Untargeted lipidomics of bronchopulmonary dysplasia induced by hyperoxia exposure in rats.

Background: Bronchopulmonary dysplasia (BPD), characterized by impaired lung development, remains a leading cause of morbidity and mortality in premature infants. The synthesis and metabolism of lipids play a critical role in normal lung development, such as dipalmitoylphosphatidylcholine, a key component of pulmonary surfactant (PS). Therefore, we conducted a lipidomics study of rat lung tissue to explore the changes of pulmonary lipid composition in the progression of BPD disease. Methods: In this study, we exposed neonatal Sprague-Dawley (SD) rats to hyperoxia for 14 days. After hyperoxia exposure, the lung tissues of rats were analyzed pathologically, and untargeted lipidomics was analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Results: Hematoxylin-eosin (H&E) staining showed that the alveoli enlarged, the number of alveoli decreased and the pulmonary surfactant-associated protein D (SFTPD) decreased in hyperoxia-exposed rats. A total of 620 pulmonary lipids were detected by LC-MS/MS, covering 27 lipid categories. The most common lipids were triacylglycerol (TAG), followed by phosphatidylcholine (PC) and phosphatidylethanolamine (PE). Conclusions: Compared with those rats exposed to normoxic conditions, the lipid levels in the lungs of rats exposed to hyperoxia for 14 days generally decreased, with the levels of TAG and PC decreasing most significantly. In short, our results provide a clue for finding therapeutic targets and biomarkers of a BPD rat model lung liposome.

PC (16:0/14:0) ameliorates hyperoxia-induced bronchopulmonary dysplasia by upregulating claudin-1 and promoting alveolar type II cell repair.

Bronchopulmonary dysplasia (BPD) remains a significant challenge in neonatal care, the pathogenesis of which potentially involves altered lipid metabolism. Given the critical role of lipids in lung development and the injury response, we hypothesized that specific lipid species could serve as therapeutic agents in BPD. This study aimed to investigate the role of the lipid Phosphatidylcholine (PC) (16:0/14:0) in modulating BPD pathology and to elucidate its underlying mechanisms of action. Our approach integrated in vitro and in vivo methodologies to assess the effects of PC (16:0/14:0) on the histopathology, cellular proliferation, apoptosis, and molecular markers in lung tissue. In a hyperoxia-induced BPD rat model, we observed a reduction in alveolar number and an enlargement in alveolar size, which were ameliorated by PC (16:0/14:0) treatment. Correspondingly, in BPD cell models, PC (16:0/14:0) intervention led to increased cell viability, enhanced proliferation, reduced apoptosis, and elevated surfactant protein C (SPC) expression. RNA sequencing revealed significant gene expression differences between BPD and PC (16:0/14:0) treated groups, with a particular focus on Cldn1 (encoding claudin 1), which was significantly enriched in our analysis. Our findings suggest that PC (16:0/14:0) might protect against hyperoxia-induced alveolar type II cell damage by upregulating CLDN1 expression, potentially serving as a novel therapeutic target for BPD. This study not only advances our understanding of the role of lipids in BPD pathogenesis, but also highlights the significance of PC (16:0/14:0) in the prevention and treatment of BPD, offering new avenues for future research and therapeutic development.

Human milk exosome-derived circDNAJB6 improves bronchopulmonary dysplasia model by promoting DNAJB6 gene transcription.

To verify the protective effect of circDNAJB6 on Bronchopulmonary dysplasia (BPD) cell and animal models and to explore the possible mechanism of its protective effect. The function of circDNAJB6 was investigated at the cell and animal levels. Nuclear and Cytoplasmic RNA extraction kits and fluorescence in situ hybridization (FISH) were used to explore the distribution of circDNAJB6 in cells, and the potential mechanism of circDNAJB6 was verified by q-PCR, luciferase assays and rescue experiments.CircDNAJB6 is abundant in breast milk exosomes. Overexpression of circDNAJB6 can ameliorate damage in BPD models caused by hyperoxia exposure in vivo and in vitro. Mechanistically, circDNAJB6 can target the downstream DNAJB6 gene and promote the transcription of DNAJB6, exertive a protective effect on the experimental BPD model. Our results showed that circDNAJB6 alleviated damage and inhibited the proliferation of alveolar epithelial cells in the BPD model by promoting transcription of parent gene DNAJB6. Human milk exosome-derived circDNAJB6 provides new directions for preventing and treating BPD.

Frictional properties of MoS2 on a multi-level rough wall under starved lubrication.

