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  • S. Karger AG  (7)
  • 2000-2004  (7)
  • 1
    Online Resource
    Online Resource
    S. Karger AG ; 2002
    In:  Digestion Vol. 65, No. 1 ( 2002), p. 47-55
    In: Digestion, S. Karger AG, Vol. 65, No. 1 ( 2002), p. 47-55
    Abstract: 〈 i 〉 Background/Aims: 〈 /i 〉 Treatment of isolated pancreatic acini with high concentrations of cholecystokinin (CCK) is known to induce rapid changes in the cellular morphology. The signalling pathways remain to be characterized. 〈 i 〉 Methods: 〈 /i 〉 Pancreatic acini were permeabilized by digitonin and incubated with various agents. The acinar morphology was investigated by microscopy. The activation of p125 focal adhesion kinase was determined by Western blot analysis. Amylase was measured photometrically. 〈 i 〉 Results: 〈 /i 〉 The functionality of the permeabilized acini was tested by measuring stimulated amylase release. 300 µ 〈 i 〉 M 〈 /i 〉 GTPγS was almost as efficient as CCK to stimulate amylase release, while 300 µ 〈 i 〉 M 〈 /i 〉 GDPβS inhibited the CCK-stimulated amylase release. Stimulation of permeabilized acini with 0.1 µ 〈 i 〉 M 〈 /i 〉 CCK induced similar morphological changes as in unpermeabilized acini. Incubation of permeabilized acini with GTPγS mimicked the CCK-induced changes, whereas a preincubation with GDPβS prevented the CCK effects on the acinar morphology. Inhibition of the small G protein rho, which activates p125 focal adhesion kinase, by 〈 i 〉 Clostridium botulinum 〈 /i 〉 C3 transferase also prevented the CCK-stimulated morphological changes. Preincubation of intact acini with cell-permeable inhibitors of protein kinase C, MEK or p38MAPK, or with the intracellular calcium chelator BAPTA/AM was without significant effect on the CCK-stimulated changes. 〈 i 〉 Conclusion: 〈 /i 〉 The CCK-induced morphological changes seem to be mediated by G protein signalling via the small G protein rho and the associated activation of p125 focal adhesion kinase.
    Type of Medium: Online Resource
    ISSN: 0012-2823 , 1421-9867
    RVK:
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2002
    detail.hit.zdb_id: 1482218-0
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  • 2
    In: Digestion, S. Karger AG, Vol. 64, No. 3 ( 2001), p. 169-178
    Abstract: 〈 i 〉 Background/Aims: 〈 /i 〉 The lectin phytohemagglutinin is a mitogen for intestinal epithelial cells in vivo. The mechanisms of action are unknown and were therefore analyzed in vitro. 〈 i 〉 Methods: 〈 /i 〉 Human (Intestine-407) and rat (IEC-6; IEC-18) intestinal epithelial cell lines were stimulated with phytohemagglutinin. Proliferation was assayed by 〈 sup 〉 3 〈 /sup 〉 H-thymidine incorporation, activation of mitogen-activated protein kinase (MAPK) by Western blotting, and induction of c-fos mRNA expression by semiquantitative polymerase chain reaction. Control experiments were performed with phenyl-N-acetyl-α- 〈 i 〉 D 〈 /i 〉 -galactosaminide or the tyrosine kinase inhibitor tyrphostin A25. 〈 i 〉 Results: 〈 /i 〉 Phytohemagglutinin (0.1 µg/ml) significantly stimulated proliferation in all three cell lines after 48–72 h. MAPK activation was detected after 15–30 min, and an induction of c-fos mRNA expression after 15– 30 min of stimulation. Mitogenic effects were blocked by preincubation with phenyl-N-acetyl-α- 〈 i 〉 D 〈 /i 〉 -galactosaminide or tyrphostin A25. 〈 i 〉 Conclusion: 〈 /i 〉 Phytohemagglutinin stimulated proliferation, MAPK activation and induction of c-fos mRNA expression. The lectin may contribute to intestinal mucosal growth and regeneration thereby preventing gut atrophy.
