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  • 1
    Keywords: Forschungsbericht ; Knochenbruch ; Osteoporose ; Therapieerfolg ; Enzymstoffwechsel ; Hormonstoffwechsel ; Estradiol ; Testosteron
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (20 Seiten, 390,13 KB)
    Language: German
    Note: Förderkennzeichen BMBF 031A467C. - Verbund-Nummer 01154597 , Projektleiter und Stellvertreter sind laut Berichtsblatt Autor , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden , Sprache der Zusammenfassung: Deutsch, Englisch
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  • 2
    Online Resource
    Online Resource
    Milton :Taylor & Francis Group,
    Keywords: Microcirculation disorders. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (513 pages)
    Edition: 1st ed.
    ISBN: 9780429523434
    Series Statement: Routledge Revivals Series
    DDC: 612.135
    Language: English
    Note: Cover -- Title Page -- Copyright Page -- THE EDITORS -- FOREWORD -- DEDICATION -- ACKNOWLEDGMENTS -- PREFACE -- CONTRIBUTORS -- Table of Contetns -- Section I: Introduction -- Chapter 1: The Microcirculation and Clinical Disease -- Section II: Clinical Syndromes and the Microcirculation -- Chapter 2: Atherosclerosis and the Microcirculation -- Chapter 3: Diabetes and the Microcirculation -- Chapter 4: Hypertension and the Microcirculation -- Chapter 5: Shock and Multiple-Organ Dysfunction and the Microcirculation -- Chapter 6: Leukocyte/Endothelial Cell Adhesion and Ischemia/Reperfusion Injury -- Chapter 7: Adult Respiratory Distress Syndrome and the Microcirculation -- Chapter 8: Malignant Tumors and the Microcirculation -- Section III: Development of Microcirculation Research -- Chapter 9: Historical Aspects of Microcirculation Research -- Chapter 10: Technological Developments in the Study of the Microcirculation -- Chapter 11: Application of Microcirculation Research to Clinical Disease -- Section IV: Specific Application of Microcirculation Research -- Chapter 12: Bone Microcirculation -- Chapter 13: Brain Microcirculation -- Chapter 14: Eye Microcirculation -- Chapter 15: Stomach Microcirculation -- Chapter 16: Heart Microcirculation -- Chapter 17: Intestine Microcirculation -- Chapter 18: Kidney Microcirculation -- Chapter 19: Liver Microcirculation -- Chapter 20: Lung Microcirculation -- Chapter 21: Peripheral Nerve Microcirculation -- Chapter 22: Pancreas Microcirculation -- Chapter 23: Skeletal Muscle Microcirculation -- Chapter 24: Skin Microcirculation -- Chapter 25: Spleen Microcirculation -- Chapter 26: Thyroid Microcirculation -- Chapter 27: Urinary Bladder Microcirculation -- Section V: Functional Components of the Microcirculation -- Chapter 28: Angiogenesis -- Chapter 29: Blood Cells and Rheology -- Chapter 30: Endothelial Cells. , Chapter 31: Interstitium and Lymphatics -- Chapter 32: Isolated, Perfused Microvessels -- Chapter 33: Microvascular Architecture and Networks -- Chapter 34: Vascular Smooth Muscle Cells -- Index.
