17 research outputs found

    Visceral adipose tissue but not subcutaneous adipose tissue is associated with urine and serum metabolites

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    Obesity is a complex multifactorial phenotype that influences several metabolic pathways. Yet, few studies have examined the relations of different body fat compartments to urinary and serum metabolites. Anthropometric phenotypes (visceral adipose tissue (VAT), subcutaneous adipose tissue (SAT), the ratio between VAT and SAT (VSR), body mass index (BMI), waist circumference (WC)) and urinary and serum metabolite concentrations measured by nuclear magnetic resonance spectroscopy were measured in a population-based sample of 228 healthy adults. Multivariable linear and logistic regression models, corrected for multiple testing using the false discovery rate, were used to associate anthropometric phenotypes with metabolites. We adjusted for potential confounding variables: age, sex, smoking, physical activity, menopausal status, estimated glomerular filtration rate (eGFR), urinary glucose, and fasting status. In a fully adjusted logistic regression model dichotomized for the absence or presence of quantifiable metabolite amounts, VAT, BMI and WC were inversely related to urinary choline (ß = -0.18, p = 2.73*10−3), glycolic acid (ß = -0.20, 0.02), and guanidinoacetic acid (ß = -0.12, p = 0.04), and positively related to ethanolamine (ß = 0.18, p = 0.02) and dimethylamine (ß = 0.32, p = 0.02). BMI and WC were additionally inversely related to urinary glutamine and lactic acid. Moreover, WC was inversely associated with the detection of serine. VAT, but none of the other anthropometric parameters, was related to serum essential amino acids, such as valine, isoleucine, and phenylalanine among men. Compared to other adiposity measures, VAT demonstrated the strongest and most significant relations to urinary and serum metabolites. The distinct relations of VAT, SAT, VSR, BMI, and WC to metabolites emphasize the importance of accurately differentiating between body fat compartments when evaluating the potential role of metabolic regulation in the development of obesity-related diseases, such as insulin resistance, type 2 diabetes, and cardiovascular disease

    Sustainable and resource efficient intensivation of crop production – Perspectives of agro-ecosystem researchPolicy paper of the DFG Senate Commission on Agroecosystem Research

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    Mit dem vorliegenden Grundsatzpapier zeigt die Senatskommission für Agrarökosystemforschung Perspektiven für die Grundlagenforschung zur nachhaltigen Erhöhung der Kulturpflanzenproduktion auf.Agrarsysteme stehen im Spannungsfeld zwischen steigendem Bedarf an landwirtschaftlichen Produkten, der Verknappung der Ressourcen, dem Verlust der Biodiversität und dem Klimawandel. Die für das Jahr 2050 prognostizierte notwendige Ertragssteigerung zur Sicherstellung des Bedarfs an Nahrungsmitteln kann, ohne die Belastbarkeitsgrenzen ökologischer Systeme zu überschreiten, nur durch wissenschaftlichen Fortschritt bewältigt werden (Abb. 1), der eine nachhaltige und ressourcen­effiziente Steigerung der Agrarproduktion ermöglicht (FAO, 2011; Dobermann und Nelson, 2013). Die nachhaltige Intensivierung stellt die Agrarwissenschaften vor neue Aufgaben, die weit über ihre klassischen Grenzen hinausgehen.Die Senatskommission plädiert daher für eine Erweiterung der agrarwissenschaftlichen Perspektive. Die meist auf einzelne Feldfrüchte bezogene Bewertung der Rela­tion zwischen Input und Ertrag muss ergänzt werden um die Optionen, die sich aus der räumlichen und zeitlichen Diversifikation der Produktionssysteme unter Einbeziehung der standörtlichen Eigenschaften, des Landschaftskontextes sowie des Klimawandels ergeben. Um Ökosystemleistungen einzubeziehen, müssen Produktionsstrategien entwickelt werden, die sich auf ganze Landschaften und Regionen richten und auch entsprechende sozio­öko­no­mische und agrarpolitische Rahmenbedingungen berücksichtigen.Vor diesem Hintergrund schlägt die Senatskommission drei interdisziplinäre Forschungsschwerpunkte zur ressourceneffizienten Erhöhung der Flächenproduktivität vor:(1) Ausnutzung des Potentials von Kulturpflanzen zur umweltschonenden Ertragssteigerung im Kontext öko­systemarer Bedingungen.(2) Nachhaltige Steigerung der Pflanzenproduktion im Landschaftskontext.(3) Ökonomische, gesellschaftliche und politische Dimensionen der Ertragssteigerung von Kulturpflanzen. DOI: 10.5073/JfK.2014.07.01, https://doi.org/10.5073/JfK.2014.07.01With its policy paper the Senate Commission on Agro-ecosystem Research of the Deutsche Forschungsgemeinschaft (DFG) summarizes potential benefits of basic research for the sustainable intensification of crop production. Agro-ecosystems critically contribute to fulfilling the need for increasing food and fiber production, diminishing resource depletion as well as counteracting biodiversity loss and climate change. Yield demands that are needed to ensure the food supply predicted for the year 2050 can only be achieved by scientific progress that allows the intensive yet environmentally friendly production of plant biomass (Figure 1), (FAO, 2011; Dobermann und Nelson, 2013; Ray et al., 2013). Sustainable intensification requires a scientific realignment that allows for broadening the scope of agricultural research. The productivity of farming systems should be evaluated with regard to their efficiency (input-output relation). In addition, the spatial and temporal variability of these systems must be considered by addressing local conditions, the landscape context and climate change. With respect to ecosystem services, new production strategies must be developed that take all aspects of landscape and regional complexity as well as socio-economic conditions and agricultural policy into account.Against this background, the Senate Commission on Agro-ecosystem Research proposes three priority areas of interdisciplinary research on resource efficient intensification of crop production:(1) Exploiting the biological potential of the individual crop plants for an environmentally friendly intensification in an ecosystem approach(2) Exploring sustainable intensification of crop production within a landscape context(3) Taking full account of the economic, social and political dimensions of sustainable intensification of crop production DOI: 10.5073/JfK.2014.07.01, https://doi.org/10.5073/JfK.2014.07.0

