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  • 1
    Electronic Resource
    Electronic Resource
    Using a recirculating seawatef system for the maintenance of young mullets (Teleostei, Mugilidae) in a laboratory
    Amsterdam : Elsevier
    Aquaculture 7 (1976), S. 347-355 
    Details
    ISSN: 0044-8486
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1016/0044-8486(76)90131-9
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    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Modulation of fatty acid-binding protein content of adult rat heart in response to chronic changes in plasma lipid levels (1993)
    Springer
    Molecular and cellular biochemistry 123 (1993), S. 107-112 
    Details
    ISSN: 1573-4919
    Keywords: fatty acid-binding protein ; lipid metabolism ; Clofibrate ; intralipid ; chronic hypoxia ; rat heart
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The aim of this work was to study in the adult rat heart the effect of modifications of fatty acid (FA) supply on the content of cytoplasmic fatty acid-binding protein (H-FABPc). To modify the amount of circulating lipids, three different treatments were chosen: (i) an hypolipidemic treatment with Clofibrate, administered daily through a gastric tube at a dose of 250 mg/kg per day for one week, (ii) a continuous intravenous infusion of 20% Intralipid, a fat emulsion, for one week at a dose of 96 ml/kg per day, and (iii) a normobaric hypoxia exposure (pO2=10%) for three weeks. At the end of each treatment plasma lipids, myocardial H-FABPc content and the activities of three key enzymes (citrate synthase, CS, fructrose-6-phosphate kinase, FPK and hydroxy-acyl CoA-dehydrogenase, HAD) were assessed. With each of the three treatments a decrease of plasma cholesterol and phospholipid levels was observed. Plasma FA concentration increased with Intralipid infusion and decreased with chronic hypoxia. The heart H-FABPc content was increased by 20% with Clofibrate, decreased by 20% with chronic hypoxia and remained unaltered upon Intralipid treatment. The induced changes in H-FABPc content were not related directly to changes in plasma lipid levels. CS activity was slightly decreased in the hypoxia group, FPK activity decreased in the Clofibrate group, and HAD activity decreased in the Intralipid group. Among the various groups heart H-FABPc content was related to HAD activity. In conclusion, the H-FABPc content of adult rat heart appears responsive to changes in plasma lipid levels.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01076481
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Is oxygen supply sufficient to induce normoxic conditions in isolated rat heart? (1994)
    Springer
    Basic research in cardiology 89 (1994), S. 535-544 
    Details
    ISSN: 1435-1803
    Keywords: isolated rat heart ; graded hypoxia ; heart function ; oxygen uptake ; glycolytic ATP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The aim of this study is to assess whether oxygen supply is sufficient to induce normoxic conditions in isolated rat hearts. Hearts are perfused with a Krebs medium supplemented with 11mM glucose, 0.6 mM lactate, 0.06 mM pyruvate, non delipidated albumin (0.1 mM fatty acids), and either 1.78 mM or 0.76 mM free calcium, at 10ml.min−1. Graded hypoxia is induced by a stepwise decrease of partial pressure of oxygen (PO2) from 660 to 52 mmHg. Contractile performance, oxygen uptake and lactate plus pyruvate balance are assessed. With high calcium, left ventricular developed pressure, dP/dt max and oxygen uptake increase linearly with PO2 up to 660 mmHg; heart rate increases with PO2 up to 250 mmHg and then tends to stabilize. With low calcium, all parameters reach a plateau over 400 mmHg. Lactate plus pyruvate production suggests a stimulation of glycolysis with high calcium, even at 660 mmHg; conversely, there is no lactate plus pyruvate production with low calcium over 250 mmHg. In conclusion, our results demonstrate that, under a high level of calcium at a constant flow of 10 ml.min−1, cardiac function is always limited by O2 supply, except for heart rate. This raises the question as to the definition of a normoxic state. The better preservation of heart rate during hypoxia, compared to other dynamic parameters, could be explained by a contribution of glycolytic ATP.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00794953
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    Paper (German National Licenses)
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  • 4
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    Nuclear CaMKII Signaling in Cardiac Progenitor Cells [Gene Regulation] (2015)
    The American Society for Biochemistry and Molecular Biology (ASBMB)
    Details
    Publication Date: 2015-10-17
    Description: Ca2+/Calmodulin-dependent protein kinase II (CaMKII) signaling in the heart regulates cardiomyocyte contractility and growth in response to elevated intracellular Ca2+. The δB isoform of CaMKII is the predominant nuclear splice variant in the adult heart and regulates cardiomyocyte hypertrophic gene expression by signaling to the histone deacetylase HDAC4. However, the role of CaMKIIδ in cardiac progenitor cells (CPCs) has not been previously explored. During post-natal growth endogenous CPCs display primarily cytosolic CaMKIIδ, which localizes to the nuclear compartment of CPCs after myocardial infarction injury. CPCs undergoing early differentiation in vitro increase levels of CaMKIIδB in the nuclear compartment where the kinase may contribute to the regulation of CPC commitment. CPCs modified with lentiviral-based constructs to overexpress CaMKIIδB (CPCeδB) have reduced proliferative rate compared with CPCs expressing eGFP alone (CPCe). Additionally, stable expression of CaMKIIδB promotes distinct morphological changes such as increased cell surface area and length of cells compared with CPCe. CPCeδB are resistant to oxidative stress induced by hydrogen peroxide (H2O2) relative to CPCe, whereas knockdown of CaMKIIδB resulted in an up-regulation of cell death and cellular senescence markers compared with scrambled treated controls. Dexamethasone (Dex) treatment increased mRNA and protein expression of cardiomyogenic markers cardiac troponin T and α-smooth muscle actin in CPCeδB compared with CPCe, suggesting increased differentiation. Therefore, CaMKIIδB may serve as a novel modulatory protein to enhance CPC survival and commitment into the cardiac and smooth muscle lineages.
