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(Hypertension. 2005;45:974.)
© 2005 American Heart Association, Inc.

Original Articles

Involvement of RhoA/Rho Kinase Pathway in Myogenic Tone in the Rabbit Facial Vein

Caroline Dubroca; Dong You; Bernard I. Lévy; Laurent Loufrani; Daniel Henrion

From INSERM Unit 541 (C.D., D.Y., B.I.L.), Paris, France; CNRS-UMR 6188 (L.L., D.H.), Université d’Angers, Angers, France.

Correspondence to Daniel Henrion, CNRS-UMR 6188, Faculté de Medecine, 49045 Angers, France. E-mail daniel.henrion{at}med.univ-angers.fr

Myogenic tone (MT), a fundamental stretch-sensitive vasoconstrictor property of resistance arteries and veins, is a key determinant of local blood flow regulation. We evaluated the pathways involved in MT development. The role of the RhoA/Rho kinase, p38 MAP kinase, and HSP27 in MT was investigated in the rabbit facial vein (RFV), previously shown to possess MT at a pressure level equivalent to 20 mm Hg. Venous MT is poorly understood, although venous diseases affect a large proportion of the population. Stretched RFV are characterized by a temperature-sensitive MT, which is normal at 39°C but fails to develop at 33°C. This allows for the discrimination of the pathways involved in MT from the multiple pathways activated by stretch. Isolated RFV segments were mounted in organ baths and stretched. Temperature was then set at 33°C or 39°C. MT was associated to the translocation of RhoA to the plasma membrane and the Rho kinase inhibitor Y27632 decreased stretch-induced MT by 93.1±4.9%. MT was also associated to an increase in p38 (131.0±12.5% at 39°C versus 100% at 33°C) and HSP27 phosphorylation (196.1±13.3% versus 100%), and the p38 MAP kinase inhibitor SB203580 decreased MT by 36.5±8.1%. (39°C, compared with RFV stretched at 33°C). Finally, phosphorylation of p38 was blocked by Y27632 and HSP27 phosphorylation was inhibited by SB203580 and Y27632. Thus, MT and the associated p38 and HSP27 phosphorylation seem to depend on RhoA/Rho kinase activation in stretch RFV.

Key Words: signal transduction • kinase • heat shock proteins

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