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  • 1
    In: Nephron Clinical Practice, S. Karger AG, Vol. 123, No. 3-4 ( 2013-8-6), p. 202-208
    Abstract: 〈 b 〉 〈 i 〉 Background/Aims: 〈 /i 〉 〈 /b 〉 S100A12 induces vascular inflammation contributing to the development of atherosclerosis. Serum S100A12 concentration is shown to be elevated in patients with chronic kidney disease (CKD), however the reason remains unclear. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 Transcriptional levels of S100A12 and RAGE (receptor for advanced glycation end products) were measured in peripheral leukocytes by quantitative real-time RT-PCR. Subjects were 40 patients with CKD stage 4-5, 20 of whom were affected with cardiovascular disease (CVD), and 20 healthy subjects. Serum concentrations of S100A12 and soluble RAGE were measured using enzyme-linked immunosorbent assay. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 The serum concentration of S100A12 was significantly higher in CKD patients than in healthy subjects 〈 b 〉 〈 /b 〉 (78.5 ± 70.5 vs. 23.7 ± 19.2 ng/ml, p = 0.0035), but that of soluble RAGE was not. 〈 b 〉 〈 /b 〉 The relative quantity of 〈 b 〉 〈 /b 〉 S100A12 mRNA was significantly greater in leukocytes from CKD patients than in those from healthy subjects [mean (95% confidence interval of the mean): 3.1 (2.2-3.9) vs. 1.2 (0.8-1.7), p = 0.0001], however that of RAGE mRNA was not. The serum concentration of S100A12 was significantly correlated with the relative quantity of S100A12 mRNA among uremic CKD patients (r 〈 sup 〉 2 〈 /sup 〉 = 0.656, p 〈 0.0001). Both the serum concentration and gene expression of S100A12 were significantly higher in patients who had CVD than in those who did not. 〈 b 〉 〈 i 〉 Conclusion: 〈 /i 〉 〈 /b 〉 Excessive expression of 〈 b 〉 〈 /b 〉 the 〈 b 〉 〈 /b 〉 S100A12 gene in uremic leukocytes is relevant to its increased serum concentration, particularly in those affected with CVD.
    Type of Medium: Online Resource
    ISSN: 1660-2110
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2013
    detail.hit.zdb_id: 2098336-0
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  • 2
    In: European Neurology, S. Karger AG, Vol. 62, No. 5 ( 2009), p. 274-280
    Abstract: 〈 i 〉 Objective: 〈 /i 〉 To investigate clinical and magnetic resonance imaging (MRI) features of Wernicke’s encephalopathy with cortical abnormalities (WEc). 〈 i 〉 Methods: 〈 /i 〉 We retrospectively evaluated the clinical features and MRI findings in 3 cases of WEc in comparison with those of 7 previously reported cases. 〈 i 〉 Results: 〈 /i 〉 Besides the classical triad of ocular abnormalities, ataxia and global confusion, muscular weakness of all extremities was frequently recognized (5 of 6 evaluable cases; 83%). During the clinical courses, 2 patients (20%) died and 1 fell into a vegetative state. The cortical abnormalities were distributed in the frontal and parietal lobes, especially around the bilateral central sulcus, in all cases. In 1 case, the cortical abnormality was irreversible, and the abnormal lesion, similar to that seen in laminar necrosis, persisted. 〈 i 〉 Conclusions: 〈 /i 〉 Bilateral frontal cortical abnormalities around the central sulcus and muscular weakness of all extremities might be the characteristic features of WEc.
    Type of Medium: Online Resource
    ISSN: 0014-3022 , 1421-9913
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2009
    detail.hit.zdb_id: 1482237-4
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  • 3
    Online Resource
    Online Resource
    S. Karger AG ; 1998
    In:  International Archives of Allergy and Immunology Vol. 117, No. 3 ( 1998), p. 202-208
    In: International Archives of Allergy and Immunology, S. Karger AG, Vol. 117, No. 3 ( 1998), p. 202-208
    Abstract: 〈 b 〉 Background: 〈 /b 〉 Studies have shown the importance of apoptosis in vascular injury in vitro. We postulated that apoptosis of the endothelium contributes to vascular injury in vivo and may be involved in acute lung injury. 〈 b 〉 Methods: 〈 /b 〉 To test this hypothesis, we investigated the incidence of endothelial cell apoptosis in acute lung injury induced in mice by the administration of lipopolysaccharide (LPS). Male ICR mice were administered LPS (20 mg/kg body weight) intravenously and sacrificed at specified times thereafter. 〈 b 〉 Results: 〈 /b 〉 Histologic findings were consistent with acute lung injury which increased with time from 3 to 48 h after injection. Electrophoretic analysis of DNA that was extracted from lung tissue and 3'–end–labeled with digoxigenin demonstrated a fragmentation of DNA starting at 6 h. In situ terminal deoxynucleotidyl transferase–mediated dUTP biotin nick end–labeling (TUNEL) demonstrated DNA strand breaks in the endothelial cells. TUNEL also revealed DNA strand breaks in bronchial and alveolar epithelial cells as well as inflammatory cells in the interstitium. These TUNEL–positive cells appeared 6 h after injection. Electron–microscopic examination of the endothelium strongly suggested the morphological characteristics of apoptosis. 〈 b 〉 Conclusion: 〈 /b 〉 Apoptosis was induced by LPS administration in endothelial cells in vivo. A role for such apoptosis is suggested in acute lung injury.