Owing to nano-MoS2's excellent anti-friction and anti-wear properties, nano-MoS2, which can act as a nano-additive in lubricating oil or solid lubricants, is believed to have great potential in the lubrication of power machinery and moving parts of a spacecraft. The molecular dynamics method was used to construct a rough surface and a multi-level asperity structure to simulate starved lubrication before oil film breakdown, and the lubrication mechanism of MoS2 as a nano-additive or directly coated on the textured surface could reduce the friction coefficient and wear was explained from the atomic perspective. Simulations showed that the multilayer MoS2 played a role of load-bearing at light load or low velocity, and slipped into the grooves to repair the surface under heavy load or high velocity. Even if local asperity contact occurs, MoS2 nanoparticles could accelerate the detachment of the initial asperity contact to prevent large-scale adhesion. The MoS2 nanoparticles transformed the pure liquid oil film into a liquid-solid composite oil film, which was more suitable for lubrication under heavy load and high velocity because it increased the contact area, protected the friction surface and prevented asperity contact. The proposed lubrication mechanism contributes to understanding the frictional properties of layered nanomaterials under extreme conditions and provides a reference for further application of MoS2 materials in the field of lubrication.

Research on the Impact Mechanical Properties of Real-Time High-Temperature Granite and a Coupled Thermal-Mechanical Constitutive Model.

Studying the mechanical behavior of rocks under real-time high-temperature conditions is of great significance for the development of energy caverns, nuclear waste disposal projects, and tunneling engineering. In this study, a real-time high-temperature impact compression test was conducted on Sejila Mountain granite to explore the effects of temperature and external load on its mechanical properties. Based on the concepts of damage mechanics and statistics, a coupled thermal-mechanical (T-M) damage constitutive model was established, which considers the temperature effect and uses the double-shear unified strength as the yield criterion. The parameter expressions were clarified, and the accuracy and applicability of the model were verified by experimental data. The research results indicated that high temperatures had an obvious damaging and deteriorating effect on the strength of the granite, while an increase in impact velocity had an enhancing effect on the strength of the granite. The established constitutive model theoretical curve and test curve showed a high degree of agreement, indicating that the coupled T-M model can objectively represent the evolution process of damage in rocks and the physical meaning of its parameters is clear.

Human breast milk-derived exosomes through inhibiting AT II cell apoptosis to prevent bronchopulmonary dysplasia in rat lung.

Human breast milk (HBM) effectively prevents and cures neonatal bronchopulmonary dysplasia (BPD). Exosomes are abundant in breast milk, but the function of HBM-derived exosomes (HBM-Exo) in BPD is still unclear. This study was to investigate the role and mechanism of HBM-Exo in BPD. Overall lung tissue photography and H&E staining showed that HBM-Exo improved the lung tissue structure collapse, alveolar structure disorder, alveolar septum width, alveolar number reduction and other injuries caused by high oxygen exposure. Immunohistochemical results showed that HBM-Exo improved the inhibition of cell proliferation and increased apoptosis caused by hyperoxia. qPCR and Western blot results also showed that HBM-Exo improved the expression of Type II alveolar epithelium (AT II) surface marker SPC. In vivo study, CCK8 and flow cytometry showed that HBM-Exo improved the proliferation inhibition and apoptosis of AT II cells induced by hyperoxia, qPCR and immunofluorescence also showed that HBM-Exo improved the down-regulation of SPC. Further RNA-Seq results in AT II cells showed that a total of 88 genes were significantly different between the hyperoxia and HBM-Exo with hyperoxia groups, including 24 up-regulated genes and 64 down-regulated genes. KEGG pathway analysis showed the enrichment of IL-17 signalling pathway was the most significant. Further rescue experiments showed that HBM-Exo improved AT II cell damage induced by hyperoxia through inhibiting downstream of IL-17 signalling pathway (FADD), which may be an important mechanism of HBM-Exo in the prevention and treatment of BPD. This study may provide new approach in the treatment of BPD.

Exposure to Polybrominated Diphenyl Ethers in the Sixth Total Diet Study - China, 2016-2019.

What is already known about this topic?: Polybrominated diphenyl ethers (PBDEs) were widely used in many industrial and commercial materials as flame retardants, and its related exposure threatens human health. What is added by this report?: The Sixth Total Diet Study (TDS) indicated that the dietary intake of PBDEs was unlikely to pose significant health risks for the general Chinese people using the margin of exposure (MOE) approach recommended by the European Food Safety Authority (EFSA). What are the implications for public health practice?: This study highlights the necessity of continuous national monitoring of the dietary intake and strict legislation of PBDEs in China.

