Inhibition of rat brain Na+-K+-ATPase by triterpene glycosides from holothurians

Toxicon. 1989;27(8):927-36. doi: 10.1016/0041-0101(89)90104-9.

Abstract

The effect of triterpene glycosides from holothurians on Na+-K+-ATPase of rat brain was investigated. The marine glycosides are irreversible inhibitors of the enzyme with an average I50 value of 10(-4) M. ATP had a low protective effect against inhibition. The inhibitory effect was increased by preincubation with MgCl2. There was alteration of the activation curve of Na+-K+-ATPase by NaCl and KCl in the presence of glycosides. Triterpene glycosides inhibited the K+-phosphatase activity, but to a smaller degree than the ATPase activity. Na+-K+-ATPase of pig kidney was less sensitive to the marine triterpene glycosides than the brain enzyme. The marine glycosides did not alter the specific binding of [3H]-ouabain to the Na+-K+-ATPase.

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Animals
  • Brain / enzymology*
  • Glycosides / pharmacology*
  • Magnesium / pharmacology
  • Magnesium Chloride
  • Ouabain / pharmacology
  • Potassium / pharmacology
  • Rats
  • Sea Cucumbers
  • Sodium / pharmacology
  • Sodium-Potassium-Exchanging ATPase / antagonists & inhibitors*
  • Structure-Activity Relationship
  • Triterpenes / pharmacology*

Substances

  • Glycosides
  • Triterpenes
  • Magnesium Chloride
  • Ouabain
  • Adenosine Triphosphate
  • Sodium
  • Sodium-Potassium-Exchanging ATPase
  • Magnesium
  • Potassium