Sadraei H, Shokoohinia Y, Sajjadi S E, Mozafari M
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. 2013 Apr;8(2):137-44.
Prangos ferulacea is a plant found in the Mediterranean and Middle-east regions used as carminative, anti-flatulent, emollient and antibacterial herb. It is believed that the coumarins are responsible for some of known effects of Prangos. In this research the relaxant effects of P. ferulacea coumrin rich extract as well as osthole as its main prenylated coumarins were investigated on rat ileum contraction in vitro. Relaxant effect of osthole and P. ferulacea extract were examined on contraction induced by KCl, acetylcholine (ACh) and electrical field stimulation (EFS) and compared with propantheline and nifedipine. The acetone extract of P. ferulacea concentration-dependently relaxed ileum contraction induced by KCl (IC50=1.3 ± 0.25 μg/ml), ACh (IC50=7.7 ± 1.1 μg/ml) and EFS (IC50=8.8 ± 1.4 μg/ml), while, the extract at lower concentration (4 μg/ml) potentiated the ACh and EFS responses. Unlike the extract, osthole did not potentiate the ileum contraction but concentration-dependently inhibited ileum contractile responses to KCl (IC50=2.2 ± 0.7 μg/ml), ACh (IC50=2.5 ± 0.7 μg/ml) and EFS (IC50=2.8 ± 0.24 μg/ml). Propantheline concentration dependently inhibited the ileum response to ACh, with IC50 value of 0.61 ± 0.09nM without affecting the KCl response. As expected, the EFS response was only partially reduced. Nifedipine (0.2-50 nM) inhibited tonic contraction induced by KCl with IC50 value of 2.5 ± 0.8 nM but only partially inhibited the response to ACh. However, the response to EFS was reduced only by 33%. These results confirmed both potentiatory and inhibitory action of P. ferulacea extract on rat ileum contractile activity. Osthole is responsible for the inhibitory effect but potentiating components are not yet known.
阿魏芹是一种生长在地中海和中东地区的植物,用作驱风、防肠胃胀气、润肤和抗菌草药。据信,香豆素是阿魏芹某些已知功效的原因。在本研究中,研究了富含阿魏芹香豆素的提取物以及作为其主要异戊烯基化香豆素的蛇床子素对大鼠离体回肠收缩的松弛作用。检测了蛇床子素和阿魏芹提取物对氯化钾、乙酰胆碱(ACh)和电场刺激(EFS)诱导的收缩的松弛作用,并与丙胺太林和硝苯地平进行比较。阿魏芹的丙酮提取物浓度依赖性地松弛了由氯化钾(IC50=1.3±0.25μg/ml)、乙酰胆碱(IC50=7.7±1.1μg/ml)和电场刺激(IC50=8.8±1.4μg/ml)诱导的回肠收缩,而较低浓度(4μg/ml)的提取物增强了乙酰胆碱和电场刺激的反应。与提取物不同,蛇床子素没有增强回肠收缩,但浓度依赖性地抑制了回肠对氯化钾(IC50=2.2±0.7μg/ml)、乙酰胆碱(IC50=2.5±0.7μg/ml)和电场刺激(IC50=2.8±0.24μg/ml)的收缩反应。丙胺太林浓度依赖性地抑制回肠对乙酰胆碱的反应,IC50值为0.61±0.09nM,而不影响氯化钾反应。正如预期的那样,电场刺激反应仅部分降低。硝苯地平(0.2-50nM)抑制由氯化钾诱导的强直性收缩,IC50值为2.5±0.8nM,但仅部分抑制对乙酰胆碱的反应。然而,对电场刺激的反应仅降低了33%。这些结果证实了阿魏芹提取物对大鼠回肠收缩活性的增强和抑制作用。蛇床子素是产生抑制作用的原因,但增强作用的成分尚不清楚。