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Mechanism of Na-K-ATPase Inhibition by PGE2 in Intestinal Epithelial Cells

Overview
Journal Cells
Publisher MDPI
Date 2021 Apr 3
PMID 33805551
Citations 4
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Abstract

The primary means of intestinal absorption of nutrients by villus cells is via Na-dependent nutrient co-transporters located in the brush border membrane (BBM). These secondary active co-transport processes require a favorable transcellular Na gradient that is provided by Na-K-ATPase. In chronic enteritis, malabsorption of essential nutrients is partially due to inhibition of villus Na-K-ATPase activity mediated by specific immune inflammatory mediators that are known to be elevated in the inflamed mucosa. However, how Prostaglandin E2 (PGE2), a specific mediator of nutrient malabsorption in the villus BBM, may mediate the inhibition of Na-K-ATPase is not known. Therefore, this study aimed to determine the effect of PGE2 on Na-K-ATPase in villus cells and define its mechanism of action. In vitro, in IEC-18 cells, PGE2 treatment significantly reduced Na-K-ATPase activity, accompanied by a significant increase in the intracellular levels of cyclic Adenosine Monophosphate (cAMP). The treatment with cAMP analog 8-Bromo-cAMP mimicked the PGE2-mediated effect on Na-K-ATPase activity, while Rp-cAMP (PKA inhibitor) pretreatment reversed the same. The mechanism of inhibition of PGE2 was secondary to a transcriptional reduction in the Na-K-ATPase α1 and β1 subunit genes, which was reversed by the Rp-cAMP pretreatment. Thus, the PGE2-mediated activation of the PKA pathway mediates the transcriptional inhibition of Na-K-ATPase activity in vitro.

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References
1.
Barada K, Okolo C, Field M, Cortas N . Na,K-ATPase in diabetic rat small intestine. Changes at protein and mRNA levels and role of glucagon. J Clin Invest. 1994; 93(6):2725-31. PMC: 294527. DOI: 10.1172/JCI117287. View

2.
Arthur S, Saha P, Sundaram S, Kekuda R, Sundaram U . Regulation of sodium-glutamine cotransport in villus and crypt cells by glucocorticoids during chronic enteritis. Inflamm Bowel Dis. 2012; 18(11):2149-57. DOI: 10.1002/ibd.22924. View

3.
Cimen B, Turkozkan N, Seven I, Unlu A, Karasu C . Impaired Na+,K+-ATPase activity as a mechanism of reactive nitrogen species-induced cytotoxicity in guinea pig liver exposed to lipopolysaccharides. Mol Cell Biochem. 2004; 259(1-2):53-7. DOI: 10.1023/b:mcbi.0000021344.64317.a2. View

4.
Hamberg M, Svensson J, Samuelsson B . Prostaglandin endoperoxides. A new concept concerning the mode of action and release of prostaglandins. Proc Natl Acad Sci U S A. 1974; 71(10):3824-8. PMC: 434276. DOI: 10.1073/pnas.71.10.3824. View

5.
Ligumsky M, Karmeli F, Sharon P, ZOR U, Cohen F, Rachmilewitz D . Enhanced thromboxane A2 and prostacyclin production by cultured rectal mucosa in ulcerative colitis and its inhibition by steroids and sulfasalazine. Gastroenterology. 1981; 81(3):444-9. View