    Print ISSN: 0021-9258
    Electronic ISSN: 1083-351X
    Topics: Biology , Chemistry and Pharmacology
    Published by The American Society for Biochemistry and Molecular Biology (ASBMB)
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  • 5
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    Nuclear CaMKII enhances histone H3 phosphorylation and remodels chromatin during cardiac hypertrophy (2013)
    Oxford University Press
    Details
    Publication Date: 2013-09-06
    Description: Calcium/calmodulin-dependent protein kinase II (CaMKII) plays a central role in pathological cardiac hypertrophy, but the mechanisms by which it modulates gene activity in the nucleus to mediate hypertrophic signaling remain unclear. Here, we report that nuclear CaMKII activates cardiac transcription by directly binding to chromatin and regulating the phosphorylation of histone H3 at serine-10. These specific activities are demonstrated both in vitro and in primary neonatal rat cardiomyocytes. Activation of CaMKII signaling by hypertrophic agonists increases H3 phosphorylation in primary cardiac cells and is accompanied by concomitant cellular hypertrophy. Conversely, specific silencing of nuclear CaMKII using RNA interference reduces both H3 phosphorylation and cellular hypertrophy. The hyper-phosphorylation of H3 associated with increased chromatin binding of CaMKII occurs at specific gene loci reactivated during cardiac hypertrophy. Importantly, H3 Ser-10 phosphorylation and CaMKII recruitment are associated with increased chromatin accessibility and are required for chromatin-mediated transcription of the Mef2 transcription factor. Unlike phosphorylation of H3 by other kinases, which regulates cellular proliferation and immediate early gene activation, CaMKII-mediated signaling to H3 is associated with hypertrophic growth. These observations reveal a previously unrecognized function of CaMKII as a kinase signaling to histone H3 and remodeling chromatin. They suggest a new epigenetic mechanism controlling cardiac hypertrophy.
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
    Published by Oxford University Press
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  • 6
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    Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis (2013)
    Oxford University Press
    Details
    Publication Date: 2013-05-14
    Description: Primary microcephaly (PM) is a developmental disorder of early neuroprogenitors that results in reduction of the brain mass, particularly the cortex. To gain fresh insight into the pathogenesis of PM, we describe a consanguineous family with a novel genetic variant responsible for the disease. We performed autozygosity mapping followed by exome sequencing to detect the causal genetic variant. Several functional assays in cells expressing the wild-type or mutant gene were performed to understand the pathogenesis of the identified mutation. We identify a novel mutation in PHC1 , a human orthologue of the Drosophila polyhomeotic member of polycomb group (PcG), which significantly decreases PHC1 protein expression, increases Geminin protein level and markedly abolishes the capacity to ubiquitinate histone H2A in patient cells. PHC1 depletion in control cells similarly enhances Geminin expression and decreases histone H2A ubiquitination. The ubiquitination defect and accumulation of Geminin with consequent defect in cell cycle are rescued by over-expression of PHC1 in patient cells. Although patients with the PHC1 mutation exhibit PM with no overt progression of the disease, patient cells also show aberrant DNA damage repair, which is rescued by PHC1 overexpression. These findings reveal several cellular defects in cells carrying the PHC1 mutation and highlight the role of chromatin remodeling in the pathogenesis of PM.
    Print ISSN: 0964-6906
    Electronic ISSN: 1460-2083
    Topics: Biology , Medicine
    Published by Oxford University Press
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