Title of article
Antispasmodic effect of osthole and Prangos ferulacea extract on rat uterus smooth muscle motility
Author/Authors
Sadraei، H. نويسنده , , Shokoohinia، Y. نويسنده Department of Pharmacognosy and Biotechnology, School of Pharmacy, Kermanshah University of Medical Sciences, I.R. Iran. , , Sajjadi، SE نويسنده 2- Department of Pharmacognosy, School of Pharmacy and Pharmaceutical Science, Isfahan, Iran Sajjadi, SE , Ghadirian، B. نويسنده Department of Pharmacology and Isfahan Pharmaceutical Sciences Research Center, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, I.R. Iran. ,
Issue Information
دوماهنامه با شماره پیاپی 0 سال 2012
Pages
9
From page
141
To page
149
Abstract
Several species of Prangos are traditionally used as emollient, carminative, tonic, anti-flatulent, anthelmintic and anti-thrombotic agents. Osthole, a coumarin isolated from Prangos, are believed to be responsible for some of its effects. In this research, relaxant effects of Prangos ferulacea extract and osthole on rat uterus contraction induced by KCl, acetylcholine (ACh), oxytocin and electrical field stimulation (EFS) was investigated and compared with atropine and salbutamol. P. ferulacea acetonic extract concentration-dependently relaxed uterine contraction induced by KCl (IC50=13 ± 0.81 ?g/ml), ACh (IC50=12 ± 1.38 ?g/ml), oxytocin (IC50=16 ± 3.14 ?g/ml) and EFS (IC50=11 ± 1.5 ?g/ml). However, the extract at lower concentration (2.5 µg/ml) potentiated the EFS response. Osthole only had inhibitory effect on rat uterus and its relaxant effect was observed at lower concentration in comparison with P. ferulacea extract. Osthole in a similar way inhibited the response to KCl (IC50=4 ± 0.13 ?g/ml), ACh (IC50=4 ± 0.8 ?g/ml), oxytocin (IC50=4 ± 0.8 ?g/ml) and EFS (IC50=1.5 ± 0.5 ?g/ml). Our results demonstrated that osthole acted directly on uterus smooth muscle to induce relaxation, whereas P. ferulacea caused both contraction and relaxation of rat uterine smooth muscle. The relaxation of osthole might be mediated through Ca2+ channel blocking activity as it inhibited the response to KCl. Mechanisms other than Ca2+ channel blocking appeared to be responsible for ACh relaxation effect of osthole.
Journal title
Research in Pharmaceutical Sciences
Serial Year
2012
Journal title
Research in Pharmaceutical Sciences
Record number
1216339
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