    Type of Medium: Online Resource
    ISSN: 1018-2438 , 1423-0097
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 1998
    detail.hit.zdb_id: 1482722-0
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  • 4
    In: International Archives of Allergy and Immunology, S. Karger AG, Vol. 116, No. 4 ( 1998), p. 306-312
    Abstract: 〈 b 〉 Background: 〈 /b 〉 The bleomycin–induced pneumopathy involves a T cell–mediated immune response. T cell activation requires both antigen/MHC recognition and costimulatory signals. The CD28 receptor on T cells with its ligand B7 represents one of the most important examples of this costimulation. Interleukin 12 (IL–12) has a strong synergistic effect with the B7–1/CD28 interaction on inducing proliferation and cytokine production in T cells. 〈 b 〉 Methods: 〈 /b 〉 In this study, we investigated the expression of B7–1, B7–2, and IL–12 in bleomycin–induced pneumopathy in mice using reverse transcription polymerase chain reaction (RT–PCR), RT in situ PCR, and immunohistochemistry. 〈 b 〉 Results: 〈 /b 〉 We observed concurrent upregulation of B7–1, B7–2, and IL–12p40 mRNA in the lung tissues at 1 h to 7 days after bleomycin instillation into the trachea. B7–1 mRNA and protein were found in bronchiolar epithelial cells as well as macrophages, B7–2 and IL–12p40 mRNA appeared to be expressed in mononuclear cells. 〈 b 〉 Conclusions: 〈 /b 〉 These findings indicate that T cell–mediated immune response in this model involves the upregulation of B7–1, B7–2, and IL–12p40 mRNA, and also demonstrate the aberrant expression of B7–1 in bronchiolar epithelial cells.
    Type of Medium: Online Resource
    ISSN: 1018-2438 , 1423-0097
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 1998
    detail.hit.zdb_id: 1482722-0
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  • 5
    In: International Archives of Allergy and Immunology, S. Karger AG, Vol. 140, No. 4 ( 2006), p. 327-333
    Abstract: 〈 i 〉 Background: 〈 /i 〉 It has been reported that nasal allergy influences the lower airway inflammation and functions. We elucidated whether nasal allergy would contribute to lower airway inflammation and functions. 〈 i 〉 Methods: 〈 /i 〉 266 subjects aged 21–39 years were interviewed with special emphasis on history of asthma and nasal allergies (perennial allergic rhinitis (PAR) and seasonal allergic rhinitis (Japanese cedar pollinosis; PO)). Symptomatic subject was defined when nasal symptoms were present during a 3-week study period. Pulmonary function, provocative concentration of methacholine causing a 20% fall in forced expiratory volume in 1 s (PC 〈 sub 〉 20 〈 /sub 〉 ), capsaicin cough threshold defined as capsaicin concentration eliciting 5 or more coughs (C5) and eosinophil percentage in hypertonic saline-induced sputum were measured. 〈 i 〉 Results: 〈 /i 〉 Based on the interview, 232 subjects without asthma were divided into symptomatic (n = 25) and asymptomatic (n = 22) PAR, PO on-season (n = 15) and off-season (n = 36), and non-nasal allergy subjects (control) (n = 134). Sputum eosinophils were significantly greater in symptomatic PAR than another four groups (p 〈 0.01). FEV 〈 sub 〉 1 〈 /sub 〉 /FVC ratio was significantly lower in PAR than control (p 〈 0.05). Maximum mean expiratory flow was lower in PAR than control (asymptomatic: p 〈 0.05, symptomatic: p = 0.06). C5 was not different among groups. PAR tended to have a lower PC 〈 sub 〉 20 〈 /sub 〉 compared to control (symptomatic: p = 0.078; asymptomatic: p = 0.086). 〈 i 〉 Conclusions: 〈 /i 〉 These results suggest that eosinophilic inflammation occurred in symptomatic period of PAR may contribute to development of lower airway remodeling and bronchial hyperresponsiveness. Reversely, PO may not be associated with lower airway eosinophilic inflammation or abnormal bronchial functions. Nasal allergy dose not influence the cough reflex sensitivity.
