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  • Wiley  (25)
  • Pharmacy  (25)
  • 1
    In: Alimentary Pharmacology & Therapeutics, Wiley, Vol. 18, No. s1 ( 2003-07), p. 14-23
    Abstract: Background : Long‐term evaluation of gastric pathology after H. pylori infection is very important in order to reveal its clinical implications, since debate still exists on the gastric carcinogenesis provoked by H. pylori infection in animal models. Aim : Either to evaluate the long‐term outcome of H. pylori infection or to determine how H. pylori could provoke gastric cancer in the mice model. Methods : Four‐week‐old specific pathogen free C57BL/6 mice ( n  = 115) were infected with SS1, the mouse‐adapted H. pylori strain. After 4, 8, 16, 24, 36, 50 and 80 weeks of bacterial infection, the H. pylori ‐infected mice were sacrificed. Results : After 80 weeks of infection, almost all the H. pylori ‐infected mice developed hyperplastic gastritis, but did not show any evidence of gastric adenoma, dysplasia or carcinoma. PCNA positive cells were most abundant after 50 weeks and tended to decrease thereafter up to 80 weeks, whereas apoptosis began to be noted 8 weeks after H. pylori infection, showing 7–8 apoptotic cells/high power field, and tending to increase as time passed. Normally observed neutral mucin decreased during the experiment, showing the most marked decrease 50 weeks after H. pylori infection. In contrast, acidic mucin was noted from 50 weeks after infection. Conclusion : The SS1‐infected mouse seems to be a suitable animal model for H. pylori ‐related research, and H. pylori itself does not induce gastric cancer in normal wild‐type mouse model following long‐term exposure, which could be explained by the balance that exists between cell proliferation and apoptosis.
    Type of Medium: Online Resource
    ISSN: 0269-2813 , 1365-2036
    Language: English
    Publisher: Wiley
    Publication Date: 2003
    detail.hit.zdb_id: 2003094-0
    SSG: 15,3
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  • 2
    In: Alimentary Pharmacology & Therapeutics, Wiley, Vol. 40, No. 7 ( 2014-10), p. 819-826
    Abstract: The relationship between relative adrenal insufficiency ( RAI ) and chronic liver disease is unclear. Aim To determine the frequency with which RAI is observed in noncritically ill patients at various stages of chronic liver disease, and the correlation between RAI and disease severity and long‐term mortality. Methods In total, 71 non‐critically ill patients with liver cirrhosis ( n  =   54) and chronic hepatitis ( n  =   17) were evaluated prospectively. A short stimulation test (SST) with 250 μg of corticotrophin was performed to detect RAI. RAI was defined as an increase in serum cortisol of 〈 9 μg/dL in patients with a basal total cortisol of 〈 35 μg/dL. Results RAI was observed in only 13 (24.1%) of 54 patients with cirrhosis. Compared to those without RAI , cirrhotic patients with RAI had significantly higher Child‐Turcotte‐Pugh score (10.3 ± 1.7 vs. 7.1 ± 1.8, mean ± s.d., P  〈   0.001) and Model for End‐Stage Liver Disease score (14.5 ± 6.6 vs. 9.4 ± 3.7, P  =   0.017). The cortisol response to corticotropin was negatively correlated with the severity of cirrhosis ( P  〈   0.05). In addition, the mortality rate was higher in cirrhotic patients with RAI (69.2%) than in those without RAI (4.9%; P  〈   0.001) during the follow‐up period of 20.1 ± 13.5 months (range, 5.8–51.1 months). The cumulative 1‐year survival rates in cirrhotic patients with and without RAI were 69.2% and 95.0%, respectively ( P  =   0.05), while the corresponding cumulative 3‐year survival rates were 0% and 95.0% ( P  〈   0.001). Conclusions Relative adrenal insufficiency is more commonly observed in those with severe cirrhosis, and is clearly associated with more advanced liver disease and a shortened long‐term survival. This suggests that relative adrenal insufficiency is an independent prognostic factor in non‐critically ill patients with cirrhosis.
