Title : Rilmenidine improves hepatic steatosis through p38-dependent pathway to higher the expression of farnesoid X receptor.

Pub. Date : 2012 Jan

PMID : 21947253






6 Functional Relationships(s)
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1 It has been reported that activation of imidazoline I-1 receptor by rilmenidine increases the expression of FXR in human hepatoma cell line, Hep G2 cell, to regulate the target genes relating to lipid metabolism; activation of FXR by rilmenidine exerts an antihyperlipidemic action. Rilmenidine nuclear receptor subfamily 1 group H member 4 Homo sapiens
2 It has been reported that activation of imidazoline I-1 receptor by rilmenidine increases the expression of FXR in human hepatoma cell line, Hep G2 cell, to regulate the target genes relating to lipid metabolism; activation of FXR by rilmenidine exerts an antihyperlipidemic action. Rilmenidine nuclear receptor subfamily 1 group H member 4 Homo sapiens
3 It has been reported that activation of imidazoline I-1 receptor by rilmenidine increases the expression of FXR in human hepatoma cell line, Hep G2 cell, to regulate the target genes relating to lipid metabolism; activation of FXR by rilmenidine exerts an antihyperlipidemic action. Rilmenidine nuclear receptor subfamily 1 group H member 4 Homo sapiens
4 It has been reported that activation of imidazoline I-1 receptor by rilmenidine increases the expression of FXR in human hepatoma cell line, Hep G2 cell, to regulate the target genes relating to lipid metabolism; activation of FXR by rilmenidine exerts an antihyperlipidemic action. Rilmenidine nuclear receptor subfamily 1 group H member 4 Homo sapiens
5 Otherwise, rilmenidine increased the phosphorylation of p38 to increase the expression of FXR. Rilmenidine nuclear receptor subfamily 1 group H member 4 Homo sapiens
6 In conclusion, we suggest that rilmenidine activates I-1 receptor to increase intracellular calcium ions that may enhance the phosphorylation of p38 to higher the expression of FXR for improvement of hepatic steatosis in both animals and cells. Rilmenidine nuclear receptor subfamily 1 group H member 4 Homo sapiens