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Heartwood extract of Rhus verniciflua Stokes and its active constituent fisetin attenuate vasoconstriction through calcium-dependent mechanism in rat aorta
Rhus verniciflua Stokes (RVS) exert cardiovascular protective activity by promoting blood circulation, but its active ingredients and underlying mechanism have yet to be identified. This study investigated the vascular effects of RVS, focusing on vasoconstriction and smooth muscle Ca 2+ signaling. R...
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Published in: | Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2016-03, Vol.80 (3), p.493-500 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Rhus verniciflua Stokes (RVS) exert cardiovascular protective activity by promoting blood circulation, but its active ingredients and underlying mechanism have yet to be identified. This study investigated the vascular effects of RVS, focusing on vasoconstriction and smooth muscle Ca
2+
signaling. RVS heartwood extract attenuated contraction of aortic rings induced by the vasoconstrictors serotonin and phenylephrine, and inhibited the Ca
2+
signaling evoked by serotonin in vascular smooth muscle cells. Subsequent activity-guided fractionation identified fisetin as an active constituent exerting a Ca
2+
inhibitory effect. Fisetin could inhibit major Ca
2+
mobilization pathways including extracellular Ca
2+
influx mediated by the L-type voltage-gated Ca
2+
channel, Ca
2+
release from the intracellular store and store-operated Ca
2+
entry. In accordance with Ca
2+
inhibitory effect, fisetin attenuated vasoconstriction by serotonin and phenylephrine. These results suggest that the anticontractile effect, which is presumably mediated by inhibition of Ca
2+
signaling, may contribute to the improvement of blood circulation by RVS.
Rhus verniciflua Stokes extract and its active constituent fisetin improve blood circulation by inhibiting smooth muscle Ca
2+
signaling and thereby attenuating vasoconstriction. |
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ISSN: | 0916-8451 1347-6947 |
DOI: | 10.1080/09168451.2015.1107464 |