Changes in the lungs in the early period of closed trauma of the thorax in rats

In experiments on rats it has been demonstrated that in the acute period of uninjured parts of the lungs periodic changes of protein, lipid and glucose concentrations developed. In uninjured parts of the lungs one can observe more concentration of lipids and in injured parts-more glucose. The changes of substrates, concentrations in the lungs are due to not only the changes of venous blood excess in the lungs, but are connected with metabolic changes in the cells of the injured and uninjured parts of the lungs. The metabolic changes in the lungs in the acute period of chest trauma influence the creation of such indices of gas exchange as PaCO2 and PACO2.     

Long non‐coding RNAs in melanoma

Melanoma is the most lethal cutaneous cancer with a highly aggressive and metastatic phenotype. While recent genetic and epigenetic studies have shed new insights into the mechanism of melanoma development, the involvement of regulatory non‐coding RNAs remain unclear. Long non‐coding RNAs (lncRNAs) are a group of endogenous non‐protein‐coding RNAs with the capacity to regulate gene expression at multiple levels. Recent evidences have shown that lncRNAs can regulate many cellular processes, such as cell proliferation, differentiation, migration and invasion. In the melanoma, deregulation of a number of lncRNAs, such as HOTAIR, MALAT1, BANCR, ANRIL, SPRY‐IT1 and SAMMSON, have been reported. Our review summarizes the functional role of lncRNAs in melanoma and their potential clinical application for diagnosis, prognostication and treatment.     

Protective effect of bixin on carbon tetrachloride-induced hepatotoxicity in rats

Background

The liver is an important organ for its ability to transform xenobiotics, making the liver tissue a prime target for toxic substances. The carotenoid bixin present in annatto is an antioxidant that can protect cells and tissues against the deleterious effects of free radicals. In this study, we evaluated the protective effect of bixin on liver damage induced by carbon tetrachloride (CCl₄) in rats.

Results

The animals were divided into four groups with six rats in each group. CCl₄ (0.125 mL kg^-1 body wt.) was injected intraperitoneally, and bixin (5.0 mg kg^-1 body wt.) was given by gavage 7 days before the CCl₄ injection. Bixin prevented the liver damage caused by CCl₄, as noted by the significant decrease in serum aminotransferases release. Bixin protected the liver against the oxidizing effects of CCl₄ by preventing a decrease in glutathione reductase activity and the levels of reduced glutathione and NADPH. The peroxidation of membrane lipids and histopathological damage of the liver was significantly prevented by bixin treatment.

Conclusion

Therefore, we can conclude that the protective effect of bixin against hepatotoxicity induced by CCl₄ is related to the antioxidant activity of the compound.     

Metabolism of Yarrowia lipolytica grown on ethanol under conditions promoting the production of alpha-ketoglutaric and citric acids: a comparative study of the central metabolism enzymes

A comparative study of the enzymes of the tricarboxylic acid (TCA) and glyoxylate cycles in the mutant Yarrowia lipolytica strain N1 capable of producing alpha-ketoglutaric acid (KGA) and citric acid showed that almost all enzymes of the TCA cycle are more active under conditions promoting the production of KGA. The only exception was citrate synthase, whose activity was higher in yeast cells producing citric acid. The production of both acids was accompanied by suppression of the glyoxylate cycle enzymes. The activities of malate dehydrogenase, aconitase, NADP-dependent isocitrate dehydrogenase, and fumarase were higher in cells producing KGA than in cells producing citric acid.     

Oligochaete communities at the mouth of the Neva and their relationship to anthropogenic impact

Changes in the oligochaete community of the Neva Mouth for the period 1982–1993 are discussed in relation to anthropogenic impacts. A number of community parameters such as species composition, biomass and diversity were generally stable, although local changes were noted. Predominance of eutrophic species, i.e. L. hoffmeisteri, T. tubifex, P. hammoniensis was enhanced, whereas mesotrophic and oligotrophic species — L. isoporus, S. heringianus, T. newaensis disappeared or became less numerous at some stations. The reverse trend was observed at other stations. These phenomena were accompanied by a sharp increase in the variability of biomass and/or diversity, which is regarded as exceeding normal annual fluctuations. The oligochaete community is recognized as a promising indicator of the ecological situation in the Neva Mouth.     