    Bibel und Babel : eine Darstellung für Schüler

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    von Johannes SchlechtProgr.-Nr. 20

    Two-dimensional capillary electrophoresis-mass spectrometry (CE-CE-MS): coupling MS-interfering capillary electromigration methods with mass spectrometry

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    Electromigration separation techniques often demand certain compounds in the electrolyte to achieve the required selectivity and efficiency. These compounds, including the electrolyte itself, ampholytes, polymeric compounds for sieving, complexing agents, tensides, etc. are often non-volatile. Thus, interference with the electrospray ionization process is a common issue, impeding direct coupling of such electrolyte systems to mass spectrometry. Still, several options exist to obtain mass spectra after separation, including offline fractionation, alternative ionization, dilution, or the change to volatile constituents. In the first part of this article, these methods are discussed. However, all of these options are a compromise of separation performance and sensitivity of mass spectrometric detection. Two-dimensional capillary electrophoresis-mass spectrometry (CE-CE-MS) systems represent a promising alternative to the aforementioned challenges, as they allow the use of existing methods with best separation performance in combination with sensitive mass characterization. In this context, the second part of this article is dedicated to the advantages, limitations, and applications of this approach. Finally, an outlook towards future developments is given

    Oeconomiæ Corporis Humani Brevis Descriptio Continuata

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    OECONOMIÆ CORPORIS HUMANI BREVIS DESCRIPTIO CONTINUATA Oeconomiæ Corporis Humani Brevis Descriptio Continuata ([1]) Einband ( - ) Titelseite ([1]) Text (3

    Online mass spectrometry of CE (SDS)-separated proteins by two-dimensional capillary electrophoresis

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    Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) is the fundamental technique for protein separation by size. Applying this technology in capillary format, gaining high separation efficiency in a more automated way, is a key technology for size separation of proteins in the biopharmaceutical industry. However, unequivocal identification by online mass spectrometry (MS) is impossible so far, due to strong interference in the electrospray process by SDS and other components of the SDS-MW separation gel buffer. Here, a heart-cut two-dimensional electrophoretic separation system applying an electrically isolated valve with an internal loop of 20 nL is presented. The peak of interest in the CE (SDS) separation is transferred to the CZE-MS, where electrospray-interfering substances of the SDS-MW gel are separated prior to online electrospray ionization mass spectrometry. An online SDS removal strategy for decomplexing the protein-SDS complex is implemented in the second dimension, consisting of the co-injection of organic solvent and cationic surfactant. This online CE (SDS)-CZE-MS system allows MS characterization of proteoforms separated in generic CE (SDS), gaining additional separation in the CZE and detailed MS information. In general, the system can be applied to all kinds of proteins separated by CE (SDS). Here, we present results of the CE (SDS)-CZE-MS system on the analysis of several biopharmaceutically relevant antibody impurities and fragments. Additionally, the versatile application spectrum of the system is demonstrated by the analysis of extracted proteins from soybean flour. The online hyphenation of CE (SDS) resolving power and MS identification capabilities will be a powerful tool for protein and mAb characterization. Graphical abstract Two-dimensional capillary electrophoresis system hyphenated with mass spectrometry for the characterization of CE (SDS)-separated proteins. As first dimension, a generic and high MS-interfering CE (SDS) separation is performed for size separation. After heart-cut transfer of the unknown CE (SDS) protein peak, via a four-port nanoliter valve to a volatile electrolyte system as second dimension, interference-free mass spectrometric data of separated mAb fragments and soybean proteins are obtained
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