Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1926285 | Archives of Biochemistry and Biophysics | 2009 | 6 Pages |
We have previously demonstrated that adenosine is deaminated to inosine in the isolated basolateral membrane (BLM) of kidney proximal tubules. This work investigates the possible effect of inosine on proximal tubule Na+-ATPase activity. Inosine reduced Na+-ATPase activity by 70%. This effect of inosine was completely attenuated by 10−8 M DPCPX, an A1 receptor-selective antagonist, but it was not affected by either 10−8 M DMPX or 10−7 M MRS1523, A2 and A3 receptor-selective antagonists, respectively. The inhibitory effect of inosine was blocked by: (1) 10−6 M GDPβS, a trimeric G protein inhibitor; (2) 1 μg/ml pertussis toxin, a Gi protein inhibitor; (3) 10−6 M forskolin, an adenylyl cyclase activator; (4) 10−9 M cholera toxin, a Gs protein activator; (5) 10−6 M cAMP. Our results demonstrate that the inhibitory effect of inosine on the sodium pump is mediated by the A1 receptor/Gi/cAMP pathway.