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  • 11
    ISSN: 1432-2013
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Zusammenfassung Die physikalisch-elektronischen Eigenschaften von Strömungswandlern zur induktiven Messung der Blutströmungsgeschwindigkeit an uneröffneten Gefäßen werden analysiert. Ein Verfahren zur Herstellung verbesserter Strömungswandler wird beschrieben. Die entwickelten Instrumente unterscheiden sich von den in der Literatur beschriebenen und im Handel erhältlichen Typen durch folgende Vorteile: 1. Starke Reduzierung der induktiven Störspannung bis auf höchstens etwa 10–20% des zu erwartenden Nutzsignals. 2. Völlige Unterdrückung des kapazitiven Störsignals. 3. Unterdrückung von Verlustwiderständen, verursacht durch Feuchtigkeitsaufnahme bei chronischer Implantation. Diese Verbesserungen konnten erreicht werden durch folgende Abweichungen vom Kolinschen3 Vorgehen: 1. Die fast völlige Eliminierung der induktiven Störspannung ist nur möglich durch Anpassung der Spulenposition gegenüber der Lage der Elektrodenzuleitung und nicht umgekehrt, vorausgesetzt, daß es sich um magnetkernlose Strömungswandler handelt. 2. Eine durch galvanische Metallisierung gewonnene Zwischenschicht zwischen Elektrodenebene und Spulenebene erwies sich als ein guter statischer Schirm, welcher kapazitives „Übersprechen“ von den Spulen auf die Elektroden verhindert. 3. Der Metallschirm erwies sich gleichzeitig als eine Sperre gegen die Feuchtigkeitsaufnahme bei chronischer Implantation des Strömungswandlers. 4. Die Kombination von Polycarbonaten, Silikonkautschuk und Akrylaten (als Verbindungsmittel) erwies sich bei der Konstruktion von Strömungswandlern als besonders günstig. 5. Mit wenigen Lagen dünnen Eisendrahtes lassen sich besonders kleindimensionierte Magneten für kleine Blutgefäße herstellen.
    Type of Medium: Electronic Resource
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  • 12
    ISSN: 1573-4919
    Keywords: hibernating myocardium ; repair mechanism ; functional recovery ; TGF-β1
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Recently, we proposed the hypothesis that a vicious cycle exists in human hibernating myocardium (HM) between the progression of myocyte degeneration and the development of fibrosis [1]. We now investigated the pathomechanism of this cycle in more detail and established a correlation between the severity of the morphological changes and the degree of postoperative functional recovery of HM. HM was diagnosed by dobutamine echocardiography, thallium-201 scintigraphy and radionuclide ventriculography. Functional recovery was present at 3 months after coronary bypass surgery but remained unchanged at 15 months. Forty patients were subdivided into 2 groups: A with complete and B with incomplete recovery. Biopsies taken during surgery and studied by electron microscopy, immunocytochemistry, rt-PCR, and morphometry revealed myocyte degeneration and inflammatory and fibrinogenic changes in a widened interstitial space. We report here for the first time an upregulation of TGF-β1 evident by a 5-fold increase of fibroblasts and macrophages exhibiting a TGF-β1 content 3-fold larger than in control, and a 〉 3-fold increase in TGF-β1 mRNA by rt-PCR. The number of angiotensin converting enzyme (ACE) containing structures was increased (n/mm2: control - 11.4, A - 17.6, B - 19.2, control vs. A and B, p 〈 0.05). Fibrosis was more severe in group B than A or control (%: C - 10.1; A - 21.2; B - 40.6; p 〈 0.05). Capillary density was significantly reduced (n/mm2: C - 1152; A - 782; B - 579, p 〈 0.05) and intercapillary distance was widened (μm: C - 29.5, A - 36.1, B - 43.3, p 〈 0.05). The number of CD 3 (n/mm2: C - 5.0; A - 9.6; B - 9.4, ns) and CD 68 positive cells (n/mm2: C - 37.2; A - 80.7; B - 55.0, C vs. A p 〈 0.05) was elevated in HM as compared to control indicating an inflammatory reaction. Cut-off points for functional recovery are fibrosis 〉 32%, capillary density 〈 660/mm2 and intercapillary distance 〉 39.0 μm. In HM a self-perpetuating vicious cycle of tissue alterations leads to progressive replacement fibrosis and continuous intracellular degeneration which should be interrupted by early revascularization.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Molecular and cellular biochemistry 160-161 (1996), S. 209-215 
    ISSN: 1573-4919
    Keywords: myocardial ischemia ; stunned myocardium ; preconditioning ; angiogenic response
