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1.
Acta Anatomica Sinica ; (6): 225-230, 2021.
Artigo em Chinês | WPRIM | ID: wpr-1015479

RESUMO

Objective To investigate the protective effect of nuclear factor E2-related factor 2(Nrf2)on hydrogen peroxide (H

2.
Chinese Medical Journal ; (24): 1302-1309, 2013.
Artigo em Inglês | WPRIM | ID: wpr-342185

RESUMO

<p><b>BACKGROUND</b>Our previous studies have indicated that the beneficial effects of grafting neural stem cells (NSCs) overexpressing glial cell line-derived neurotrophic factor (GDNF) in rats after stroke. However, the underlying mechanisms are highly debatable. In this study, we investigated whether neurogenesis, Akt, and extracellular signal-regulated kinase 1/2 (Erk1/2) signaling were involved in this process.</p><p><b>METHODS</b>Transient ischemic stroke were induced by occluding middle cerebral artery for 2 hours and reperfusion. At 3 days after reperfusion, GDNF/NSCs, NSCs, and vehicle were administered. Immunohistochemical staining was used to evaluate neurogenesis by nestin antibody; phosphorylation of Akt and Erk1/2 was investigated by Western blotting analysis.</p><p><b>RESULTS</b>Transplantation of GDNF/NSCs and NSCs significantly increased nestin-positive cells compared to control group (vehicle) from 1 to 7 weeks after reperfusion, and GDNF/NSCs showed stronger effect than NSCs at 2 and 3 weeks after reperfusion. Meanwhile, enhanced phosphorylation level of Erk1/2 was observed in the GDNF/NSCs and NSCs groups compared with control group, and phosphorylation level of Erk1/2 in GDNF/NSCs group was remarkably higher than that of NSCs group at any given time. In contrast, expression of mitogen-activated protein kinase phosphatase-1 (MKP-1), known as inhibitor of Erk1/2 signaling, was significantly decreased in the GDNF/NSCs and NSCs groups compared with the control group. Moreover, much enhanced and prolonged phosphorylation level of Akt of GDNF/NSCs group was detected compared with control and NSCs group.</p><p><b>CONCLUSION</b>Grafting GDNF/NSCs enhances neurogenesis and activates Akt and Erk1/2 signaling, that may provide the potential for GDNF/NSCs in stroke treatment.</p>


Assuntos
Animais , Masculino , Ratos , Fator Neurotrófico Derivado de Linhagem de Célula Glial , Metabolismo , Proteína Quinase 1 Ativada por Mitógeno , Metabolismo , Proteína Quinase 3 Ativada por Mitógeno , Metabolismo , Células-Tronco Neurais , Biologia Celular , Metabolismo , Neurogênese , Fisiologia , Fosforilação , Proteínas Proto-Oncogênicas c-akt , Metabolismo , Ratos Sprague-Dawley , Transplante de Células-Tronco , Acidente Vascular Cerebral , Metabolismo , Terapêutica
3.
Chinese Journal of Medical Instrumentation ; (6): 328-331, 2009.
Artigo em Chinês | WPRIM | ID: wpr-329313

RESUMO

<p><b>OBJECTIVE</b>To explore the possibility of clinical evaluation of cardiac function by CHM T3002 non-invasive hemodynamic monitor.</p><p><b>METHODS</b>A total of 26 patients admitted to Zhongshan Hospital in Shanghai were enrolled, including 11 cardiac insufficiency patients and 15 control. Each subject was tested by non-invasive cardiac hemodynamic monitor immediately after echocardiography. Linear regression analysis and Bland-Altman consistency analysis were used in the analysis of relevance and consistency between two different methods.</p><p><b>RESULTS</b>Linear correlation was shown on LVEF, SV, SVI, CO, CI, EDV, LVET and PEP/LVET, but not on PEP, between the two methods. Moreover, the consistency of the two methods was highly confirmed on LVEF and LVET, less on SV, SVI, CO, CI and EDV, while awfully weak on PEP and PEP/LVET.</p><p><b>CONCLUSION</b>CHM T3002 non-invasive hemodynamic monitor may be useful in assessing patients' cardiac function, however, it can not replace cardiac echocardiography.</p>


Assuntos
Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos de Casos e Controles , Ecocardiografia , Desenho de Equipamento , Hemodinâmica , Monitorização Fisiológica
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