Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Subscribe

Sci. Signal., 22 January 2008
Vol. 1, Issue 3, p. ec23
[DOI: 10.1126/stke.13ec23]

EDITORS' CHOICE

Hypertension Pass on the Salt

John F. Foley

Science Signaling, AAAS, Washington, DC 20005, USA

Salt is well known to promote hypertension, but the mechanisms involved in regulating the tone of arterial smooth muscle are poorly characterized. This is particularly true with regard to our understanding of whether similar or distinct mechanisms are responsible for regulating both basal blood pressure and salt-induced hypertension. Phosphorylation of myosin light chain (MLC) is critical for the vascular constriction that is associated with hypertension. Many receptors promote the phosphorylation of MLC either by stimulating MLC kinase, through the activation of heterotrimeric GTP-binding proteins (G proteins) of the Gq and G11 families, or by inhibiting, through G12 and G13 G proteins, the phosphatase that returns MLC to its inactive form. Wirth et al. produced mice that could be induced by treatment with tamoxifen to lack both Gq and G11 (Gq-G11 KO) or both G12 and G13 (G12-G13 KO) in smooth muscle cells. Treatment with tamoxifen caused an increase in blood pressure in all mice, but whereas the blood pressure of wild-type and G12-G13 KO mice soon returned to basal levels, that of Gq-G11 KO mice became 10 to 15% lower than normal, implicating Gq and G11 in the regulation of basal blood pressure. Treatment of wild-type mice with a salt preparation increased their blood pressure, but Gq-G11 KO and G12-G13 KO mice were unaffected, showing that both sets of G proteins mediate salt-induced hypertension. Mice deficient in LARG, an effector of G12 and G13 found in smooth muscle cells that mediates the inhibition of myosin phosphatase, responded to salt treatment similarly to G12-G13 KO mice. As Schoner discusses in commentary, this study makes possible the development of therapies that could interfere with salt-induced hypertension while leaving basal blood pressure regulation intact.

A. Wirth, Z. Benyó, M. Lukasova, B. Leutgeb, N. Wettschureck, S. Gorbey, P. Orsy, B. Horváth, C. Maser-Gluth, E. Greiner, B. Lemmer, G. Schütz, J. S. Gutkind, S. Offermanns, G12-G13-LARG-mediated signaling in vascular smooth muscle is required for salt-induced hypertension. Nat. Med. 14, 64-68 (2008). [PubMed]

W. Schoner, Salt abuse: The path to hypertension. Nat. Med. 14, 16-17 (2008). [PubMed]

Citation: J. F. Foley, Pass on the Salt. Sci. Signal. 1, ec23 (2008).



To Advertise     Find Products


Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882