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  • 1990-1994  (4)
  • Anterior horn cell  (1)
  • Bleeding site  (1)
  • Cytochromec oxidase
  • Gene expression
  • Physics
  • 1
    ISSN: 1433-2981
    Keywords: Abdominal aorta ; Bleeding site ; Coagulation ; Haematology ; Inferior vena cava ; Orbital venous plexus ; Plasma chemistry ; Rats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Of paramount importance to most toxicity studies in rats is the evaluation of haematological, coagulation and clinical chemistry parameters. In European and North American countries, the orbital venous plexus (OVP) is currently the most common route for obtaining blood, whereas in Japan the inferior vena cava (IVC) and abdominal aorta (AA) are the preferred routes. In order to compare clinical pathology parameters from the three bleeding sites, 11-week-old male F344 rats were anaesthetised by ether inhalation, and blood samples collected by IVC, AA or OVP for subsequent haematological, coagulation and plasma chemistry analysis. Collection methods utilised a plastic (5 ml) syringe and needle for IVC and AA, and glass capillary tubes (1.5 mm × 30 mm) for OVP. Ten haematology parameters, two coagulation and 22 plasma chemistry parameters were assayed, and the results compared between the three bleeding sites. The results showed there were no essential differences in the haematological or plasma chemistry values when blood was withdrawn from either the IVC or OVP. However, blood collected from the AA exhibited white cell counts of only 40%\2-60% of the values from the other two sites, and plasma glucose values showed slightly higher values. Other haematological, coagulation and plasma chemistry values showed no meaningful differences between the three bleeding sites, any differences being small and not considered to be biologically or clinically significant. Although some values may vary with the selection of bleeding site, careful and gentle sampling, avoiding stress and artefacts (e.g. tissue fluid) will minimise these differences. It is important therefore that clinical pathology assays during the course of a toxicity study should use the same sample site, preanalytical conditions and analytical methods. The results obtained in this study will be used as baseline data for haematology and clinical chemistry characteristics for the three bleeding sites in male F344 rats.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0533
    Keywords: Joseph's disease ; Ubiquitin ; Immunocytochemistry ; Anterior horn cell ; Hypoglossal nucleus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We describe a patient with progressive spastic ataxia and ophthalmoparesis. His clinical and neuropathological findings were consistent with Joseph's disease. The most characteristic neuropathological features in the present case were ubiquitin-immunoreactive filamentous or dense inclusions in spinal anterior horn cells and hypoglossal neurons, which have been considered to be a specific finding in amyotrophic lateral sclerosis (ALS). The occurrence of ubiquitin-immunoreactive inclusions suggests that such inclusions are not totally specific to ALS and could occur in occasional degenerating motor neurons without apparent ALS neuropathology.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0533
    Keywords: In situ hybridization ; Mitochondrial DNA ; Mitochondrial myopathy ; Ophthalmoplegia ; Cytochromec oxidase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary To determine whether a mitochondrial mRNA deficiency exists in mitochondrial myopathies, muscle biopsies from a patient with chronic progressive external ophthalmoplegia (CPEO) and a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) were studied using in situ hybridization. Histochemistry and immunohistochemistry were performed along with hybridization. Hybridization reactions were widely distributed over the sarcoplasm of all muscle fibers in the patient with MELAS. In the patient with CPEO, 80% of the fibers showed a marked decrease in density of autoradiographic grains. This marked decrease corresponded to the histochemical and immunohistochemical findings of a very weak staining of cytochromec oxidase (CCO). The isotope-labeled cDNA probe used in in situ hybridization in this study complements a part of subunit I of CCO and a part of subunit II of complex I in the mitochondrial gene. Our results suggest a defect in the mRNA in this CPEO patient.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-069X
    Keywords: Gene expression ; TNF-α ; HSP70 ; BehÇet's disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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