Biochemical Journal 1997-04-15

Diadenosine polyphosphate-stimulated gluconeogenesis in isolated rat proximal tubules.

M Edgecombe, H S Craddock, D C Smith, A G McLennan, M J Fisher

Index: Biochem. J. 323 , 451-456, (1997)

Full Text: HTML

Abstract

Diadenosine polyphosphates released into the extracellular environment influence a variety of metabolic and other cellular activities in a wide range of target tissues. Here we have studied the impact of these novel nucleotides on gluconeogenesis in isolated rat proximal tubules. Gluconeogenesis was stimulated following exposure of isolated proximal tubules to a range of adenine-containing nucleotides including ADP, ATP, Ap3A, Ap4A, Ap5A and Ap6A. The concentration-dependence of ATP-, Ap3A- and Ap4A-mediated stimulation of gluconeogenesis was similar and was consistent with a role for these agents in the physiological control of renal metabolism. Nucleotide-stimulated gluconeogenesis was diminished in the presence of agents that interfere with phospholipase C activation or intracellular Ca2+ metabolism, indicative of a role for polyphosphoinositide-mediated Ca2+ mobilization in the mechanism of action of ATP, Ap3A and Ap4A. The characteristics of binding of [2-3H]Ap4A to renal plasma-membrane preparations suggest that Ap4A mediates its effects on proximal tubule gluconeogenesis via interaction with P2y-like purinoceptor(s) also recognized by extracellular ATP.


Related Compounds

Related Articles:

Adenine dinucleotides: a novel class of signalling molecules.

1996-12-01

[J. Auton. Pharmacol. 16 , 325-328, (1996)]

Selectivity of diadenosine polyphosphates for rat P2X receptor subunits.

1999-02-12

[Eur. J. Pharmacol. 367 , 19-123, (1999)]

Diadenosine polyphosphates in insulin-secreting cells: interaction with specific receptors and degradation.

1998-11-01

[Diabetes 47 , 1727-1734, (1998)]

P1,P4-diadenosine 5' tetraphosphate induces nitric oxide release from bovine aortic endothelial cells.

1998-05-15

[FEBS Lett. 427 , 320, (1998)]

Diadenosine polyphosphates inhibit adenosine kinase activity but decrease levels of endogenous adenosine in rat brain.

1997-07-30

[Eur. J. Pharmacol. 322 , 5-42, (1997)]

More Articles...