    Type of Medium: Online Resource
    ISSN: 0012-2823 , 1421-9867
    RVK:
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2001
    detail.hit.zdb_id: 1482218-0
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  • 3
    In: Neuroepidemiology, S. Karger AG, Vol. 22, No. 4 ( 2003), p. 255-264
    Abstract: 〈 i 〉 Background and Purpose: 〈 /i 〉 Limited information can be obtained as to the availability of neurological in-patient services in the former communist countries of Eastern and Central Europe. The objective was to analyse data received directly from representatives of the particular countries. 〈 i 〉 Methods: 〈 /i 〉 The data were collected under the auspices of the ‘First European Cooperation Neurology Workshop’ held in April 2000, in Třešť, Czech Republic. Neurologists from 15 post-communist countries provided information from their respective countries. Linear trends in graphs including the reliability value R 〈 sup 〉 2 〈 /sup 〉 were used in the analysis of correlations. 〈 i 〉 Results: 〈 /i 〉 Data from 14 countries were assembled and trends were analysed. 〈 i 〉 Conclusions: 〈 /i 〉 Direct relationships were found between: (1) the average department size and the average catchment area (R 〈 sup 〉 2 〈 /sup 〉 = 0.1015); (2) the percentage of districts with a neurological in-patient department and the gross national product (GNP) per capita (R 〈 sup 〉 2 〈 /sup 〉 = 0.1359); (3) the average neurological department size and the GNP per capita (R 〈 sup 〉 2 〈 /sup 〉 = 0.1135), and (4) the average length of treatment and the number of neurological beds/100,000 inhabitants (R 〈 sup 〉 2 〈 /sup 〉 = 0.1745). Inverse relationships were found between: (1) the number of neurological beds/100,000 inhabitants and the average hospital catchment area (R 〈 sup 〉 2 〈 /sup 〉 = 0.2105), and (2) the number of neurological beds/100,000 inhabitants and the GNP per capita (R 〈 sup 〉 2 〈 /sup 〉 = 0.1144).
    Type of Medium: Online Resource
    ISSN: 0251-5350 , 1423-0208
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2003
    detail.hit.zdb_id: 1483032-2
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  • 4
    In: Cerebrovascular Diseases, S. Karger AG, Vol. 15, No. 1-2 ( 2003), p. 22-28
    Abstract: 〈 i 〉 Background and Purpose: 〈 /i 〉 Chronic alcohol intake is considered to be a risk factor for spontaneous intracranial hemorrhage (SICH). However, there is a lack of objective data in this field. The aim was to assess its role in hemorrhagic stroke objectively and to evaluate its correlation with the elevation of γ-glutamyltransferase (GGT) plasma levels. The reliability of patients’ anamnestic data concerning alcohol intake was also assessed. 〈 i 〉 Methods: 〈 /i 〉 Laboratory assessment of the plasma carbohydrate-deficient transferrin (CDT) level was performed in 105 SICH patients and in a control group of 105 patients with dorsalgia. All patients were treated at the Clinic of Neurology, Faculty Hospital, Olomouc, Czech Republic. GGT plasma level values and anamnestic data concerning alcohol consumption were also analyzed. χ 〈 sup 〉 2 〈 /sup 〉 tests were applied when assessing statistical significance. 〈 i 〉 Results: 〈 /i 〉 The CDT test was positive in 25.7% of SICH patients versus 7.6% of control group subjects (p = 0.0008). GGT plasma levels were elevated in 44.4% of SICH patients with a positive CDT test versus 25.6% of patients with a negative one. The GGT test is not reliable in the detection of alcohol intake when compared with the CDT test (p = 0.71). Only 13.0% of SICH patients with a positive CDT test (subgroup 1) stated regular and high consumption of all types of alcoholic beverages. Another 26.1% of these patients stated regular daily consumption of more than 1 liter, and 47.8% of them stated less than 1 liter of beer, with uncertain data concerning wine and spirits intake. Thirteen percent of subgroup 1 patients denied alcohol consumption altogether. 〈 i 〉 Conclusions: 〈 /i 〉 Chronic alcohol consumption is at least one of several risk factors in one fourth of SICH patients in the Olomouc region of the Czech Republic. The CDT test is the most sensitive method to diagnose chronic alcohol consumption, and it is superior to the examination of GGT and the evaluation of patients’ anamnestic data.
