The Relaxant Activity of Safranal in Isolated Rat Aortas is Mediated Predominantly via an Endothelium-Independent Mechanism -Vasodilatory mechanism of safranal-

Objectives: Safranal is a pharmacologically active component of saffron and is responsible for the unique aroma of saffron. The hypotensive effect of safranal has been shown in previous studies. This study evaluates the mechanism for the vasodilatory effects induced by safranal on isolated rat aorta...

Full description

Saved in:
Bibliographic Details
Main Authors: Bibi Marjan Razavi (Author), Mojtaba Alipoor Amanloo (Author), Mohsen Imenshahidi (Author), Hossein Hosseinzadeh (Author)
Format: Book
Published: Korean Pharmacopuncture Institute, 2016-12-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_ba8755591a964a0aa2ee812e11f64ca8
042 |a dc 
100 1 0 |a Bibi Marjan Razavi  |e author 
700 1 0 |a Mojtaba Alipoor Amanloo  |e author 
700 1 0 |a Mohsen Imenshahidi  |e author 
700 1 0 |a Hossein Hosseinzadeh  |e author 
245 0 0 |a The Relaxant Activity of Safranal in Isolated Rat Aortas is Mediated Predominantly via an Endothelium-Independent Mechanism -Vasodilatory mechanism of safranal- 
260 |b Korean Pharmacopuncture Institute,   |c 2016-12-01T00:00:00Z. 
500 |a 2093-6966 
500 |a 2234-6856 
500 |a 10.3831/KPI.2016.19.034 
520 |a Objectives: Safranal is a pharmacologically active component of saffron and is responsible for the unique aroma of saffron. The hypotensive effect of safranal has been shown in previous studies. This study evaluates the mechanism for the vasodilatory effects induced by safranal on isolated rat aortas. Methods: To study the vasodilatory effects of safranal (0.2, 0.4 and 0.8 mM), we contracted isolated rat thoracic aorta rings by using 10-6-M phenylephrine (PE) or 80-mM KCl. Dimethyl sulfoxide (DMSO) was used as a control. The vasodilatory effect of safranal was also evaluated both on intact and denuded endothelium aortic rings. Furthermore, to study the role of nitric oxide and prostacyclin in the relaxation induced by safranal, we incubated the aortic rings by using L-NAME (10-6 M) or indomethacin (10-5 M), each for 20 minutes. Results: Safranal induced relaxation in endothelium-intact aortic rings precontracted by using PE or KCl in a concentration-dependent manner, with a maximum relaxation of more than 100%. The relaxant activity of safranal was not eliminated by incubating the aortic rings with L-NAME (EC50 = 0.29 vs. EC50 = 0.43) or with indomethacin (EC50 = 0.29 vs. EC50 = 0.35), where EC50 is the half maximal effective concentration. Also, the vasodilatory activity of safranal was not modified by endothelial removal. Conclusion: This study indicated that relaxant activity of safranal is mediated predominantly through an endothelium- independent mechanism. 
546 |a EN 
546 |a KO 
690 |a aorta ring 
690 |a indomethacin 
690 |a L-NAME 
690 |a saffron 
690 |a vasodilatory effect 
690 |a Medicine 
690 |a R 
690 |a Miscellaneous systems and treatments 
690 |a RZ409.7-999 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Journal of Pharmacopuncture, Vol 19, Iss 4, Pp 329-335 (2016) 
787 0 |n http://dx.doi.org/10.3831/KPI.2016.19.034 
787 0 |n https://doaj.org/toc/2093-6966 
787 0 |n https://doaj.org/toc/2234-6856 
856 4 1 |u https://doaj.org/article/ba8755591a964a0aa2ee812e11f64ca8  |z Connect to this object online.