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Article Publish Status: FREE
Abstract Title:

Endothelium-independent vasodilator effects of nobiletin in rat aorta.

Abstract Source:

J Pharmacol Sci. 2019 May ;140(1):48-53. Epub 2019 Apr 17. PMID: 31088764

Abstract Author(s):

Hisako Kaneda, Rieko Otomo, Noriyasu Sasaki, Toshinori Omi, Tsuyhoshi Sato, Takeharu Kaneda

Article Affiliation:

Hisako Kaneda

Abstract:

Nobiletin is a one of the polymethoxyflavones contained in the peel of citrus fruits, such as Citrus depressa. In this study, the effect of nobiletin-induced relaxation on phenylephrine (PE)-induced contraction of endothelium-denuded rat aorta was investigated. Nobiletin inhibited PE- or KCl-induced contractions in a concentration-dependent manner in endothelium-intact and -denuded aortas. However, this relaxation was stronger in PE-induced contractions than in KCl-induced contractions; moreover, the nobiletin-induced relaxation was significantly increased on PE-induced contraction in endothelium-intact aorta. ODQ significantly inhibited the nobiletin-induced relaxation in endothelium-denuded aorta; however, SQ22536 did not affect the relaxation. In addition, IBMX synergistically enhanced the nobiletin-induced relaxation. Nobiletin increased cGMP levels in aorta. Also, IBMX significantly increased cGMP content in aorta, and ODQ significantly reduced cGMP levels. Nobiletin-induced relaxation was significantly inhibited by the Ca-activated K(BK) channel inhibitor iberiotoxin (IbTX) and the ATP-sensitive K(K) channel inhibitor glybenclamide. Sodium nitroprusside-induced relaxation was suppressed by IbTX, but not by glybenclamide. These results suggest that nobiletin inhibits PE-induced contractions of endothelium-denuded rat aorta by increasing cGMP levels via GC activation. Moreover, the present findings indicate the possibility that nobiletin opened BK channels by a cGMP-related signal, but Kchannels were opened by a cGMP-nonrelated signal in rat aorta.

Study Type : Animal Study
Additional Links
Pharmacological Actions : Vasodilator Agents : CK(347) : AC(74)

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