The vascular dilatation induced by Hydroxysafflor yellow A (HSYA) on rat mesenteric artery through TRPV4-dependent calcium influx in endothelial cells.
Animals
Calcium
/ metabolism
Carthamus tinctorius
/ chemistry
Chalcone
/ analogs & derivatives
Dilatation
/ methods
Endothelial Cells
/ drug effects
Endothelium, Vascular
/ drug effects
Male
Mesenteric Arteries
/ drug effects
NG-Nitroarginine Methyl Ester
/ pharmacology
Nitric Oxide
/ metabolism
Quinones
/ pharmacology
Rats
Rats, Wistar
TRPV Cation Channels
/ metabolism
Vasodilation
/ drug effects
Vasodilator Agents
/ pharmacology
Calcium influx
Endothelial cells
HSYA
Protein kinase A
PubChem CID: 6443665
TRPV4
Vascular dilatation
Journal
Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310
Informations de publication
Date de publication:
28 Jun 2020
28 Jun 2020
Historique:
received:
14
01
2020
revised:
20
03
2020
accepted:
21
03
2020
pubmed:
3
4
2020
medline:
28
1
2021
entrez:
3
4
2020
Statut:
ppublish
Résumé
Hydroxysafflor yellow A (HSYA) is the principal constituent of the flowers of Carthamus tinctorius L., a traditional Chinese herbal medicine, which has been used for the treatment of cerebrovascular and cardiovascular diseases due to its property of promoting blood circulation and removing blood stasis. It is dominated in the water extract of Carthamus tinctorius L., which has been used in the clinical treatment for cardiovascular diseases. HSYA exerts a variety of pharmacological efficacy upon the vascular system. However, the underlying mechanisms remain unclear. To investigate the vascular dilatation effect of HSYA on rat mesenteric artery (MA) and its potential mechanism. Adult male Wistar rats were applied to the study. Tension studies were conducted to determine the dilatation activity of HSYA against pre-contracted mesenteric arterial (MA) rings by U 46619 and Phenylephrine (PE). The vascular activities were measured with or without incubation with some selective inhibitors, including L-N(ω)-nitro-L-arginine methyl ester (L-NAME, a nitro oxide synthase inhibitor), HC-067047 (a selective TRPV4 antagonist), BaCl HSYA reversed the constriction of MAs induced by U 46619 in a manner of concentration dependency, and the dilatation capability was reversed by L-NAME. This effect was significantly dependent on the intactness of MA endothelium, accompanying an increment of NO production in mesenteric arterial endothelium cells. The increment of NO production was reversed by inhibiting the PKA. Also, the expression of p-eNOS was activated by HSYA shown in Western Blot assays. The cells imaging revealed a significant increase and drop of the influx of Ca These findings suggest that HSYA exerts vessel dilation effect on MAs via a TRPV4-dependent influx of Ca
Identifiants
pubmed: 32234595
pii: S0378-8741(20)30179-3
doi: 10.1016/j.jep.2020.112790
pii:
doi:
Substances chimiques
Quinones
0
TRPV Cation Channels
0
Trpv4 protein, rat
0
Vasodilator Agents
0
hydroxysafflor yellow A
146087-19-6
Nitric Oxide
31C4KY9ESH
Chalcone
5S5A2Q39HX
Calcium
SY7Q814VUP
NG-Nitroarginine Methyl Ester
V55S2QJN2X
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
112790Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.