    Type of Medium: Online Resource
    ISSN: 1018-2438 , 1423-0097
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2006
    detail.hit.zdb_id: 1482722-0
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  • 6
    Online Resource
    Online Resource
    S. Karger AG ; 2010
    In:  Acta Cytologica Vol. 54, No. 5 ( 2010), p. 695-700
    In: Acta Cytologica, S. Karger AG, Vol. 54, No. 5 ( 2010), p. 695-700
    Type of Medium: Online Resource
    ISSN: 0001-5547 , 1938-2650
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2010
    detail.hit.zdb_id: 2256676-4
    SSG: 12
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  • 7
    In: Respiration, S. Karger AG, Vol. 71, No. 5 ( 2004), p. 505-510
    Abstract: 〈 i 〉 Background: 〈 /i 〉 Although Clara cell secretory protein (CC-10) has been ascribed an anti-inflammatory role in lung diseases, its precise role remains unclear. 〈 i 〉 Objective: 〈 /i 〉 To further our understanding of the role of CC-10 in inflammatory lung diseases, CC-10 protein levels were measured. 〈 i 〉 Methods: 〈 /i 〉 Sera or bronchoalveolar lavage (BAL) fluids were collected from patients with different inflammatory lung diseases including bronchial asthma, chronic obstructive lung disease (COPD), sarcoidosis, idiopathic interstitial pneumonia (IIP), chronic eosinophilic pneumonia (CEP), pneumonia and lung cancer. Serum CC-10 concentrations were measured by enzyme-linked immunosorbent assay using urinary protein-1 antibody. Then, the relationships between CC-10 concentrations and lung diseases were investigated. Immunohistochemistry was performed using lung biopsy samples. 〈 i 〉 Results: 〈 /i 〉 Increased serum CC-10 levels were recognized in IIP patients, while CC-10 levels were decreased in bronchial asthma patients and CEP patients. Immunohistochemistry revealed an aberrant expression in areas of fibrosis in IIP patients. Serum CC-10 concentrations were not associated with severity among IIP, COPD, and sarcoidosis. In contrast, serum CC-10 concentrations were correlated with FEV 〈 sub 〉 1 〈 /sub 〉 /FVC in bronchial asthma patients. 〈 i 〉 Conclusions: 〈 /i 〉 Although the number of patients was quite limited, these data provide new insights into the role of CC-10 in lung diseases, and the possibility that the CC-10 concentration in serum could be a new marker indicating the severity of bronchial asthma.
    Type of Medium: Online Resource
    ISSN: 0025-7931 , 1423-0356
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2004
    detail.hit.zdb_id: 1464419-8
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  • 8
    In: Oncology, S. Karger AG, Vol. 66, No. 3 ( 2004), p. 244-252
    Abstract: 〈 i 〉 Objectives: 〈 /i 〉 We have previously reported that an antioxidant, auraptene (AUR), isolated from citrus fruit effectively inhibits chemically induced carcinogenesis in digestive tracts, such as the oral cavity, esophagus and large bowel. In this study, we investigated the modifying effects of dietary supplementation with AUR on N,N-diethylnitrosamine (DEN)-initiated hepatocarcinogenesis in male F344 rats in two different experiments to determine whether the compound exerts a cancer-chemopreventive action in other organs. 〈 i 〉 Methods: 〈 /i 〉 In the first experiment, animals were fed diets containing AUR at dose levels of 100 and 500 ppm for 7 weeks 1 week before, during, and 1 week after the start of liver carcinogenesis induced by DEN (40 ppm in drinking water for 5 weeks) to predict the modulatory effect on hepatocarcinogenesis. After 7 weeks, the numbers of hepatocellular enzyme-altered foci (EAF; cm 〈 sup 〉 2 〈 /sup 〉 ) which stained positive for the placental form of glutathione 〈 i 〉 S 〈 /i 〉 -transferase (GST-P) and transforming growth factor (TGF)-α were determined on immunohistochemically stained sections. In the second experiment conducted to confirm the findings, animals subjected to DEN treatment were fed AUR-containing diets (100 and 500 ppm) during either the initiation stage (‘initiation’ feeding for 7 weeks) or post-initiation phase (‘post-initiation’ feeding for 25 weeks) of DEN-induced hepatocarcinogenesis. 