    Type of Medium: Online Resource
    ISSN: 0269-2813 , 1365-2036
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2014
    detail.hit.zdb_id: 2003094-0
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  • 3
    In: Alimentary Pharmacology & Therapeutics, Wiley, Vol. 16, No. s2 ( 2002-04), p. 115-127
    Abstract: Downregulation of TGF‐β receptors is implicated in colon cancer development. Inactivation of either of the two transmembrane serine/threonine kinases, TGF‐β1 types I/II receptors, is now implicated in carcinogenesis, especially gastrointestinal carcinogenesis. Methods: We generated transgenic mice, called pS2–dnRII or ITF–dnRII, of which the dominant negative mutant of the TGF‐β type II receptor was expressed under the control of tissue‐specific promoters, the pS2 promoter for stomach and ITF for intestine. They were either infected with H. pylori (ATCC 43504 strain, CagA + and VacA + ) or administered with azoxymethane to determine the significance of loss of TGF‐β signalling in gastrointestinal carcinogenesis. Results: Gastric adenocarcinoma developed in pS2–dnRII mice, whereas only chronic active gastritis was noted in wild‐type littermates after 36 weeks of H. pylori infection. Mice lacking in TGF‐β signalling specifically in the stomach showed a significantly higher proliferation cell nuclear antigen‐labelling index when infected with H. pylori than wild‐type littermates ( P 〈  0.01). Development of colonic aberrant crypt foci was provoked in mice by intraperitoneal injections of azoxymethane, and ITF–dnRII mice showed significantly higher incidences of ACF and colon cancers than wild‐type littermates. Conclusions: Maintaining normal TGF‐β signalling in the gastrointestinal tract seems to be important either for preventing abnormal mucosal proliferation, or for suppressing or retarding carcinogenesis.
    Type of Medium: Online Resource
    ISSN: 0269-2813 , 1365-2036
    Language: English
    Publisher: Wiley
    Publication Date: 2002
    detail.hit.zdb_id: 2003094-0
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  • 4
    In: British Journal of Pharmacology, Wiley, Vol. 135, No. 5 ( 2002-03), p. 1235-1244
    Type of Medium: Online Resource
    ISSN: 0007-1188
    Language: English
    Publisher: Wiley
    Publication Date: 2002
    detail.hit.zdb_id: 2029728-2
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  • 5
    In: Alimentary Pharmacology & Therapeutics, Wiley, Vol. 18, No. s1 ( 2003-07), p. 24-38
    Abstract: Background : It has been suggested that chronic, persistent, uncontrolled inflammations in the stomach could provide the basic step for the beginning of carcinogenesis. One of the potential clinical applications of rebamipide is the inhibition of the immunoinflammatory response in gastric mucosa imposed by Helicobacter pylori . Aim : To determine the implications of long‐term rebamipide treatment in H. pylori infection, we studied the underlying moleculo‐pathological changes in gastric lesions in mice infected with H. pylori (SS1 strain), following this treatment. Methods : C57BL/6 mice were sacrificed 24 and 50 weeks after H. pylori infection, respectively. Colonization rates of H. pylori , degree of gastric inflammation and other pathological changes including atrophic gastritis and metaplasia, serum levels of IL‐1β, TNF‐α, IFN‐γ and IL‐10, mRNA transcripts of various mouse cytokines and chemokines, and NF‐κB binding activities, and finally the presence of gastric adenocarcinoma were compared between an H. pylori infected group (HP), and an H. pylori infected group administered with long‐term rebamipide‐containing pellet diets (HPR). Results : Serum levels of IL‐1β, IFN‐γ and TNF‐α, the gastric mucosal expression of ICAM‐1, HCAM and MMP, and transcriptional regulation of NF‐κB‐DNA binding were all significantly decreased in the HPR group compared with the HP group. An RNase protection assay showed, in the rebamipide administered group, significantly decreased mRNA levels of apoptosis‐related genes such as caspase‐8, FasL, Fas, TRAIL and various cytokines genes such as IFN‐γ, RANTES, TNF‐α, TNFR p75, IL‐1β. In the experiment designed to provoke gastric cancer through MNU treatment with H. pylori infection, the incidence of gastric carcinoma was not different in either group. However, long‐term administration of rebamipide showed the advantage of decreasing precancerous lesions like chronic atrophic gastritis and showed molecular evidence of attenuation of proliferation. Conclusion : The long‐term administration of rebamipide should be considered in the treatment of H. pylori since it demonstrated molecular and biological advantages like a lessening of gastric inflammation and a possible chemopreventive effect.
