Search

Gas and water migration through the hydrate-bearing sediment are characteristic features in marine gas hydrate reservoirs worldwide. However, there are few experimental investigations on the effect of water-gas flow on the gas hydrate reservoir. In this study, gas-water migration in gas hydrate stability zone (GHSZ) was investigated visually employing a high-resolution magnetic resonance imaging (MRI) apparatus, and the formation of hydrate seal was experimentally investigated. Results revealed that normal flow of gas-water at the low flow rate of 1–0.25 mL/min will induce the hydrate reformation. Conversely, higher gas-water flow rates (at 2–0.5 and 4–1 mL/min) need higher reservoir pressure to induce the hydrate reformation. In addition, the hydrate reformation during the gas-water flow process produced the hydrate seal, which can withstand an over 9.0 MPa overpressure. This high overpressure provides the development condition for the underlying gas and/or water reservoir. A composite MRI image of the whole hydrate seal was obtained through the MRI. The pore difference between hydrate zone and coexistence zone produces a capillary sealing effect for hydrate seal. The hydrate saturation of hydrate seal was more than 51.6%, and the water saturation was more than 19.3%. However, the hydrate seal can be broken through when the overpressure exceeded the capillary pressure of the hydrate seal, which induced the sudden drop of reservoir pressure. This study provides a scientific explanation for the existence of high-pressure underlying gas below the hydrate layer and is significant for the safe exploitation of these common typical marine hydrate reservoirs. [ABSTRACT FROM AUTHOR]

Aim: The study aims to evaluate protective effects of sophoricoside (Sop) on cardiac hypertrophy. Meanwhile, the potential and significance of Sop should be broadened and it should be considered as an attractive drug for the treatment of pathological cardiac hypertrophy and heart failure. Methods: Using the phenylephrine (PE)-induced neonatal rat cardiomyocytes (NRCMs) enlargement model, the potent protection of Sop against cardiomyocytes enlargement was evaluated. The function of Sop was validated in mice received transverse aortic coarctation (TAC) or sham surgery. At 1 week after TAC surgery, mice were treated with Sop for the following 4 weeks, the hearts were harvested after echocardiography examination. Results: Our study revealed that Sop significantly mitigated TAC-induced heart dysfunction, cardiomyocyte hypertrophy and cardiac fibrosis. Mechanistically, Sop treatment induced a remarkable activation of AMPK/mTORC1-autophagy cascade following sustained hypertrophic stimulation. Importantly, the protective effect of Sop was largely abolished by the AMPKa inhibitor Compound C, suggesting an AMPK activation-dependent manner of Sop function on suppressing pathological cardiac hypertrophy. Conclusion: Sop ameliorates cardiac hypertrophy by activating AMPK/mTORC1-mediated autophagy. Hence, Sop might be an attractive candidate for the treatment of pathological cardiac hypertrophy and heart failure. [ABSTRACT FROM AUTHOR]

Diversity and plasticity are the hallmarks of cells from the monocyte-macrophage lineage. Macrophages undergo classical M1 or alternative M2 activation in response to the microenvironment signals. Several transcription factors, such as peroxisome proliferator-activated receptors, signal transducers and activators of transcription, CCAAT-enhancer-binding proteins, interferon regulatory factors, Kruppel-like factors, GATA binding protein 3, nuclear transcription factor-κB, and c-MYC, were found to promote the expression of specific genes, which dictate the functional polarization of macrophages. Importantly, these transcription factors can be regulated by microRNAs (miRNAs), a group of small non-coding RNAs, which regulate gene expression through translation repression or mRNA degradation. Recent studies have also revealed that miRNAs control macrophage polarization by regulating transcription factors in response to the microenvironment signals. This review will summarize recent progress of miRNAs in the transcriptional regulation of macrophage polarization and provide the insights into the development of macrophage-centered diagnostic and therapeutic strategies. [ABSTRACT FROM AUTHOR]

Aim:To determine the effects and potential mechanisms of ibrolipim on ATP-binding membrane cassette transporter A-1 (ABCA1) and ATP-binding membrane cassette transporter G-1 (ABCG1) expression from human macrophage foam cells, which may play a critical role in atherogenesis.Methods:Human THP-1 cells pre-incubated with ox-LDL served as foam cell models. Specific mRNA was quantified using real-time RT-PCR and protein expression using Western blotting. Cellular cholesterol handling was studied using cholesterol efflux experiments and high performance liquid chromatography assays.Results:Ibrolipim 5 and 50 μmol/L significantly increased cholesterol efflux from THP-1 macrophage-derived foam cells to apoA-I or HDL. Moreover, it upregulated the expression of ABCA1 and ABCG1. In addition, LXRα was also upregulated by the ibrolipim treatment. In addition, LXRα small interfering RNA completely abolished the promotion effect that was induced by ibrolipim.Conclusion:Ibrolipim increased ABCA1 and ABCG1 expression and promoted cholesterol efflux, which was mediated by the LXRα signaling pathway. [ABSTRACT FROM AUTHOR]