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Helmholtz is quoted to have said that if he'd had any influence in creation he would have returned the human eye to its maker for revisions. The same could be said of the heart with its only very rudimentary ability to defend itself against ischemia. Ischemia was obviously not a problem during evolution: Early man did not live much longer than prime time for reproduction and no selection bias existed to prevent vascular diseases, an affliction of later life. In spite of this natural disadvantage of aged males the number of existing although not very efficient defense mechanisms is surprisingly large. It is the general belief that the knowledge of these mechanisms may lead to the development of new therapies that hopefully improve the imperfect product of natural selection. (Mol Cell Biochem 160/161: 209–215, 1996)
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Molecular and cellular biochemistry 186 (1998), S. 43-51 
    ISSN: 1573-4919
    Keywords: myocardial ischemia ; gene expression ; growth factors ; phospholamban ; calsequestrin heat shock proteins ; preconditioning ; stunning
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Brief periods of coronary occlusion render the affected myocardium more tolarant to the otherwise devastating effects of long coronary occlusion. Besides this phenomena, called ischemic preconditioning, short periods of ischemia cause a regional dysfunction, namely myocardial stunning. The molecular mechanisms of both syndromes are not very well understood. We therefore investigated the expression of genes which may be involved in cardioprotection or repair processes.Using our porcine model of ischemia and reperfusion we were able to show an induction of genes coding for transcription factors (proto-oncogenes), for proteins involved in repair processes (heat shock genes), for proteins implicated in the calcium homeostasis (calcium-handling genes) and for growth factors. We could show that the increased mRNA levels are due to an enhanced transcriptional activity and not to a prolonged half-life of the transcripts. The angiogenic growth factor vascular endothelial growth factor (VEGF) represents an exception. It exhibits - in addition to a HIF-motif (Hypoxia Inducible Factor) in its promoter/enhancer - a protein binding region in its 3′ UTR which when occupied renders the mRNA more stable. However to what extent the expression of the distinct genes contributes to the cardioprotective effect of ischemic preconditioning or myocardial stunning can only be presumed. Increased mRNA stability can be confered via adenosine which is produced during ischemia by ATP-breakdown. The demasking of unknown genes - via differential display reverse transcription polymerase chain reaction (DDRT-PCR) - should provide a more comprehensive view of the mechanisms underlying both processes.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 252 (1965), S. 1-8 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Lidoflazine, a new and very longacting coronary vasodilator was given to 18 dogs with a chronically developing stenosis and occlusion of the circumflex coronary artery for 4 and 6 weeks respectively. 18 other dogs with chronically developing stenoses leading to occlusion of the circumflex artery were used as controls. Lidoflazine in a dosis of 20 mg/kg/day increased the speed of development of the collateral circulation and prohibited symptoms of permanent cardiac hypoxia. Permanent myocardial hypoxia, caused by a higher degree of physical activity in a group of “freely exercising” dogs produced the same favorable effects on the canine coronary collateral circulation.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 361 (1973), S. 263-282 
    ISSN: 1432-2307
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Light microscopic and ultrastructural changes in developing coronary collateral vessels were investigated after treatment with hydrocortisone (20 mg/kg/day orally) in the dog. The expected inflammatory reaction in the early stage of development (3 weeks) was absent, signs of injury to the vascular wall were lacking. At 3 and 8 weeks proliferation of rough and smooth endoplasmic reticulum and of the Golgi field was prominent indicating changes in the metabolism of the cells. The amount of extracellular MPS, collagen and new elastic material was decreased. Intimal hyperplasia occurred at the same rate in the treated as in the untreated animals. At 3 months the vascular architecture was restored, cellular hyperactivity had decreased. It is concluded from these results that: 1. Only collaterals in the acute stage of growth are influenced by treatment with hydrocortisone. 2. When collateral growth had come to a standstill, an influence of hydrocortisone was no longer demonstrable. 3. Normal non-growing coronary arteries in normal hearts and in those with coronary occlusion are not influenced by hydrocortisone.
