Protein Information

ID 33
Name ATPase
Synonyms ATP7A; MK; ATPase; Cation transporting ATPase; ATP7A protein; ATPase Cu(2+) transporting alpha polypeptide; Copper pump 1; Copper transporting ATPase 1…

Compound Information

ID 1763
Name scilliroside
CAS

Reference

PubMed Abstract RScore(About this table)
9298532 Schultheiss G, Diener M: Regulation of apical and basolateral K+ conductances in rat colon. . Br J Pharmacol. 1997 Sep;122(1):87-94.
1. Apical administration of an ionophore, nystatin, and basolateral depolarization by K+ were used to investigate the regulation of apical and basolateral electrogenic transport pathways for K+ in the rat proximal and distal colon. 2. Administration of nystatin (100 micrograms ml-1 at the mucosal side), in the presence of Na+ and in the presence of a serosally directed K+ gradient, stimulate a large increase in short-circuit current (ISC) and tissue conductance in both colonic segments. This response was composed of a pump current generated by the Na (+)-K (+)-ATPase and of a current cross a quinine-sensitive basolateral K+ conductance. 3. The pump current, measured as Na (+)-dependent or scilliroside-sensitive current in the absence of a K+ gradient, was significantly greater in the distal than in the proximal colon. The pump current was unaltered by pretreatment of the tissue with forskolin (5 x 10 (-6) mol 1 (-1)). 4. The current across the basolateral K+ conductance, measured as current in the presence of a serosally directed K+ gradient either in the absence of Na+ or in the presence of scilliroside, was increased by the cholinoreceptor agonist, carbachol (5 x 10 (-5) mol 1 (-1)), but inhibited by forskolin (5 x 10 (-6) mol 1 (-1)). 5. Basolateral K+ depolarization induced a negative ISC in both colonic segments, which was inhibited by the K+ channel blocker quinine (10 (-3) mol 1 (-1)) at the mucosal side), but was resistant to tetraethylammonium (5 x 10 (-3) mol 1 (-1) at the mucosal side). This K+ current across an apical K+ conductance was stimulated in both colonic segments by carbachol, whereas forskolin had no effect, although control experiments revealed that forskolin was still able to open an apical Cl- conductance under these conditions. 6. These results demonstrate that an increase in intracellular Ca2+ concentration induced by carbachol causes an increase in the basolateral and the apical K+ conductance, thereby inducing K+ secretion in parallel with an indirect support of Cl- secretion due to the hyperpolarization of the cell membrane. In contrast, the dominating effect of an increase in the intracellular cyclic AMP concentration is inhibition of a basolateral K+ conductance; a mechanism which might contribute to the inhibition of K+ absorption.
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