    Type of Medium: Online Resource
    ISSN: 0269-2813 , 1365-2036
    Language: English
    Publisher: Wiley
    Publication Date: 2003
    detail.hit.zdb_id: 2003094-0
    SSG: 15,3
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  • 6
    Online Resource
    Online Resource
    Wiley ; 2018
    In:  Clinical and Experimental Pharmacology and Physiology Vol. 45, No. 3 ( 2018-03), p. 269-277
    In: Clinical and Experimental Pharmacology and Physiology, Wiley, Vol. 45, No. 3 ( 2018-03), p. 269-277
    Abstract: Phosphodiesterase‐5 ( PDE ‐5) inhibitors induces vasodilation in several organs by blocking cyclic GMP (guanosine monophosphate) degradation. However, the existence of alternative mechanism of action in case of an impaired nitric oxide ( NO ) system remains controversial. Previous studies suggested that decreased NO bioavailability may result in the downregulation of klotho expression, but the relationship between klotho and NO remains obscure. Therefore, we investigated whether a PDE ‐5 inhibitor could preserve epithelial–mesenchymal transition ( EMT ) and relationship exists between the NO and renal klotho expression. Ten‐week‐old SD rats (N = 24, 200 g, male) were divided (N = 6) into four groups, which received: A LSD , L‐ NAME 1 mg/ mL in drinking water, Udenafil 5 mg/kg subcutaneously and both for 4 weeks. Urine nitrate/nitrite, NGAL (Neutrophil gelatinase‐associated lipocalin), and cGMP were measured using ELISA . Kidney was subjected to evaluate PCNA (proliferative cell nuclear antigen), α‐ SMA (smooth muscle cell antigen), E‐cadherin, and klotho expression. Urine cGMP decreased after treatment of PDE ‐5 inhibitor compared with control due to blocking degradation of cGMP ( P   〈  .05, control vs Udenafil and L‐ NAME with Udenafil groups). Urine NGAL increased after treating of L‐ NAME and attenuated after using PDE ‐5 inhibitor ( P   〈  .05, control vs L‐ NAME and L‐ NAME with Udenafil). PCNA , α‐ SMA , and E‐cadherin ( EMT markers) increased after L‐ NAME treatment and normalized after using PDE ‐5 inhibitor. Klotho expression showed trend to increase in the L‐ NAME with PDE ‐5 inhibitor group compared with the L‐ NAME group, however, eNOS expression did not change after treatment of L‐ NAME or PDE ‐5 inhibitor compared with control. PDE ‐5 inhibitor alleviates EMT in the kidney via klotho modulation independent of the NO system.
    Type of Medium: Online Resource
    ISSN: 0305-1870 , 1440-1681
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2018
    detail.hit.zdb_id: 2020033-X
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  • 7
    In: British Journal of Pharmacology, Wiley, Vol. 130, No. 3 ( 2000-06), p. 581-586
    Type of Medium: Online Resource
    ISSN: 0007-1188
    Language: English
    Publisher: Wiley
    Publication Date: 2000
    detail.hit.zdb_id: 2029728-2
    SSG: 15,3
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  • 8
    Online Resource
    Online Resource
    Wiley ; 2003
    In:  Alcoholism: Clinical & Experimental Research Vol. 27, No. 2 ( 2003-02), p. 324-335
    In: Alcoholism: Clinical & Experimental Research, Wiley, Vol. 27, No. 2 ( 2003-02), p. 324-335
    Type of Medium: Online Resource
    ISSN: 0145-6008
    Language: English
    Publisher: Wiley
    Publication Date: 2003
    detail.hit.zdb_id: 2046886-6
    detail.hit.zdb_id: 3167872-5
    SSG: 15,3
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  • 9
    In: Alimentary Pharmacology & Therapeutics, Wiley, Vol. 40, No. 11-12 ( 2014-12), p. 1270-1281
    Abstract: Transarterial chemoembolisation ( TACE ) is a standard treatment for unresectable, intermediate stage hepatocellular carcinoma ( HCC ). Survival after TACE , however, can be highly variable, with no suitable biomarker predicting therapeutic outcome. The inflammation‐based index ( IBI ) has previously been shown to independently predict overall survival ( OS ) in all stages of HCC . Aim To explore the prognostic ability of IBI as a predictor of survival after TACE. Methods Baseline staging, biochemical and clinicopathological features including IBI were studied in a derivation set of 64 patients undergoing TACE for intermediate stage HCC . Dynamic changes in IBI before and after TACE were studied as predictors of survival using both a univariate and multivariate Cox regression model and further validated in two independent patient cohorts from Korea ( n  = 76) and Japan ( n  = 577). Results Pre‐treatment IBI predicted for OS in the derivation set ( P  = 0.001). Other univariate predictors of OS included radiological response to TACE ( P   〈  0.001), pre‐TACE CLIP score ( P   〈  0.01), tumour diameter 〉 5 cm ( P  = 0.05) and AFP ≥400 ( P   〈  0.001). Normalisation of IBI post‐TACE was associated with radiological response by mRECIST criteria and improved OS ( P   〈  0.001). Normalisation of IBI remained a significant multivariate predictor of OS in both the derivation and validation sets ( P   〈  0.001). Conclusions Normalisation of IBI after TACE is shown to be an independent predictor of survival and may be integrated into the retreatment criteria for repeat TACE in intermediate stage HCC . IBI and its dynamic changes after treatment are validated as a biomarker allowing the stratification of patients with a significant survival advantage following initial TACE .
    Type of Medium: Online Resource
    ISSN: 0269-2813 , 1365-2036
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2014
    detail.hit.zdb_id: 2003094-0
    SSG: 15,3
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  • 10
    In: The Journal of Clinical Pharmacology, Wiley, Vol. 18, No. 10 ( 1978-10), p. 500-508
    Type of Medium: Online Resource
    ISSN: 0091-2700
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 1978
    detail.hit.zdb_id: 2010253-7
    SSG: 15,3
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