (9; 22) days. 3 patients died (14?2%); mortality in Eisenmenger syndrome cases was 25% (3/12). 18 healthy babies.


Asunto(s)
Anestesia por Inhalación/métodos , Cesárea , Cuidados Críticos/métodos , Hipertensión Pulmonar/cirugía , Complicaciones del Embarazo/cirugía , Adulto , Femenino , Humanos , Hipertensión Pulmonar/etiología , Hipertensión Pulmonar/mortalidad , Monitoreo Intraoperatorio , Periodo Perioperatorio , Embarazo , Complicaciones del Embarazo/etiología , Resultado del Embarazo , Respiración Artificial , Estudios Retrospectivos , Resultado del Tratamiento
4.
Biomed Khim ; 65(1): 57-62, 2019 Jan.
Artículo en Ruso | MEDLINE | ID: mdl-30816098

RESUMEN

The mechanism of valve calcification that is the main cause of aortic stenosis formation and progression is not yet clear. In recent years, the role of the OPG/RANKL/RANK system is considered as one of possible variants of pathogenesis of valve calcification. In presented work the differences in OPG and sRANKL levels involved in the calcification processes in tissues of patients with severe aortic stenosis have been examined. The study was performed using three groups of patients: group 1 - patients with aortic stenosis, group 2 - patients with aortic aneurysm, and group 3 - patients with aortic stenosis and aortic dilatation. In patients with aortic stenosis, the level of RANKL was significantly higher, and the level of RANKL was higher in valve than in tissue. The negative correlation between aortic dilatation and RANKL level indicated the lack of RANKL influence on pathogenesis of aortic dilatation. The obtained data confirm the increased expression of RANKL in patients with aortic valve calcification. The results of this study confirm importance of the OPG/RANKL/RANK system in calcification in patients with aortic stenosis. Athough patients of all groups had comparable values of OPG (including patients with aortic dilatation), the RANKL level increased only in patients with aortic stenosis. This suggest involvement of some additional mechanisms influencing the increase of RANKL expression.


Asunto(s)
Estenosis de la Válvula Aórtica , Calcinosis/metabolismo , Osteoprotegerina/metabolismo , Ligando RANK/metabolismo , Válvula Aórtica/patología , Humanos , Receptor Activador del Factor Nuclear kappa-B/metabolismo
5.
Biomed Khim ; 62(2): 198-205, 2016.
Artículo en Ruso | MEDLINE | ID: mdl-27143380

RESUMEN

The level of peroxisome proliferator-activated receptor gamma coactivator-1alpha (PGC1α) in human blood plasma was investigated. Samples of healthy individuals (n=34) and patients with cardiovascular diseases (n=110), including aortic aneurysm (n=69), aortic stenosis (n=25) and patients without aortic pathologies were analyzed. In patients the PGC1α concentration was higher than that in healthy persons, and tended to decrease with age. Elevated concentrations of lactic acid, total homocysteine and asymmetric dimethylarginine in the blood of patients suggested a parallel development of endothelial and secondary mitochondrial dysfunction. However, concentrations of lactic and pyruvic acids exceeding reference limit were associated with the decrease in the PGC1α level.


Asunto(s)
Enfermedades Cardiovasculares/sangre , Factores de Transcripción/sangre , Factores de Edad , Aneurisma de la Aorta/sangre , Estenosis de la Válvula Aórtica/sangre , Arginina/análogos & derivados , Arginina/sangre , Biomarcadores/sangre , Estudios de Casos y Controles , Endotelio Vascular/metabolismo , Endotelio Vascular/fisiopatología , Femenino , Homocisteína/sangre , Humanos , Ácido Láctico/sangre , Masculino , Persona de Mediana Edad , Óxidos de Nitrógeno/sangre , Coactivador 1-alfa del Receptor Activado por Proliferadores de Peroxisomas gamma , Ácido Pirúvico/sangre
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