    Type of Medium: Online Resource
    ISSN: 1015-9770 , 1421-9786
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2003
    detail.hit.zdb_id: 1482069-9
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  • 5
    Online Resource
    Online Resource
    S. Karger AG ; 2002
    In:  Transfusion Medicine and Hemotherapy Vol. 29, No. 5 ( 2002), p. 254-258
    In: Transfusion Medicine and Hemotherapy, S. Karger AG, Vol. 29, No. 5 ( 2002), p. 254-258
    Type of Medium: Online Resource
    ISSN: 1660-3796 , 1660-3818
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2002
    detail.hit.zdb_id: 2100533-3
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  • 6
    In: Digestion, S. Karger AG, Vol. 61, No. 4 ( 2000), p. 237-246
    Abstract: 〈 i 〉 Background: 〈 /i 〉 Hepatocyte growth factor (HGF) stimulates proliferation, migration and morphogenesis of epithelial cells by specific binding to its receptor c-met. Overexpression of HGF or c-met has been reported for human gastric or pancreatic cancer. In colorectal cancer overexpression of c-met but not HGF has been shown. However, elevated HGF serum levels have been detected in colorectal cancer patients. Therefore, the present study was performed to investigate expression patterns of both c-met and HGF in colorectal cancers and metastasis in comparison to normal mucosa. Furthermore, the mitogenic actions of HGF on colorectal cancer cells were studied in vitro. 〈 i 〉 Methods: 〈 /i 〉 Expression of c-met and HGF were analyzed by RT-PCR and Western blotting and localized in the tissues utilizing immunohistochemistry. Mitogenic effects of HGF were determined in four human colon cancer cell lines by 〈 sup 〉 3 〈 /sup 〉 H-thymidine incorporation studies. 〈 i 〉 Results: 〈 /i 〉 C-met and HGF mRNA were detectable in 60% of the normal specimen, but in the majority of cancer samples, and in just 33% of the liver metastasis. In cancer samples a coexpression of c-met and HGF was detected in 77% of the specimens. The extent of protein expression of receptor and ligand correlated with the mRNA expression. Moreover, c-met protein expression was increased 2- to 3-fold in colorectal cancers. C-met was detected in cells of epithelial origin, whereas HGF was expressed by mesenchymal cells. In vitro, HGF significantly stimulated cell growth in all four cell lines. 〈 i 〉 Conclusion: 〈 /i 〉 Overexpression of c-met protein in colorectal cancers is combined with an expression of HGF in the majority of cases suggesting a paracrine manner of growth enhancement, while only a weak expression of c-met or HGF was detected in metastatic tissues.
    Type of Medium: Online Resource
    ISSN: 0012-2823 , 1421-9867
    RVK:
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2000
    detail.hit.zdb_id: 1482218-0
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  • 7
    Online Resource
    Online Resource
    S. Karger AG ; 2000
    In:  Digestion Vol. 61, No. 4 ( 2000), p. 257-310
    In: Digestion, S. Karger AG, Vol. 61, No. 4 ( 2000), p. 257-310
    Type of Medium: Online Resource
    ISSN: 0012-2823 , 1421-9867
    RVK:
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2000
    detail.hit.zdb_id: 1482218-0
    Library Location Call Number Volume/Issue/Year Availability
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