A role for Rho kinase in vascular contraction evoked by sodium fluoride |
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Authors: | Jeon Su Bun Jin Fanxue Kim Jee In Kim Sang-Hyun Suk Kyoungho Chae Shung Chull Jun Jae Eun Park Wee Hyun Kim In Kyeom |
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Institution: | Department of Pharmacology, Kyungpook National University School of Medicine, Daegu 700-422, Republic of Korea. |
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Abstract: | Agonist and depolarization-induced vascular smooth muscle contractions involve the activation of Rho-kinase pathway. However, there are no reports addressing the question whether this pathway is involved in NaF-induced vascular contractions. We hypothesized that Rho-kinase plays a role in vascular contraction evoked by sodium fluoride in rat aortae. In both physiological salt solution and calcium-free solution with 2 mM EGTA, cumulative addition of NaF increased vascular tension in concentration-dependent manners. Effects of Rho-kinase inhibitor (Y27632) on phosphorylation of myosin light chain (MLC20) and myosin targeting subunit (MYPT1(Thr696)) of myosin light chain phosphatase as well as NaF-induced contractions were determined using isolated tissue and the Western blot experiments. Y27632 inhibited NaF-induced contractions in a concentration-dependent manner. NaF increased phosphorylation of MLC20 and MYPT1(Thr696), which were also inhibited by Y27632. However, MLCK inhibitor (ML-7) or PKC inhibitor (Ro31-8220) did not inhibit the NaF-induced contraction. These results indicate that activation of Rho-kinase and the subsequent phosphorylation of MYPT1(Thr696) play important roles in NaF-induced contraction of rat aortae. |
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Keywords: | Fluoride Contraction Rho kinase Y27632 |
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