Polaprezinc down-regulates proinflammatory cytokine-induced nuclear factor-kappaB activiation and interleukin-8 expression in gastric epithelial cells.
Polaprezinc down-regulates proinflammatory cytokine-induced nuclear factor-kappaB activiation and interleukin-8 expression in gastric epithelial cells.
复制标题
Polaprezinc 下调胃上皮细胞中促炎细胞因子诱导的核因子 kappaB 激活和白细胞介素 8 表达。
DOI:
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发表时间:
1999
影响因子:
3.5
通讯作者:
A. Terano
中科院分区:
文献类型:
--
作者:
T. Shimada;N. Watanabe;Y. Ohtsuka;M. Endoh;K. Kojima;H. Hiraishi;A. Terano
Gastric epithelial chemokine response is a primary factor in the induction of gastric inflammation associated with Helicobacter pylori infection. Because sustained inflammation is a risk for gastric mucosal damage, agents that down-regulate inflammatory responses may be of therapeutic significance. We examined the effect of polaprezinc, a potent antiulcer agent, on proinflammatory cytokine-induced interleukin (IL)-8 expression in gastric epithelial cells. Because IL-8 expression is regulated by the transcription factor nuclear factor-kappaB (NF-kappaB), we also examined the effect of polaprezinc on NF-kappaB activity. MKN28 cells were used as a model of gastric epithelial cells. Secreted IL-8 was quantified by IL-8 specific enzyme-linked immunosorbent assay, and IL-8 mRNA expression was examined by Northern blot analysis. NF-kappaB activity was analyzed by electrophoretic mobility shift assay. Western blot analysis with anti-phospho-IkappaB-alpha antibody was performed to assess IkappaB-alpha phosphorylation. Polaprezinc-suppressed IL-8 secretion induced by tumor necrosis factor alpha (TNF-alpha) or IL-1beta in a dose-dependent manner. IL-8 mRNA expression also was inhibited by polaprezinc. NF-kappaB activation in response to TNF-alpha, IL-1beta, phorbol ester, and H(2)O(2) was down-regulated by polaprezinc. Western blot analysis showed inhibition of TNF-alpha-induced IkappaB-alpha phosphorylation in the presence of polaprezinc. Collectively, these results suggest that polaprezinc is a novel type of anti-inflammatory agent that down-regulates inflammatory responses of gastric mucosal cells.
影响因子:
29.4
作者:
Keates, S;Hitti, YS;Kelly, CP
通讯作者:
Kelly, CP
影响因子:
1.8
作者:
Atta, Ananta Kumar;Ahn, In-Ho;Cho, Dong-Gyu
通讯作者:
Cho, Dong-Gyu
DOI:
10.1080/07315724.1997.10718706
发表时间:
1997-10-01
影响因子:
3.5
作者:
Connell, P;Young, VM;Hennig, B
通讯作者:
Hennig, B