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1.
Zhejiang Da Xue Xue Bao Yi Xue Ban ; 53(2): 244-253, 2024 Apr 25.
Artigo em Inglês, Chinês | MEDLINE | ID: mdl-38594961

RESUMO

Induced pluripotent stem cells (iPSCs) are obtained by introducing exogenous genes or adding chemicals to the culture medium to induce somatic cell differentiation. Similarly to embryonic stem cells, iPSCs have the ability to differentiate into all three embryonic cell lines. iPSCs can differentiate into cardiac muscle cells through two-dimensional differentiation methods such as monolayer cell culture and co-culture, or through embryoid body and scaffold-based three-dimensional differentiation methods. In addition, the process of iPSCs differentiation into cardiac muscle cells also requires activation or inhibition of specific signaling pathways,such as Wnt, BMP, Notch signaling pathways to mimic the development of the heart in vivo. In recent years, suspension culturing in bioreactors has been shown to produce large number of iPSCs derived cardiac muscle cells (iPSC-CMs). Before transplantation, it is necessary to purify iPSC-CMs through metabolic regulation or cell sorting to eliminate undifferentiated iPSCs, which may lead to teratoma formation. The transplantation methods for iPSC-CMs are mainly injection of cell suspension and transplantation of cell patches into the infarcted myocardium. Animal studies have shown that transplantation of iPSC-CMs into the infarcted myocardium can improve cardiac function. This article reviews the progress in preclinical studies on iPSC-CMs therapy for acute myocardial infarction and discusses the limitations and challenges of its clinical application to provide references for further clinical research and application.


Assuntos
Diferenciação Celular , Células-Tronco Pluripotentes Induzidas , Infarto do Miocárdio , Células-Tronco Pluripotentes Induzidas/citologia , Infarto do Miocárdio/terapia , Humanos , Animais , Miócitos Cardíacos/citologia , Transplante de Células-Tronco/métodos
2.
ACS Omega ; 9(7): 8381-8396, 2024 Feb 20.
Artigo em Inglês | MEDLINE | ID: mdl-38405452

RESUMO

In view of the problems of low liquid production, a high proportion of high water cut wells, and poor development effect in the late stage of water flooding in the special sandstone reservoir of Niuquanhu "low permeability and medium viscosity crude oil", we carried out the research on hydrocarbon gas oil recovery and its influencing factors. First, the influence of different injected gas media on the physical properties of crude oil was analyzed. Second, the core displacement experiments of different gas injection media including CO2, CH4, and hydrocarbon gas were carried out by using the method of oil recovery comparison and optimization. Third, the indoor experimental study on the oil recovery of different influencing factors was carried out by using the method of controlling variables of influencing factors. Finally, the influence degree of different influencing factors on oil recovery was analyzed by a Spearman rank correlation coefficient analysis. The experimental results showed that the oil recovery of hydrocarbon gas is higher than that of CO2 and CH4, which were 57, 51, and 18% respectively. This is mainly because hydrocarbon gas is similar to the components of crude oil and is more easily dissolved in crude oil. The experimental results of influencing factors showed that the higher the content of C2-C4, the higher the oil recovery, and the content of C2-C4 will affect its dissolution with crude oil and its interaction with heavy component crude oil. The larger the permeability ratio, the lower the oil recovery, which was mainly due to the uneven distribution of injected gas in different regions. The higher the permeability, the lower the oil recovery, which was also due to the serious heterogeneity of the low permeability core of Niuquanhu; The results of Spearman rank correlation coefficient analysis based on different influencing factors and oil recovery showed that the order of influence of different factors on oil recovery was C2-C4 content > permeability ratio > permeability > back pressure > gas injection rate. In the development process of hydrocarbon gas injection, we should control the C2-C4 content, back pressure, and injection rate. The research in this study not only provides theoretical support for gas injection enhanced oil recovery technology in "low permeability and medium viscosity crude oil" reservoirs but also provides a new idea for the ranking of influencing factors.

