Biochimica et biophysica acta · 1997
Effect of adenosine on the ouabain-insensitive Na+-ATPase activity from basolateral membrane of the proximal tubule.
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Caruso-Neves C, Francisco-Pedro L G, Souza L P, Chagas C, Lopes A G
Аннотация
The regulation of the furosemide-sensitive Na+-ATPase activity and ouabain-sensitive (Na+ + K+)ATPase activities from proximal tubules by adenosine was investigated. When the concentration of adenosine was increased the furosemide-sensitive ATPase activity decreased with maximal inhibition at 10(-8) M (56% of inhibition). However, the (Na+ + K+)ATPase activity was not affected by adenosine. Theophylline, an antagonist of P1 adenosine receptor, completely reversed the effect of adenosine on the furosemide-sensitive ATPase activity in a dose-response manner. The adenosine effect was mimicked by N6-cyclohexyladenosine (CHA), an agonist for A1 adenosine receptor. 5'-N-ethylcarboxamideadenosine (NECA), an agonist for A2 adenosine receptor, did not affect the furosemide-sensitive ATPase activity. When adenosine was used in the presence of 1 microg ml(-1) pertussis toxin, a Gi protein inhibitor, no change in the furosemide-sensitive ATPase activity was observed. The addition of 1 nM cholera toxin increased the Na+-ATPase activity by 60%. Adenosine decreased the cholera toxin stimulated Na+-ATPase in 42%, similar to the effect observed in the absence of cholera toxin. Dibutyryl-cAMP reversed the effect of adenosine in a dose dependent manner while the protein kinase A peptide inhibitor mimicked it. These data are compatible with a modulatory effect of adenosine on the Na+-ATPase activity via A1 subtype receptor.
Предметные рубрики MeSH
AdenosineAdenosine TriphosphatasesAdenosine-5'-(N-ethylcarboxamide)AnimalsBucladesineCation Transport ProteinsCell MembraneCholera ToxinCyclic AMP-Dependent Protein KinasesEnzyme InhibitorsFurosemideKidney CortexKidney Tubules, ProximalKineticsOuabainPurinergic P1 Receptor AgonistsPurinergic P1 Receptor AntagonistsSodium-Potassium-Exchanging ATPaseSwineTheophylline