RT Journal Article
SR Electronic
T1 Pharmacological Properties of Y-27632, a Specific Inhibitor of Rho-Associated Kinases
JF Molecular Pharmacology
JO Mol Pharmacol
FD American Society for Pharmacology and Experimental Therapeutics
SP 976
OP 983
VO 57
IS 5
A1 Toshimasa Ishizaki
A1 Masayoshi Uehata
A1 Ichiro Tamechika
A1 Jeongsin Keel
A1 Kimiko Nonomura
A1 Midori Maekawa
A1 Shuh Narumiya
YR 2000
UL http://molpharm.aspetjournals.org/content/57/5/976.abstract
AB Y-27632 [(+)-(R)-trans-4-(1-aminoethyl)-N-(4-pyridyl)cyclohexanecarboxamide dihydrochloride] is widely used as a specific inhibitor of the Rho-associated coiled-coil forming protein serine/threonine kinase (ROCK) family of protein kinases. This study examined the inhibition mechanism and profile of actions of Y-27632 and a related compound, Y-30141 [(+)-(R)-trans- 4-(1-aminoethyl)-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)cyclohexan-ecarboxamide dihydrochloride]. Y-27632 and Y-30141 inhibited the kinase activity of both ROCK-I and ROCK-II in vitro, and this inhibition was reversed by ATP in a competitive manner. This suggests that these compounds inhibit the kinases by binding to the catalytic site. Their affinities for ROCK kinases as determined by Ki values were at least 20 to 30 times higher than those for two other Rho effector kinases, citron kinase and protein kinase PKN. [3H]Y-30141 was taken up by cells in a temperature- and time-dependent and saturable manner, and this uptake was competed with unlabeled Y-27632. No concentrated accumulation was found, suggesting that the uptake is a carrier-mediated facilitated diffusion. Y-27632 abolished stress fibers in Swiss 3T3 cells at 10 μM, but the G1-S phase transition of the cell cycle and cytokinesis were little affected at this concentration. Y-30141 was 10 times more potent than Y-27632 in inhibiting the kinase activity and stress fiber formation, and it caused significant delay in the G1-S transition and inhibition of cytokinesis at 10 μM. The American Society for Pharmacology and Experimental Therapeutics