21 research outputs found

    CATALYST - Architecture as a catalyst for social and socio-economic value creation

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    Ecosystem service benefits and trade-offs-selecting tree species in Denmark for bioenergy production

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    Research highlights: The study enabled us to quantitatively assess ecosystem benefits and trade-offs, to characterize species as generalists or specialists, and findings suggest that producing biomass for energy is more likely to serve multiple objectives if it is implemented in an integrated production system. Background and Objectives: Biomass is one of the main and largest sources of renewable energy. In Denmark, the production of biomass for energy is mainly based on timber harvest residues from pre-commercial thinning of forest stands. However, there is an increasing demand for bioenergy that require biomass to be grown specifically for energy purposes even though the sustainability and climate change mitigation potential of bioenergy plantations have recently been questioned in terms of food production, land use, land use change and terrestrial carbon cycles. The overall objective of the research is to better understand the opportunities and trade-offs between different woody and non-woody energy crops. Material and Methods: This study assessed the ecosystem services of seven woody species and one perennial along a management intensity continuum with a main focus on bioenergy production. Results: Results of the analysis showed that there are complex interrelations between ecosystem services and significant differences between species in providing those services. Conclusions: Species with a highest energy benefit among assessed species were poplar and grand fir, while beech and oak proved the best in providing biodiversity benefits

    Proteomic Analysis of Cerebrospinal Fluid in Alzheimer's Disease: Wanted Dead or Alive.

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    Clinical diagnosis of Alzheimer's disease (AD) relying on symptomatic features has a low specificity, emphasizing the importance of the pragmatic use of neurochemical biomarkers. The most advanced and reliable markers are amyloid-beta (Abeta42), total tau (t-tau), and phosphorylated tau (p-tau) in cerebrospinal fluid (CSF) with relatively high levels of sensitivity, specificity, and diagnostic accuracy. Recent advances within the field of proteomics offer the potential to search for novel biomarkers in CSF by using modern methods, such as microarrays. The purpose of this study was to identify pathognostic proteins in CSF obtained from patients whose clinical AD diagnosis was confirmed by the "core" biomarkers. CSF samples were obtained from 25 AD patients and 25 control individuals. The levels of Abeta42, t-tau, and p-tau were measured by ELISA. In the microarray experiments, ultrasensitive slides representing of 653 antigens were used. Apolipoprotein E genotyping was also determined. A decrease of seven CSF proteins in AD were found, four of them (POLG, MGMT, parkin, and ApoD) have a protective function against neuronal death, while the remaining three proteins (PAR-4, granzyme B, Cdk5) trigger multiple pathways facilitating neuronal cell death. Since these proteins from CSF samples could not be identified by western blot, their decreased levels in AD patients were not verified. Our results provide new information of pathognostic importance of POLG and granzyme B in AD. Although the function of MGMT, parkin, ApoD, PAR-4, and Cdk5 was previously known in AD, the findings presented here provide novel evidence of the significance of CSF analysis in the mapping of the AD pathomechanism

    Cytoskeletal protein translation and expression in the rat brain are stressor-dependent and region-specific.

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    Stress is an integral component of life that can sometimes cause a critical overload, depending on the qualitative and quantitative natures of the stressors. The involvement of actin, the predominant component of dendritic integrity, is a plausible candidate factor in stress-induced neuronal cytoskeletal changes. The major aim of this study was to compare the effects of three different stress conditions on the transcription and translation of actin-related cytoskeletal genes in the rat brain. Male Wistar rats were exposed to one or other of the frequently used models of physical stress, i.e. electric foot shock stress (EFSS), forced swimming stress (FSS), or psychosocial stress (PSS) for periods of 3, 7, 14, or 21 days. The relative mRNA and protein expressions of β-actin, cofilin and mitogen-activated protein kinase 1 (MAPK-1) were determined by qRT- PCR and western blotting from hippocampus and frontal cortex samples. Stressor-specific alterations in both β-actin and cofilin expression levels were seen after stress. These alterations were most pronounced in response to EFSS, and exhibited a U-shaped time course. FSS led to a significant β-actin mRNA expression elevation in the hippocampus and the frontal cortex after 3 and 7 days, respectively, without any subsequent change. PSS did not cause any change in β-actin or cofilin mRNA or protein expression in the examined brain regions. EFSS, FSS and PSS had no effect on the expression of MAPK-1 mRNA at any tested time point. These findings indicate a very delicate, stress type-dependent regulation of neuronal cytoskeletal components in the rat hippocampus and frontal cortex
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