3.
Mar Drugs ; 20(9)2022 Sep 13.
Artigo em Inglês | MEDLINE | ID: mdl-36135764

RESUMO

Four undescribed phenolic compounds, namely asperpropanols A-D (1-4), along with two known congeners 5 and 6, were isolated from Aspergillus puniceus A2, a deep-sea-derived fungus. The gross structures of the compounds were established by detailed analyses of the HRESIMS and NMR data, and their absolute configurations were resolved by modified Mosher's method and calculations of ECD data. Compounds 1-6 were found to have excellent anti-inflammatory effect on lipopolysaccharide (LPS)-induced RAW264.7 cells at 20 µM, evidenced by the reduced nitric oxide (NO), tumor necrosis factor α, and interleukin 6 production. Among them, 5 and 6 showed inhibitory effects on NO production comparable with the positive control (BAY11-7083 at 10 µM). Additionally, the LPS-induced mRNA expressions of inducible nitric oxide synthase and cyclooxygenase-2 were also decreased. Interestingly, mRNA expression of nuclear factor erythroid 2-related factor 2 (Nrf2) was downregulated by LPS and recovered by 1-6, suggesting a vital role of Nrf2 in their effect. We further found that pharmacological inhibition of Nrf2 by ML385 largely abrogated the effects of 1-6 on RAW264.7 cells. Therefore, 1-6 may share a common anti-inflammatory mechanism via Nrf2 upregulation and activation.


Assuntos
Lipopolissacarídeos , Fator 2 Relacionado a NF-E2 , Anti-Inflamatórios/química , Anti-Inflamatórios/farmacologia , Aspergillus , Ciclo-Oxigenase 2/metabolismo , Fungos/química , Heme Oxigenase-1/metabolismo , Interleucina-6/metabolismo , Lipopolissacarídeos/farmacologia , Fator 2 Relacionado a NF-E2/metabolismo , Óxido Nítrico/metabolismo , Óxido Nítrico Sintase Tipo II/metabolismo , Fenóis/farmacologia , RNA Mensageiro , Fator de Necrose Tumoral alfa/metabolismo
4.
Zhonghua Yi Xue Za Zhi ; 88(32): 2299-301, 2008 Aug 19.
Artigo em Chinês | MEDLINE | ID: mdl-19087684

RESUMO

OBJECTIVE: To observe the pharmacokinetics of adriamycin-adsorbing nanometric activated carbon in intralymphatic chemotherapy. METHODS: Two ml of suspension of activated carbon with the diameter of 21 nm was mixed with adriamycin 5 mg. Eighteen dogs were randomly divided into 6 equal groups. The above mentioned mixture was injected subserosally to the anterior wall of gastric antrum of the dogs. Thirty minutes, 1 h, 2 h, 1 day, and 3 days after the injection the gastroepiploic lymph nodes of the Groups 1 - 5 were obtained. And Group 6 underwent extraction of venous blood samples 5, 15, 30, 60, 120, and 240 minutes after the injection and extraction of thoracic duct fluid 5, 15, 30, 60, 120, 240, and 360 minutes after the injection. The adriamycin concentrations at different time points were determined by mass spectrometer. The lymphatic vessels and nodes at the gastric wall were observed by the naked eyes. RESULTS: Black tiny lymphatic vessels and lymph nodes were visualized around the injection areas immediately after the injection. Adriamycin content could be detected 30 min after the injection and lasted for 72 h at high levels with the peak content of (84.6 +/- 2.0) microg per gram tissue at 60 min in the perilymph node of gastroepiploic artery. The adriamycin concentration in the lymph fluid of thoracic duct reached the top level of 162.5 ng/ml 30 min after the injection, and then decreased slowly. Adriamycin could be still detected in lymph fluid 6 h after injection. No trace of adriamycin was found in the blood at any time points. CONCLUSION: The content of adriamycin can keep high and last long in the drainage of lymph node and lymph fluid in the treatment of intralymphatic chemotherapy using adriamycin-adsorbing nanometric activated carbon.


Assuntos
Doxorrubicina/farmacocinética , Linfonodos/metabolismo , Animais , Antibióticos Antineoplásicos/administração & dosagem , Antibióticos Antineoplásicos/química , Antibióticos Antineoplásicos/farmacocinética , Carvão Vegetal/química , Cães , Doxorrubicina/administração & dosagem , Doxorrubicina/química , Sistemas de Liberação de Medicamentos/métodos , Espectrometria de Massas , Nanotubos de Carbono/química , Distribuição Aleatória
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