Characterization model to assess ocean acidification within life cycle assessment

Purpose

Ocean acidification due to the absorption of increasing amounts of atmospheric carbon dioxide has become a severe problem in the recent years as more and more marine species are influenced by the decreasing pH value as well as by the reduced carbonate ion concentration. So far, no characterization model exists for ocean acidification. This paper aims to establish such a characterization model to allow for the necessary future inclusion of ocean acidification in life cycle assessment (LCA) case studies.

Methods

Based on a cause-effect chain for ocean acidification, the substances carbon monoxide, carbon dioxide, and methane were identified as relevant for this impact category. In a next step, the fate factor representing the substances’ share absorbed by the ocean due to conversion, distribution, and dissolution is determined. Then, the fate sensitivity factor is established reflecting the changes in the marine environment due to the amount of released hydrogen ions per gram of substance (category indicator). Finally, fate and fate sensitivity factors of each substance are multiplied and set in relation to the reference substance, carbon dioxide, thereby delivering the respective characterization factors (in kg CO₂ eq) at midpoint level.

Results and discussion

Characterization factors are provided for carbon monoxide (0.87 kg CO₂ eq), carbon dioxide (1 kg CO₂ eq), and methane (0.84 kg CO₂ eq), which allow conversion of inventory results of these substances into category indicator results for ocean acidification. Inventory data of these substances is available in common LCA databases and software. Hence, the developed method is directly applicable. In a subsequent contribution analysis, the relative contribution of the three selected substances, along with other known acidifying substances, to the ocean acidification potential of 100 different materials was studied. The contribution analysis confirmed carbon dioxide as the predominant substance responsible for more than 97 % of the total ocean acidification potential. However, the influence of other acidifying substances, e.g., sulfur dioxide, should not be neglected.

Conclusions

Evaluation of substances contributing to ocean acidification is of growing importance since the acidity of oceans has been increasing steadily over the last decades. The introduced approach can be applied to evaluate product system related impacts of ocean acidification and include those into current LCA practice.

     

Effect of emulsifiers released by yeasts multiplying on n-alkane media on their growth and microscopic organization

Bioemulsifiers and ether extracts from the cultural broth of yeast cells were used to study their effect of Candida lipolytica growth and ultrastructural organisation. When the emulsifiers and ether extracts were added to the growth medium, the lag phase was reduced but the growth rate did not change. The ether extracts increased the growth rate of C. lipolytica 374/2 and the final biomass yield of C. lipolytica 704. The ultrastructural organisation of C. lipolytica 374/2 cells changed under the action of the bioemulsifier added to the growth medium.     

Induction of cytochrome P-450 and ethanol oxidation in Yarrowia lipolytica

The study of the effect of different ethanol concentrations in the medium on the growth and the activity of enzymatic systems involved in ethanol oxidation in Yarrowia lipolytica showed that the cultivation of yeast cells on 1 and 2% ethanol caused their rapid growth and a drastic increase in cell respiration and sensitivity to cyanide already in the first hours of cultivation. At the same time, during cultivation on 3, 4, and 5% ethanol, the growth and respiration of yeast cells were considerably suppressed. All of the ethanol concentrations studied induced the synthesis of cytochrome P-450, its dynamics in cells being dependent on the initial concentration of ethanol in the medium. When the initial concentration of ethanol was 1 and 2%, the content of cytochrome P-450 in cells steeply decreased after a short period of induction. But when the initial concentration of ethanol in the medium was 3 to 5%, the content of cytochrome P-450 in cells was high throughout the cultivation period. The induction of cytochrome P-450 in cells preceded the induction of the NAD-dependent enzymes alcohol dehydrogenase and catalase, which, like cytochrome P-450, are also involved in ethanol oxidation by yeasts. The activity of catalase was higher in the yeast cells grown in the presence of 3 to 5% ethanol than in the cells grown in the presence of 1 and 2% ethanol. The roles played by cytochrome P-450, alcohol dehydrogenase, and catalase in ethanol oxidation by yeast cells are discussed.     

Organic Acid Production by the Yeast <Emphasis Type="Italic">Yarrowia lipolytica</Emphasis>: A Review of Prospects

The review sums up the results of studies of (1) physiological growth characteristics of the yeast Yarrowia lipolytica cultured in the presence of diverse carbon sources (n-alkanes, glucose, and glycerol) and (2) superhigh synthesis of organic acids, which was performed at the Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences. Microbiological processes of obtaining α-ketoglutaric, pyruvic, isocitric, and citric acids are discussed.