    Type of Medium: Electronic Resource
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  • 17
    ISSN: 1432-0878
    Keywords: Key words: Mitosis ; Gene expression ; Histone H3 ; PCNA (proliferating cell nuclear antigen) ; Microembolization ; Angiogenesis ; Pig (Landrace)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. In ischaemic porcine myocardium, the growth of collateral vessels by angiogenesis is observed in clusters in the vicinity of focal necroses. Because mitosis of endothelial cells is a prerequisite for angiogenesis, the purpose of this study has been to evaluate the time course of mitosis as an indicator of vascular growth in a porcine model of coronary microembolization. Ischaemia was induced by injection of 25-µm microspheres in the left circumflex artery, followed by tissue collection from non-ischaemic and ischaemic areas of the same heart after 24, 72 or 168 h microembolization. Tissue was studied by histone H3 in-situ hybridization, PCNA/cyclin immunohistochemistry and electron microscopy. The number of blood vessels in ischaemic myocardium was compared with that in normal control tissue. Capillary growth started as early as 24 h after microembolization, as indicated by increasing numbers of proliferating, histone H3- and PCNA/cyclin-positive cells in the necrotic inflammatory foci of the ischaemic area. At 72 h and 168 h, the number of blood vessels was significantly higher in ischaemic than in normal myocardium, whereas at 168 h, mitosis of cells was, as in normal myocardium, a rare event. Coronary microembolization of porcine myocardium thus leads to an increased cellular proliferation rate between 24 h and less than 7 days after the onset of microembolization, followed by enhanced capillary growth. In-situ hybridization with histone H3 and PCNA/cyclin immunohistochemistry seem to be reliable markers for proliferation and vascular growth in non-cancerogenic tissue.
    Type of Medium: Electronic Resource
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  • 18
    ISSN: 1432-0878
    Keywords: Key words: Adhesion molecules ; Human umbilical vein endothelial cells ; Cytokines ; Cell culture ; Immunohistochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. The time course of expression of the adhesion molecules E-selectin, VCAM-1, ICAM-1 and PECAM-1 was studied in interleukin-1β-stimulated human umbilical vein cells (HUVEC) and the subcellular sites of synthesis were determined by means of fluorescence immunohistochemistry. The maximal number of cells labelled for E-selectin was observed at 2–4 h, for VCAM-1 at 4–8 h and ICAM-1 at 6–72 h. At 8 h, E-selectin and VCAM-1 started to disappear, but ICAM-1-positive cells persisted. PECAM-1 was constitutively expressed. De novo synthesis for E-selectin started at 1 h and for both, VCAM-1 and ICAM-1 at 1.5–2 h. Maximal synthetic activity was observed at 2.5–4 h for E-selectin and at 4–6 h for VCAM-1 and ICAM-1; thereafter, synthesis slowly decreased. Transport granules occurred at 1.5 h for E-selectin and 4 h for VCAM-1; they were absent for ICAM-1. Diffuse cellular and membrane labelling indicative of the functional activity of the adhesion molecules began at 2–4 h for E-selectin, and 4 h for VCAM, but was constitutively present for ICAM-1. In conclusion, each adhesion molecule shows a specific time-dependent course of appearance and disappearance in interleukin-1β-stimulated HUVECs in accordance with their physiological role in vivo. These morphological results confirm data obtained by flow cytometry and Western blotting, but they provide new information about the behaviour of individual cells with regard to the sites of synthesis and cellular localization of the adhesion molecules.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thrombosis and thrombolysis 4 (1997), S. 113-116 
    ISSN: 1573-742X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    Cardiovascular drugs and therapy 2 (1988), S. 17-25 
    ISSN: 1573-7241
    Keywords: ischemia ; reperfusion ; myocardial infarction ; ultrastructure ; necrosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The time course of myocardial ischemia was studied in canine myocardium by electron microscopy. Ischemia of the myocardium produces ultrastructural alterations of mitochondria, nuclei, contractile apparatus, and the SR- and T-tubular system that are accompanied by loss of glycogen and intracellular edema. These changes are more pronounced with increasing severity of ischemia, and they allow the differentiation between different stages of reversible and of irreversible injury. Reperfusion of reversibly injured tissue leads to structural recovery; reperfusion of irreversibly injured tissue produces further deterioration. On the basis of ultrastructural data, it was found that in a dog, after 45 minutes of coronary artery occlusion, subendocardial infarction was present in 20% of all animals. Transmural infarction was present in 24% of all dogs after 90 minutes of coronary artery occlusion and in 53% after 24 hours. The individual variability in the speed of development of infarction is caused by the rate of oxygen consumption at the time of occlusion and by the amount of collateral flow. Intermittent ischemia is much better tolerated than permanent ischemia of the same duration. Species differences are evident. The course of development of myocardial necrosis, therefore, depends on time, rate of oxygen consumption, collateral flow, mode of ischemia, and on the species investigated.
    Type of Medium: Electronic Resource
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