European Journal of Pharmacology 2000-10-06

Inhibitors of tyrosine phosphatases block angiotensin II inhibition of Na(+) pump.

D R Yingst, J Davis, R Schiebinger, Douglas R. Yingst, Joanne Davis, Rick Schiebinger

Index: Eur. J. Pharmacol. 406(1) , 49-52, (2000)

Full Text: HTML

Abstract

To determine how angiotensin II inhibits the Na(+) pump (Na(+), K(+)-ATPase) in rat zona glomerulosa, we selectively blocked signaling proteins that could be activated by the angiotensin AT(1) receptor and known to affect Na(+) pump activity. Inhibitors of protein kinase C [calphostin C (1 microM); staurosporine (1 microM)], phospholipase A(2) [arachidonyl triflouromethyl ketone (25 microM); quinacrine (75 microM)], diacylgycerol lipase [RHC-80267 (5 microM)], and tyrosine phosphorylation [tyrphostin 47 (100 microM)] had no effect on angiotensin II inhibition of the Na(+) pump. On the other hand, inhibitors of tyrosine phosphatases [phenylarsine oxide (5 microM) and 4-bromotetramisole oxalate (100 microM)] blocked angiotensin II inhibition, where as inhibitors of serine/threonine phosphatases [okadaic acid (1 microM) and microcystin (1.5 microM)] did not. Thus, angiotensin II inhibition of the Na(+) pump may in part be mediated by a tyrosine phosphatase.


Related Compounds

  • (-)-p-Bromotetrami...

Related Articles:

Chemical genetics reveals a complex functional ground state of neural stem cells.

2007-05-01

[Nat. Chem. Biol. 3(5) , 268-273, (2007)]

Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum.

2009-10-01

[Nat. Chem. Biol. 5 , 765-71, (2009)]

Endothelial progenitor cells proliferated via MEK-dependent p42 MAPK signaling pathway.

2015-02-01

[Mol. Cell Biochem. 400(1-2) , 201-6, (2015)]

Inhibition of human alkaline phosphatase isoenzymes by the affinity reagent reactive yellow 13.

1985-01-01

[Enzyme 33(2) , 70-4, (1985)]

Further characterization of serum alkaline phosphatase from male and female beagle dogs.

1989-01-01

[Enzyme 42(1) , 1-7, (1989)]

More Articles...