FOLLOWUS
1. Experiment and Research Center, Xiyuan Hospital, China Academy of Chinese Medical Sciences,Beijing,China
2. Department of Pharmacology, College of Medicine, Xi’an Jiaotong University,Xi’an,China
纸质出版日期:2013,
网络出版日期:2013-7-2,
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Zhang, Jy., Cao, Yx., Weng, Wl. et al. Paeonol induces vasodilatation in rat mesenteric artery via inhibiting extracellular Ca2+ influx and intracellular Ca2+ release., Chin. J. Integr. Med. 19, 510–516 (2013). https://doi.org/10.1007/s11655-013-1505-8
Jin-yan Zhang, Yong-xiao Cao, Wei-liang Weng, et al. Paeonol induces vasodilatation in rat mesenteric artery via inhibiting extracellular Ca2+ influx and intracellular Ca2+ release[J]. Chinese Journal of Integrative Medicine, 2013,19(7):510-516.
Zhang, Jy., Cao, Yx., Weng, Wl. et al. Paeonol induces vasodilatation in rat mesenteric artery via inhibiting extracellular Ca2+ influx and intracellular Ca2+ release., Chin. J. Integr. Med. 19, 510–516 (2013). https://doi.org/10.1007/s11655-013-1505-8 DOI:
Jin-yan Zhang, Yong-xiao Cao, Wei-liang Weng, et al. Paeonol induces vasodilatation in rat mesenteric artery via inhibiting extracellular Ca2+ influx and intracellular Ca2+ release[J]. Chinese Journal of Integrative Medicine, 2013,19(7):510-516. DOI: 10.1007/s11655-013-1505-8.
To investigate the vasodilative effect of paeonol in rat mesenteric artery and the mechanisms responsible for it. Rats were anaesthetized and sacrificed. The superior mesenteric artery was removed
dissected free of adherent tissue and cut into 2.0 mm long cylindrical segments. Isometric tension of artery rings was recorded by a myograph system in vitro. Concentration-relaxation curves of paeonol (17.8 μ mol/L to 3.16 mmol/L) were recorded on artery rings precontracted by potassium chloride (KCl) and concentration-contraction curves of KCl
5-hydroxytryptamine (5-HT)
noradrenaline (NA) or calcium chloride (CaCl2) were recorded in the presence of paeonol (10−4.5
10−3.8
10−3.5 mol/L) respectively. And also
concentrationrelaxation curves of paeonol were recorded in the presence of different potassium channel inhibitors and propranolol on rings precontracted with KCl respectively. To investigate the role of intracellular Ca2+ release from Ca2+ store
the contraction induced by NA (100 μ mol/L) and CaCl2 (2 mmol/L) in Ca2+ free medium was observed in the presence of paeonol respectively. Paeonol relaxed artery rings precontracted by KCl in a concentration-dependent manner and the vasodilatation effect was not affected by endothelium denudation. Paeonol significant decreased the maximum contractions (Emax) induced by KCl
CaCl2
NA and 5-HT
as well as Emax induced by NA and CaCl2 in Ca2+ -free medium
suggesting that paeonol dilated the artery via inhibiting the extracellular Ca2+ influx mediated by voltage-dependent calcium channel
and receptor-mediated Ca2+-influx and release. Moreover
none of glibenclamide
tetraethylammonium
barium chlorded and propranolol affected the paeonol-induced vasodilatation
indicating that the vasodilatation was not contributed to ATP sensitive potassium channel
calcium-activated potassium channel
inwardly rectifying potassium channel
and β-adrenoceptor. Paeonol induces non-endothelium dependent-vasodilatation in rat mesenteric artery via inhibiting voltage-dependent calcium channel-mediated extracellular Ca2+ influx and receptor-mediated Ca2+ influx and release.
To investigate the vasodilative effect of paeonol in rat mesenteric artery and the mechanisms responsible for it. Rats were anaesthetized and sacrificed. The superior mesenteric artery was removed
dissected free of adherent tissue and cut into 2.0 mm long cylindrical segments. Isometric tension of artery rings was recorded by a myograph system in vitro. Concentration-relaxation curves of paeonol (17.8 μ mol/L to 3.16 mmol/L) were recorded on artery rings precontracted by potassium chloride (KCl) and concentration-contraction curves of KCl
5-hydroxytryptamine (5-HT)
noradrenaline (NA) or calcium chloride (CaCl2) were recorded in the presence of paeonol (10−4.5
10−3.8
10−3.5 mol/L) respectively. And also
concentrationrelaxation curves of paeonol were recorded in the presence of different potassium channel inhibitors and propranolol on rings precontracted with KCl respectively. To investigate the role of intracellular Ca2+ release from Ca2+ store
the contraction induced by NA (100 μ mol/L) and CaCl2 (2 mmol/L) in Ca2+ free medium was observed in the presence of paeonol respectively. Paeonol relaxed artery rings precontracted by KCl in a concentration-dependent manner and the vasodilatation effect was not affected by endothelium denudation. Paeonol significant decreased the maximum contractions (Emax) induced by KCl
CaCl2
NA and 5-HT
as well as Emax induced by NA and CaCl2 in Ca2+ -free medium
suggesting that paeonol dilated the artery via inhibiting the extracellular Ca2+ influx mediated by voltage-dependent calcium channel
and receptor-mediated Ca2+-influx and release. Moreover
none of glibenclamide
tetraethylammonium
barium chlorded and propranolol affected the paeonol-induced vasodilatation
indicating that the vasodilatation was not contributed to ATP sensitive potassium channel
calcium-activated potassium channel
inwardly rectifying potassium channel
and β-adrenoceptor. Paeonol induces non-endothelium dependent-vasodilatation in rat mesenteric artery via inhibiting voltage-dependent calcium channel-mediated extracellular Ca2+ influx and receptor-mediated Ca2+ influx and release.
paeonolvasodilatationcontractionrat mesenteric arterycalcium
paeonolvasodilatationcontractionrat mesenteric arterycalcium
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