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  • 3
    ISSN: 1432-2277
    Keywords: Preservation, liver, warm rinse ; Ringer's lactate, warm, liver preservation ; Liver, warm rinse, preservation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This quantitative in vivo fluorescence microscopy study investigated the impact of warm versus cold Ringer's lactate (RL) graft rinse on various microvascular manifestations of ischemia-reperfusion injury after liver translantation in the rat. Syngeneic orthotopic liver transplantation, including arterial revascularization, was performed in male Lewis rats following 24 h of cold storage in University of Wisconsin (UW) solution. In one group (n=8) liver grafts were rinsed with 4°C (cold) RL, whereas in the other group (n=8) grafts were rinsed with 37°C (warm) RL immediately prior to revascularization. Hepatic microvascular perfusion, leukocyteendothelium interaction, and Kupffer cell activation were quantified 30–90 min after graft reperfusion by direct visualization with intravital fluorescence microscopy. Moreover, biliary excretory graft function was analyzed by determination of bile flow and bile salt excretion during the first 90 min after reperfusion. Compared to grafts rinsed with cold RL, acinar and sinusoidal perfusion were found to be significantly increased after rinsing the grafts with warm RL. The amount of nonperfused acini declined from 18.1%±4.0% to 7.4%±1.6% (P〈0.05), and the total percentage of perfused sinusoids increased from 80.1±1.4 to 88.4±1.2 (P〈0.001) after cold and warm rinse, respectively. After rinsing the graft with warm RL, WBC adherence in sinusoids and especially in postsinusoidal venules decreased significantly by 28% (P〈0.001) and 33% (P〈0.001), respectively. Kupffer cell activation was markedly reduced after rinsing with RL at 37°C, as indicated by a decelerated adherence of latex particles injected 80 min after reperfusion. Excretory graft function was dramatically increased following warm RL rinse during the 90-min observation period. Bile flow was enhanced from 1.04±0.5 to 3.9±0.8 ml/100 g liver per 90 min (P〈0.01), with a parallel rise in bile salt excretion from 24.3±5.8 to 128.0±19.8 mmol/100 g liver per 90 min (P〈0.05) when compared to cold RL. These data strongly suggest that rinsing liver grafts with warm RL prior to reperfusion represents a simple and inexpensive way to reduce the incidence of primary graft failure secondary to ischemia and reperfusion injury in liver transplantation.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1262
    Keywords: Microcirculation Sinusoidal diameter pO2 Carbon tetrachloride Hepatic arterial buffer response
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. We investigated sinusoidal blood flow and hepatic tissue oxygenation during portal vein occlusion in cirrhotic rat livers to examine the effect of cirrhosis on the properties of hepatic microvascular blood flow regulation. After 8 weeks of CCl4/phenobarbital sodium treatment to induce cirrhosis Sprague-Dawley rats were prepared surgically to allow assessment of portal venous and hepatic arterial inflow using miniaturized flow probes with simultaneous analysis of hepatic microcirculation and tissue oxygenation by fluorescence microscopy and polarographic oxymetry. Age-matched noncirrhotic animals served as controls. Upon portal vein occlusion in cirrhotic livers (flow reduction to 〈20%), hepatic arterial blood flow increased 1.5-fold (61±8 ml/min per 100 g liver) of baseline (40±7 ml/min per 100 g liver), reflecting an appropriate hepatic arterial buffer response (HABR), similarly as seen in control livers. The net result was a reduction in total liver inflow from 90±12 to 72±11 ml/min per 100 g liver, which was associated with a significant decrease in both sinusoidal red blood cell velocity and volumetric blood flow to approx. 71% and 76% of baseline values. However, portal vein occlusion did not cause a deterioration in hepatic tissue pO2 (11±3 vs. 10±3 mmHg at baseline). Sinusoidal diameters were found unchanged, disproving a major role of the sinusoidal tone in the regulation of HABR. Microvascular response of cirrhotic livers did not generally differ from that in noncirrhotic livers upon portal inflow restriction. We conclude that HABR in cirrhotic livers operates sufficiently to meet the liver tissue oxygen demand, most probably by an increased relative contribution of arterial perfusion of hepatic sinusoids.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-2277
    Keywords: Key words Non-heart-beating donors ; Liver ; Microvascular preservation ; Heparin ; Phentolamine ; Warm ischemia time
