Flavone Attenuates Vascular Contractions by Inhibiting RhoA/Rho Kinase Pathway

• Published in: The Korean journal of physiology & pharmacology Vol. 13; no. 3; pp. 201 - 207
• Main Authors: Baek, In-Ji, Jeon, Su-Bun, Song, Min-Ji, Yang, Enyue, Sohn, Uy-Dong, Kim, In-Kyeom
• Format: Journal Article
• Language: Korean
• Published: 대한생리학회-대한약리학회 01.01.2009; The Korean Journal of Physiology & Pharmacology Editorial Office
• Subjects: CPI-17; Rho kinase; Vasorelaxation; Flavone; RhoA; MYPT1
• ISSN: 1226-4512; 2093-3827

Our previous study demonstrated that flavone inhibits vascular contractions by decreasing the phosphorylation levelof the myosin phosphatase target subunit (MYPT1). In the present study, we hypothesized that flavone attenuates vascular contractions through the inhibition of the RhoA/Rho kinase pathway. Rat aortic rings were denuded of endothelium, mounted in organ baths, and contracted with either 30 nM U46619 (a thromboxane A2 analogue) or 8.0 mM NaF 30 min after pretreatment with either flavone (100 or 300 $({\mu}M$) or vehicle. We determined the phosphorylation level of the myosin light chain ($MLC_{20}$), the myosin phophatase targeting subunit 1 (MYPT1) and the protein kinase C-potentiated inhibitory protein for heterotrimeric myosin light chain phophatase of 17-kDa (CPI17) by means of Western blot analysis. Flavone inhibited, not only vascular contractions induced by these contractors, but also the levels of $MLC_{20}$ phosphorylation. Furthermore, flavone inhibited the activation of RhoA which had been induced by either U46619 or NaF. Incubation with flavone attenuated U46619 or NaF-induced phosphorylation of $MYPT1^{Thr855}$ and $CPI17^{Thr38}$, the downstream effectors of Rho-kinase. In regards to the $Ca^{2+}$-free solution, flavone inhibited the phosphorylation of $MYPT1^{Thr855}$ and $CPI17^{Thr38}$, as well as vascular contractions induced by U 46619. These results indicate that flavone attenuates vascular contractions, at least in part, through the inhibition of the RhoA/Rho-kinase pathway.