Dynamic Mechanical Properties and Visco-Elastic Damage Constitutive Model of Freeze-thawed Concrete.

To study the dynamic mechanical characteristics and constitutive relation of concrete materials under freeze-thaw (FT) cycle conditions, C35 concrete was taken as the research object in this paper, and FT tests were carried out with a freeze-thaw range of -20-20 °C and a freeze-thaw frequency up to 50 times. By using the separated Hopkinson pressure bar (SHPB) system, impact compression tests of concrete specimens under different FT cycle actions were developed, then the dynamic fracture morphology, fracture block distribution, stress-strain curve, peak stress and other dynamic mechanical properties of concrete were analyzed, and the influence law of FT action and strain rate was obtained. Through introducing the freeze-thaw deterioration damage factor and the stress damage variable, the dynamic visco-elastic damage constitutive equation of freeze-thawed concrete was constructed based on component combination theory. Furthermore, the damage evolution process and mechanism of freeze-thawed concrete materials were revealed. The research results show that the dynamic mechanical properties of concrete under a freeze-thaw environment are the combined results of the freeze-thaw deterioration effect and the strain rate strengthening effect. The dynamic visco-elastic damage constitutive model established in this paper can effectively describe the dynamic mechanical properties of freeze-thawed concrete, and has the characteristics of few parameters and good effect. The stress damage evolution path of concrete goes backward with the increase of FT cycles and the development speed gradually slows down. The greater the difference in FT cycles, the greater the difference in stress damage path.

Impact Compression Test and Numerical Simulation Analysis of Concrete after Thermal Treatment in Complex Stress State.

To study the dynamic mechanical properties and fracture law of concrete after thermal treatment and reveal its mechanism, the impact compression test was carried out on different thermal-treated (400-800 °C) concrete specimens using a split Hopkinson pressure bas (SHPB) system. By using ANSYS/LS-DYNA, the finite element numerical simulation of the test process was illustrated. The research showed that under passive confining pressure, the more the loading rate is increased, the more obvious the effect of the passive confining pressure on the concrete specimen, as well as the more significant the improvement of the peak stress compared with the uniaxial test. On the other hand, as the temperature damage effect is enhanced, the increase in the material strength at different loading rates is reduced. Numerical simulations showed that in a uniaxial test, as the impact rate increases, the crack initiation time advances, and the degree of fracture increases at the same rate as that of the loading time. In the case of confining pressure, the stress gradually decreases to the edge from the center, and has a significant circumferential diffusion characteristic. The circumferential restraint of the passive confining pressure limits the radial deformation ability of the material to a certain extent, thereby increasing the axial compressive strength. In the analysis of the crushing process of concrete specimens, it was found that the fracture form showed a strong rate dependence. When the loading rate is low, the fracture form is a cleavage-like failure. As the loading rate increases, the fracture form changes to crush failure. The research results provide the necessary theoretical basis for the safety assessment, reinforcement, and maintenance of concrete structures after fire.

Research on the Impact Loading and Energy Dissipation of Concrete after Elevated Temperature under Different Heating Gradients and Cooling Methods.

To provide theoretical basis for fire rescue, post-disaster safety evaluation, and reinforcement of concrete structures, C35 concrete materials are treated with high-temperature heating (200 °C, 400 °C, 600 °C, 800 °C) under two different heating gradients. After natural cooling and water cooling to normal temperature, an impact compression test was carried out at different loading rates using a Split Hopkinson Pressure Bar (SHPB) system with a diameter of 100 mm, and finally the crushed specimens were subjected to a sieving test. The effects of elevated temperatures, cooling methods, heating gradients, and loading rates on the fragment size distribution, fractal characteristics, and energy dissipation of impact-compressed concrete specimens were studied. The results show that with the increase of the loading rate and the rise of the heating temperature, the crushing degree of concrete specimens gradually increases, the average fragment size decreases, and the mass distribution of the fragments move from the coarse end to the fine end. The fragment size distribution of the specimen has obvious fractal characteristics. In addition, its fractal dimension increases with the increase of loading rate and heating temperature, the average size of the specimen fragments decreases correspondingly, and the fracture of the specimen becomes more serious. When the different heating gradients were compared, it was found that the fractal dimension of the specimens subjected to rapid heating treatment was larger than that of the slow heating treatment specimens, and the crushing degree of the specimens with different cooling methods was discrete. By analyzing the energy dissipation of the specimen under different conditions, it is shown that both the fractal dimension and the peak stress increase with the increase of the fragmentation energy dissipation density. It shows that there is a close correlation between the change of fractal dimension and its macroscopic dynamic mechanical properties.