A Quantitative Rating System for Pollutant Emission Reduction of Asphalt Mixture

This study presents a comprehensive pollutant reduction rating system for hot mix asphalt (HMA) with three Level I indices and ten Level II indices, covering various aspects in HMA pollutant emissions, energy consumption, and exhausts from construction equipment. The pollutant emission reduction effects are investigated not only in the laboratory for modified asphalt mixtures with various mixture gradation and binder types but also in the field for several warm mix asphalt (WMA) projects. Furthermore, energy consumption and emission data during pavement construction are obtained from 58 in situ highway projects in 10 provinces of China. Based on the hierarchical clustering method and Bayesian discriminant analysis, individual ranking systems are developed to quantify pollutant emission reduction effects and energy consumption. Subsequently, a comprehensive reduction rating system is established based on the analytic hierarchy process and approximation methods. A case study is demonstrated to implement the proposed system for the assessment of emission reduction effects

Molecular-size dependence of glycogen enzymatic degradation and its importance for diabetes

Glycogen, a hyperbranched glucose polymer, is the blood-sugar reservoir in animals. Liver glycogen comprises small β particles, which can join together as large composite α particles. It had been shown that the binding between β in α particles in the liver of diabetic mice is more fragile than in healthy mice. This could be linked to the loss of blood-sugar control characteristic of diabetes if the rate per monomer unit of the enzymatic degradation to glucose of α particles were significantly slower than that of β particles. This is tested here by examining the in vitro time evolution of the molecular size distribution of glycogen from the livers of healthy and diabetic mice and rats, containing distinct components of both α and β particles; this treatment is analogous to the “competitive growth” method used to explore mechanisms in emulsion polymerization. Simulations for the time evolution of the molecular size distribution were also performed. It is found that the degradation rate per monomer unit is indeed faster for the smaller particles, supporting the hypothesis of a causal link between chemical fragility of glycogen from diabetic liver with poor control of blood-sugar release. Comparison between simulations and experiment indicate that α and β particles have significant structural differences

Implications for biological function of lobe dependence of the molecular structure of liver glycogen

Liver glycogen, a complex branched polymer of glucose, plays a major role in controlling blood-sugar levels. Understanding its molecular structure is important for diabetes, especially since it has been found that this structure is more fragile in diabetic than in healthy mouse liver. However, there are differences in metabolic processes between liver lobes, which would be expected to be reflected in differing glycogen molecular structures. This structure was examined for separated lobe regions in rat livers, using size-exclusion chromatography (SEC) and fluorophore-assisted carbohydrate electrophoresis. The results show that the SEC weight distribution of glycogen, and the molecular weight distribution of individual branches (chains), from different lobes are similar. This shows that (a) molecular structural characterization of glycogen from whole-liver biopsy is representative (which is convenient because the commonest animal model for diabetes is the mouse, whose livers are very small), and (b) the fact that molecular structure is conserved (regulated) in different lobes suggests that this structure plays an important role in blood-sugar regulation

The mechanisms of Yu Ping Feng San in tracking the cisplatin-resistance by regulating ATP-binding cassette transporter and glutathione S-transferase in lung cancer cells

Cisplatin is one of the first line anti-cancer drugs prescribed for treatment of solid tumors; however, the chemotherapeutic drug resistance is still a major obstacle of cisplatin in treating cancers. Yu Ping Feng San (YPFS), a well-known ancient Chinese herbal combination formula consisting of Astragali Radix, Atractylodis Macrocephalae Rhizoma and Saposhnikoviae Radix, is prescribed as a herbal decoction to treat immune disorders in clinic. To understand the fast-onset action of YPFS as an anti-cancer drug to fight against the drug resistance of cisplatin, we provided detailed analyses of intracellular cisplatin accumulation, cell viability, and expressions and activities of ATP-binding cassette transporters and glutathione S-transferases (GSTs) in YPFS-treated lung cancer cell lines. In cultured A549 or its cisplatin-resistance A549/DDP cells, application of YPFS increased accumulation of intracellular cisplatin, resulting in lower cell viability. In parallel, the activities and expressions of ATP-binding cassette transporters and GSTs were down-regulated in the presence of YPFS. The expression of p65 subunit of NF-κB complex was reduced by treating the cultures with YPFS, leading to a high ratio of Bax/Bcl-2, i.e. increasing the rate of cell death. Prim-O-glucosylcimifugin, one of the abundant ingredients in YPFS, modulated the activity of GSTs, and then elevated cisplatin accumulation, resulting in increased cell apoptosis. The present result supports the notion of YPFS in reversing drug resistance of cisplatin in lung cancer cells by elevating of intracellular cisplatin, and the underlying mechanism may be down regulating the activities and expressions of ATP-binding cassette transporters and GSTs

A comparative analysis of morphology, microstructure, and volatile metabolomics of leaves at varied developmental stages in Ainaxiang (Blumea balsamifera (Linn.) DC.)

IntroductionAinaxiang (Blumea balsamifera (Linn.) DC.) is cultivated for the extraction of (-)-borneol and other pharmaceutical raw materials due to its abundant volatile oil. However, there is limited knowledge regarding the structural basis and composition of volatile oil accumulation in fresh B. balsamifera leaves.MethodsTo address this problem, we compare the fresh leaves’ morphology, microstructure, and volatile metabonomic at different development stages, orderly defined from the recently unfolded young stage (S1) to the senescent stage (S4).Results and discussionDistinct differences were observed in the macro-appearance and microstructure at each stage, particularly in the B. balsamifera glandular trichomes (BbGTs) distribution. This specialized structure may be responsible for the accumulation of volatile matter. 213 metabolites were identified through metabolomic analysis, which exhibited spatiotemporal accumulation patterns among different stages. Notably, (-)-borneol was enriched at S1, while 10 key odor metabolites associated with the characteristic balsamic, borneol, fresh, and camphor aromas of B. balsamifera were enriched in S1 and S2. Ultra-microstructural examination revealed the involvement of chloroplasts, mitochondria, endoplasmic reticulum, and vacuoles in the synthesizing, transporting, and storing essential oils. These findings confirm that BbGTs serve as the secretory structures in B. balsamifera, with the population and morphology of BbGTs potentially serving as biomarkers for (-)-borneol accumulation. Overall, young B. balsamifera leaves with dense BbGTs represent a rich (-)-borneol source, while mesophyll cells contribute to volatile oil accumulation. These findings reveal the essential oil accumulation characteristics in B. balsamifera, providing a foundation for further understanding

Assembly of 500,000 inter-specific catfish expressed sequence tags and large scale gene-associated marker development for whole genome association studies

Twelve cDNA libraries from two species of catfish have been sequenced, resulting in the generation of nearly 500,000 ESTs