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Life Sci ; 88(3-4): 194-200, 2011 Jan 17.
Article in English | MEDLINE | ID: mdl-21094173

ABSTRACT

AIMS: We have suggested that an osmotic laxative, magnesium sulphate (MgSO(4)), may act as a cathartic in a very rational manner by increasing the aquaporin 3 (AQP3) expression level and by changing osmotic pressure in the colon. In this study, we examined the mechanism by which MgSO(4) increases the intestinal AQP3 expression level by using the human colon cancer HT-29 cell line. MAIN METHODS: After the addition of MgSO(4) to HT-29 cells, the expression levels of AQP3 mRNA and protein were measured using real-time RT-PCR and western blotting, respectively. The intracellular Mg(2+) concentration, adenylate cyclase (AC) activity and protein kinase A (PKA) activity were also determined. The phosphorylated cAMP response element-binding protein (CREB) expression levels were determined by western blotting. KEY FINDINGS: The AQP3 mRNA expression level started to increase significantly at 1 h after MgSO(4) addition and peaked at 9 h, at a level 3 times as high as the control levels. The AQP3 protein expression level started to increase 6 h after the addition and reached a level almost twice as high as the control levels by hour 12. In the HT-29 cells treated with MgSO(4), there was a 1.4-fold increase in the intracellular Mg(2+) concentration, a 1.5-fold increase in AC activity, a 1.6-fold increase in PKA activity, and a significant increase in phosphorylation of the CREB. SIGNIFICANCE: These results suggest that the AC activation caused by an increase in the intracellular Mg(2+) concentration may trigger CREB phosphorylation through PKA activation and promote AQP3 gene transcription.


Subject(s)
Aquaporin 3/metabolism , Gene Expression Regulation/drug effects , Intestines/drug effects , Laxatives/pharmacology , Magnesium Sulfate/pharmacology , Adenylyl Cyclases/metabolism , Analysis of Variance , Blotting, Western , Cell Line, Tumor , Cyclic AMP Response Element-Binding Protein/metabolism , Cyclic AMP-Dependent Protein Kinases/metabolism , DNA Primers/genetics , Electrophoresis , Humans , Intestinal Mucosa/metabolism , Magnesium/metabolism , Osmotic Pressure , Reverse Transcriptase Polymerase Chain Reaction
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