Sadraei H, Shokoohinia Y, Sajjadi S E, Ghadirian B
Department of Pharmacology and Isfahan Pharmaceutical Sciences Research Center, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, I.R.Iran.
Res Pharm Sci. 2012 Jul;7(3):141-9.
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 (IC(50)=13 ± 0.81 μg/ml), ACh (IC(50)=12 ± 1.38 μg/ml), oxytocin (IC(50)=16 ± 3.14 μg/ml) and EFS (IC(50)=11 ± 1.5 μg/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 (IC(50)=4 ± 0.13 μg/ml), ACh (IC(50)=4 ± 0.8 μg/ml), oxytocin (IC(50)=4 ± 0.8 μg/ml) and EFS (IC(50)=1.5 ± 0.5 μg/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 Ca(2+) channel blocking activity as it inhibited the response to KCl. Mechanisms other than Ca(2+) channel blocking appeared to be responsible for ACh relaxation effect of osthole.
传统上,几种阿魏属植物被用作润肤剂、驱风剂、滋补剂、抗肠胃胀气剂、驱虫剂和抗血栓剂。从阿魏属植物中分离出的香豆素蛇床子素被认为是其某些功效的原因。在本研究中,研究了阿魏提取物和蛇床子素对氯化钾、乙酰胆碱(ACh)、催产素和电场刺激(EFS)诱导的大鼠子宫收缩的松弛作用,并与阿托品和沙丁胺醇进行了比较。阿魏丙酮提取物浓度依赖性地松弛由氯化钾(IC(50)=13±0.81μg/ml)、ACh(IC(50)=12±1.38μg/ml)、催产素(IC(50)=16±3.14μg/ml)和EFS(IC(50)=11±1.5μg/ml)诱导的子宫收缩。然而,较低浓度(2.5μg/ml)的提取物增强了EFS反应。蛇床子素仅对大鼠子宫有抑制作用,与阿魏提取物相比,其在较低浓度下就观察到松弛作用。蛇床子素以类似方式抑制对氯化钾(IC(50)=4±0.13μg/ml)、ACh(IC(50)=4±0.8μg/ml)、催产素(IC(50)=4±0.8μg/ml)和EFS(IC(50)=1.5±0.5μg/ml)的反应。我们的结果表明,蛇床子素直接作用于子宫平滑肌以诱导松弛,而阿魏则引起大鼠子宫平滑肌的收缩和松弛。蛇床子素的松弛作用可能是通过钙(2+)通道阻断活性介导的,因为它抑制了对氯化钾的反应。除钙(2+)通道阻断以外的机制似乎是蛇床子素对ACh松弛作用的原因。