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Improvement of organ procurement from non-heart-beating donors (NHBDs) could increase the donor organ pool for liver transplantation. Whether anti-coagulative and anti-vasospastic substances can improve hepatic microvascular preservation from NHBDs is unknown. In donor rats which were pretreated with either heparin (n = 6) or heparin combined with phentolamine (n = 7) 10 min prior to cardiac arrest, the extent and homogeneity of hepatic microvascular reperfusion was assessed at the end of a 60-min period of cardiac arrest using in situ fluorescence microscopy. Non-pretreated animals with cardiac arrest for 60 min served as controls (n = 6). In the non-treated NHBDs, arterial gravity perfusion of 100 cm H2O with HTK-solution led to a hepatic acinar reperfusion of only ∼ 22 % with a remarkably diminished sinusoidal density. Application of heparin prior to cardiac arrest resulted in a two-fold, but insignificant increase of acinar perfusion and sinusoidal density with a still considerable heterogeneity of both parameters. Livers of NHBDs that additionally received phentolamine exhibited significantly increased values of both acinar perfusion and sinusoidal density. Phentolamine was found to reduce heterogeneity of organ microperfusion. Thus, our results indicate that the combined application of heparin and phentolamine is a useful additive for optimizing the quality of organs harvested from NHBDs.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neuro-oncology 50 (2000), S. 99-108 
    ISSN: 1573-7373
    Keywords: brain tumor ; vessels ; endothelial cells ; pericytes ; perfusion ; micorcirculation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Structural and functional abnormalities of the vascular microenvironment determine pathophysiological characteristics of gliomas, such as loss of blood–brain barrier function, tumor cell invasiveness, or permselectivity for large molecules. Moreover, the effectiveness of various therapeutic strategies critically depends upon the successful transvascular delivery of molecules. In order to shed more light on the vascular microenvironment in gliomas, a variety of experimental and clinical techniques have been applied to study the glioma microvasculature, including histology, vascular corrosion casts, microangiography by injection of dyes, blood flow measurements by autoradiography, tracer washout techniques, magnetic resonance imaging, as well as intravital fluorescence microscopy. This review summarizes the characteristic features of vascular morphology, angio-architecture, tumor perfusion, microvascular permeability, as well as microvessel-related immunological competence in gliomas. An improved understanding of the vascular microenvironment in gliomas will help in the future to optimize glioma imaging and delivery of vectors for gene therapy or encapsulated drug carriers in patients.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Langenbeck's archives of surgery 385 (2000), S. 42-49 
    ISSN: 1435-2451
    Keywords: Key words Topical drug application ; Liposomes ; Buflomedil hydrochloride ; Wound healing ; Epithelialization ; Neovascularization ; Hairless mouse ; Intravital fluorescence microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Background: Despite intensive research, impaired wound healing remains a considerable complication. Therefore, topically applied liposome-encapsulated buflomedil hydrochloride was investigated for its ability to improve wound repair in normal (n=16) and ischemic (n=16) skin tissue. Methods: Experiments were performed using the wound healing model of the ear of hairless mice. Standardized skin wounds (4.25 mm2) were created by circular excision of the epidermal layer and the subcutaneous tissue. Liposomes were applied daily until complete neovascularization of the wound occurred. Tissue regeneration by complete epithelialization and neovascularization of the wound area, microcirculatory parameters, and leukocyte–endothelium interaction were investigated by means of intravital microscopy. Microvascular perfusion was assessed by laser-Doppler flowmetry. Results: Topical application of buflomedil liposomes led to a significantly (P〈0.05) accelerated wound closure in both normal (9.6±0.7 days) and ischemic (13.4±0.1 days) skin tissue compared with animals that were treated with unloaded liposomes (controls; 13.1±0.8 days; 15.3±0.6 days). Complete neovascularization of the wound was also enhanced (P〈0.05) in buflomedil-treated animals (normal tissue 18.8±0.4 days; ischemic tissue 19.6±0.7 days) compared with controls (20.6±0.6 days; 22.6±1.2 days). Conclusion: These data suggest that buflomedil-loaded liposomes might be of beneficial use for clinical wound care.
    Type of Medium: Electronic Resource
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