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.
引用
收藏
页码:928 / 936
页数:9
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