〈 i 〉 Results: 〈 /i 〉 In the first experiment, feeding with AUR at both doses during DEN exposure decreased the mean numbers of GST-P-positive and TGF-α-positive EAF/cm 〈 sup 〉 2 〈 /sup 〉 , and the reduction in the number of TGF-α-positive EAF by feeding 500 ppm AUR was statistically significant (p 〈 0.005). In the second experiment, the ‘initiation’ feeding with 500 ppm AUR significantly inhibited the incidence (33 vs. 83%, p = 0.000511) and multiplicity (0.67 ± 1.09 vs. 1.96 ± 1.85, p 〈 0.005) of liver cell carcinoma. Also, the ‘post-initiation’ feeding with AUR at both doses significantly reduced the development of hepatocellular carcinoma (100 ppm: incidence, 15%, p = 0.000006; multiplicity: 0.25 ± 0.64, p 〈 0.001; 500 ppm: incidence, 11%, p = 0.000002; multiplicity, 0.26 ± 0.81, p 〈 0.001). In addition, AUR feeding reduced cell proliferation and the apoptotic index in liver cell neoplasms. 〈 i 〉 Conclusions: 〈 /i 〉 The results suggest that the citrus antioxidant AUR is a potential chemopreventive agent against DEN-induced hepatocarcinogenesis in rats.
    Type of Medium: Online Resource
    ISSN: 0030-2414 , 1423-0232
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2004
    detail.hit.zdb_id: 1483096-6
    detail.hit.zdb_id: 250101-6
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  • 9
    In: Neuropsychobiology, S. Karger AG, Vol. 35, No. 2 ( 1997), p. 91-94
    Type of Medium: Online Resource
    ISSN: 0302-282X , 1423-0224
    Language: English
    Publisher: S. Karger AG
    Publication Date: 1997
    detail.hit.zdb_id: 1483094-2
    SSG: 5,2
    SSG: 15,3
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  • 10
    In: Nephron, S. Karger AG, Vol. 142, No. 3 ( 2019), p. 208-215
    Abstract: 〈 b 〉 〈 i 〉 Background: 〈 /i 〉 〈 /b 〉 Screening for hematuria is essential during health checkups in the general population. However, urine examinations in patients with cancer tend to be overlooked. This study attempted to demonstrate the novel utility of urinalysis in the assessment of the prognosis of non-Hodgkin lymphoma (NHL). 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 A longitudinal, retrospective cohort study was conducted to examine the association between hematuria and mortality in 294 patients with NHL. Urinalysis was performed using a dipstick test. A multivariate, logistic regression model was constructed to evaluate factors associated with the presence of hematuria. Statistical association between hematuria and the time to all-cause mortality was analyzed using Kaplan-Meier analysis, followed by multivariate proportional hazards regression analysis adjusted for covariates that might be related to mortality. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 The prevalence of hematuria alone and in combination with proteinuria was 11.6 and 5.1%, respectively. C-reactive protein was a significant factor associated with the presence of hematuria (OR [95% CI] 1.17 [1.03–1.34] , 〈 i 〉 p 〈 /i 〉 = 0.0194). The cumulative mortality was significantly higher in patients with hematuria alone (51.1%), proteinuria alone (47.1%), and both (66.7%), than in those with neither (24.3%). Moreover, the presence of hematuria alone was significantly associated with all-cause mortality (hazard ratio [95% CI] 1.78 [1.10–3.50] , 〈 i 〉 p 〈 /i 〉 = 0.0455), and patients with concomitant proteinuria were at the highest risk (4.01 [1.71–8.33], 〈 i 〉 p 〈 /i 〉 = 0.0001). 〈 b 〉 〈 i 〉 Conclusions: 〈 /i 〉 〈 /b 〉 In patients with hematuric NHL, systemic inflammation is likely to develop to such a great extent that kidney damage occurs. Therefore, the presence of hematuria, alone or especially in combination with proteinuria, predicts a poor prognosis of NHL.
    Type of Medium: Online Resource
    ISSN: 1660-8151 , 2235-3186
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2019
    detail.hit.zdb_id: 2810853-X
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