Effect of prostanoids on human intestinal Na-K-ATPase activity
Abstract:
To elucidate whether prostanoids affect the activity of human intestinal Na-K-ATPase (an enzyme that has an important role in intestinal sodium and water absorption), basal human jejunal and colonic Na-K-ATPase activities were measured. In normal subjects, the mean (+/- SE) activities were 2.30 +/- 0.20 (n = 18) and 2.06 +/- 0.27 (n = 12) mumol/h . mg protein, respectively. Prostaglandin (PG) E2 (1.3 microM) induced significant inhibition of both the jejunal and the colonic enzyme activities: 82 +/- 5 and 50 +/- 8% inhibition, respectively. The inhibition of the colonic enzyme activity was apparent after 5 min of incubation and was linear in the first 20 min; it correlated with the amount of enzyme protein. PGD2, 6-keto-PGF1 alpha and thromboxane B2 did not affect either the jejunal or colonic Na-K-ATPase activities. These results indicate that PGE2 inhibits intestinal Na-K-ATPase activity. This inhibition may increase intestinal net fluid accumulation and thus may contribute to the diarrhea induced by several prostanoids.
Related Concept Videos
ATP Driven Pumps I: An Overview
There are four main types of ATP-driven pumps - P-type, V-type, F-type, and ABC transporter. All these pumps are of varying complexities and are...
Adrenergic Receptors: ɑ Subtype
Adrenaline ≥ Noradrenaline >> Isoprenaline
α-adrenoceptors are further divided into α1 and α2-adrenoceptors.
α1-Adrenoceptors: These receptors are located postsynaptically on the effector organs and cause constriction of smooth muscle mediated by activation of phospholipase C—inositol-1,4,5-trisphosphate...
Adrenergic Receptors: β Subtype
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors have equal affinities for...
Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents
Non-steroidal anti-inflammatory drugs (NSAIDs) can induce peptic ulcers by inhibiting cyclooxygenase, decreasing...
Drugs Affecting GI Tract Motility: Dopamine Receptor Antagonists
Drugs Affecting GI Tract Motility: Serotonin Receptor Agonists


