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Taurocholate Potentiates Ethanol-Induced NF-κB Activation and Inhibits Caspase-3 Activity in Cultured Rat Gastric Mucosal Cells
被引:9
作者:
Mustonen, Harri
[1
]
Puolakkainen, Pauli
[1
]
Kemppainen, Esko
[1
]
Kiviluoto, Tuula
[1
]
Kivilaakso, Eero
[1
]
机构:
[1] Univ Helsinki, Dept Surg, Cent Hosp, HUS, Helsinki 00029, Finland
关键词:
NF-kappa B;
Acetylsalicylic acid;
Taurocholate gastric mucosa;
Apoptosis;
GAP-JUNCTION CLOSURE;
ACETYLSALICYLIC-ACID;
APOPTOSIS;
PROTEINS;
THERAPY;
BARRIER;
BINDING;
D O I:
10.1007/s10620-008-0533-2
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
We have previously shown that ethanol (EtOH) induces protective NF-kappa B activation in gastric surface epithelial cells. This study investigates the defense systems in rat gastric mucosal cells (RGM-1) exposed simultaneously to EtOH and taurocholate (TC) or acetylsalicylic acid (ASA). Simultaneous exposure to ASA and EtOH increased EtOH-induced caspase-3 activity and decreased cell viability, indicating synergetic damaging action. Simultaneous exposure to TC (5 mM) with EtOH (5%) increased EtOH-induced NF-kappa B activation, opposing EtOH-induced decrease in cell membrane integrity and in cell viability as shown by decreasing RelA expression with siRNA technique. Low doses of TC decreased the EtOH (5%) induced caspase-3 activity independently from NF-kappa B pathway and inhibited EtOH-induced decrease in caspase-3 precursor protein levels, also indicating the inhibition of caspase-3 pathway. The TC (5 mM)-induced protection in EtOH exposed tissues seems to have two distinct pathways, inhibition of apoptosis and enhancement of NF-kappa B signaling.
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页码:928 / 936
页数:9
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