Sadraei Hassan, Asghari Gholamreza, Alinejad Mahla
Department of Pharmacology and Toxicology, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, I.R. Iran.
Department of Pharmacognosy and Isfahan Pharmaceutical Sciences Research Center, Isfahan University of Medical Sciences, Isfahan, I.R. Iran.
Res Pharm Sci. 2016 Jul;11(4):284-92. doi: 10.4103/1735-5362.189295.
Dracocephalum kotschyi Boiss. is a traditional medicine with antispasmodic activities. The objective of this research was to study antispasmodic activities of hydroalcoholic extract of D. kotschyi on rat isolated uterus contractions for comparison with isolated ileum. Hydroalcoholic extract was obtained from aerial part of D. kotschyi using percolation method. A portion of rat ileum or uterus was suspended in Tyrode's solution at 37°C and gassed with O2. Effect of D. kotschyi extract was assessed on ileum or uterus contractions induced by KCl (80 mM), acetylcholine (ACh, 500 nM), electrical field stimulation (EFS) or oxytocin (0.0005 IU/mL). The extract of D. kotschyi concentration-dependently inhibited ileum responses to KCl (IC50 = 65 ± 18 μg/mL), ACh (IC50 = 102 ± 18 μg/mL) and EFS (IC50 = 117 ± 29 μg/mL). The extract of D. kotschyi also concentration-dependently inhibited uterus responses to KCl (IC50 = 453 ± 64μg/mL), ACh (IC50 = 58 ± 9 μg/mL), EFS (IC50 = 22 ± 3 μg/mL) as well as oxytocin (IC50 = 70 ± 11 μg/mL). From this experiment it was concluded that D. kotschyi extract possesses antispasmodic activities on both smooth muscle of ileum and uterus. In comparison, the extract was more effective inhibitor of ACh and EFS responses in rat uterus than on the ileum. On the other hand, the extract was a more potent inhibitor of KCl response on rat ileum. However, the extract was found to be a potent inhibitor of oxytocin-induced contraction of rat uterus. These results indicate that D. kotschyi extract may contain components that might be useful lead compounds for prevention of uterus spasm.
科氏青兰是一种具有解痉活性的传统药物。本研究的目的是研究科氏青兰水醇提取物对大鼠离体子宫收缩的解痉活性,并与离体回肠进行比较。采用渗漉法从科氏青兰地上部分获得水醇提取物。将一部分大鼠回肠或子宫悬浮于37℃的台氏液中,并用O₂通气。评估科氏青兰提取物对由氯化钾(80 mM)、乙酰胆碱(ACh,500 nM)、电场刺激(EFS)或催产素(0.0005 IU/mL)诱导的回肠或子宫收缩的影响。科氏青兰提取物浓度依赖性地抑制回肠对氯化钾(IC50 = 65 ± 18 μg/mL)、乙酰胆碱(IC50 = 102 ± 18 μg/mL)和电场刺激(IC50 = 117 ± 29 μg/mL)的反应。科氏青兰提取物还浓度依赖性地抑制子宫对氯化钾(IC50 = 453 ± 64μg/mL)、乙酰胆碱(IC50 = 58 ± 9 μg/mL)、电场刺激(IC50 = 22 ± 3 μg/mL)以及催产素(IC50 = 70 ± 11 μg/mL)的反应。从该实验得出结论,科氏青兰提取物对回肠和子宫的平滑肌均具有解痉活性。相比之下,该提取物对大鼠子宫中乙酰胆碱和电场刺激反应的抑制作用比对回肠更有效。另一方面,该提取物对大鼠回肠中氯化钾反应的抑制作用更强。然而,发现该提取物是催产素诱导的大鼠子宫收缩的有效抑制剂。这些结果表明,科氏青兰提取物可能含有可作为预防子宫痉挛的有用先导化合物的成分。