Abstract

We studied the effect of naloxone--an antagonist of the opioid receptors--on sensitivity of Cl(-)-activated Mg(2+)-ATPase from the plasma membrane fraction of bream brain (Abramis brama L.) to GABAa-ergic substances. Preincubation of the plasma membranes with 1-100 microM naloxone increased the basal Mg(2+)-ATPase activity and suppressed its activation by chloride ions. The same effects were observed in the presence of the agonists of GABAa/benzodiazepine receptors: 0.1-100 microM GABA, 1-500 microM pentobarbital, and 0.1-100 microM phenazepam. Naloxone (10 microM) inhibited the activation of the basal Mg(2+)-ATPase by the studied ligands and regenerated the enzyme sensitivity to Cl-. However, the effect of naloxone was not observed in the presence of high concentrations of pentobarbital (500 microM) and phenazepam (100 microM). The obtained data show that naloxone modulates the activity of Cl(-)-activated Mg(2+)-ATPase from the plasma membranes of bream brain and antagonizes the GABAa receptor ligands.

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