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Extraction and phytochemical investigation of Calotropis procera : Effect of plant extracts on the activity of diverse muscles

机译:Calotropis procera的提取和植物化学研究:植物提取物对不同肌肉活性的影响。

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Context : Calotropis procera (Ait.) R.Br. (Asclepiadaceae) is a shrub or small tree that grows wild in Egypt. Calotropis acts as a purgative, anthelmintic, anticoagulant, palliative (in problems with respiration, blood pressure), antipyretic, and analgesic, and induces neuromuscular blocking activity. Little research has been done to study the electrophysiological effects of this plant’s extracts on cardiac, smooth, and skeletal muscle activities. Objective : The present study was conducted to determine the phytochemical composition and the effect of the total alcohol extract of the shoot of the plant, which contains almost all of C. procera ’s cardiac glycosides, flavonoids, and saponins. Also, this study attempted to throw more light on the electrophysiological effects of the plant extracts on cardiac, smooth, and skeletal muscle activities and to clarify the mechanism(s) of their observed action(s). Materials and methods : The aerial parts of the plant were air dried and their ethanol extracts partitioned with successive solvents. Cardiac, smooth, and skeletal muscles were used in this study to investigate the physiological and pharmacological effects of the plant extracts from different solvents. The data were analyzed by paired t -test. Results : The phytochemical investigation of Calotropis procera revealed the presence of cardenolides, flavonoids, and saponins. The effects of ethanol, n -butanol, and ethyl acetate (EtOAc) extracts were each evaluated on isolated toad heart and their mechanisms of action determined. Perfusion with 2 μg/mL ethanol, 0.2 μg/mL butanol, and 0.2 μg/mL EtOAc extracts caused a significant decrease in heart rate (bradycardia), significant increase in the force of ventricular contraction, and increase in T-wave amplitude. In addition, the effects of different extracts of the studied plant on smooth muscle and skeletal muscle were investigated in this study. The different extracts and latex of C. procera induced a negative chronotropic effect and decreased the heart rate (HR) of isolated toad heart. The different extracts increased the power of contraction of the duodenum (trace a). Pretreatment with atropine sulfate as a muscarinic receptor blocker abolished the stimulatory effect of the different plant extracts and latex of C. procera (trace b). Discussion : The present data suggest that ethanol, butanol, and EtOAc extracts of Calotropis procera have negative chronotropism and positive inotropism. Verapamil could abolish the inotropic effect of ethanol as well as that of butanol and EtOAc extracts. Meanwhile, atropine did not abolish the observed negative chronotropic effect. The ethanol extract increased the power of contraction of rabbit duodenum, but atropine abolished this effect. It also decreased the skeletal muscle contraction; this effect could be through blocking of the nicotinic receptors. Butanol and EtOAc extract data for smooth and skeletal muscles are very close to those for the corresponding ethanol extract of the studied plant. The present data for C . procera indicate its direct action on the myocardium, its increase of smooth muscle motility, and its relaxation of skeletal muscle contraction. The chemical constituents could directly affect the cell membrane probably through receptors coupling to G proteins. They regulate the ion channel physiology as in the myocardium. Conclusion : The present data on the extracts of C . procera indicate a direct action on the myocardium, stimulatory effect on smooth muscle motility, and relaxant action on skeletal muscle contraction. Chemical constituents could directly affect the cell membrane probably through receptors coupling to G proteins. They regulate the ion channel physiology as in the myocardium.
机译:背景:Calotropis procera(Ait。)R.Br. (Asclepiadaceae)是在埃及野生的灌木或小树。 Calotropis用作泻药,驱虫药,抗凝药,姑息药(在呼吸,血压问题上),退热药和镇痛药,并诱导神经肌肉阻滞活性。研究这种植物提取物对心脏,平滑肌和骨骼肌活动的电生理影响的研究很少。目的:进行本研究以确定植物芽的植物化学组成和总酒精提取物的作用,其中几乎包含proc procera的强心苷,类黄酮和皂苷。另外,该研究试图进一步阐明植物提取物对心肌,平滑肌和骨骼肌活动的电生理作用,并阐明其观察到的作用机理。材料和方法:将植物的地上部分风干,并用连续的溶剂分配乙醇提取液。在这项研究中,使用了心肌,平滑肌和骨骼肌来研究不同溶剂中植物提取物的生理和药理作用。通过配对t检验分析数据。结果:Calotropis procera的植物化学研究显示存在心得安,类黄酮和皂苷。分别在分离的蟾蜍心脏上评估了乙醇,正丁醇和乙酸乙酯(EtOAc)提取物的作用,并确定了其作用机理。用2μg/ mL乙醇,0.2μg/ mL丁醇和0.2μg/ mL EtOAc提取物灌注会导致心率(心动过缓)显着降低,心室收缩力显着增加以及T波振幅增加。此外,本研究还研究了不同植物提取物对平滑肌和骨骼肌的影响。 C. procera的不同提取物和胶乳会引起负变时作用,并降低离体蟾蜍心的心率(HR)。不同的提取物增加了十二指肠的收缩能力(迹线a)。用硫酸阿托品作为毒蕈碱受体阻滞剂进行的预处理消除了不同植物提取物和proc procera乳胶的刺激作用(迹线b)。讨论:目前的数据表明,Calotropis procera的乙醇,丁醇和EtOAc提取物具有负变时性和正变力性。维拉帕米可以消除乙醇以及丁醇和EtOAc提取物的正性肌力作用。同时,阿托品没有消除观察到的负面变时效应。乙醇提取物增加了兔十二指肠的收缩能力,但阿托品取消了该作用。它还减少了骨骼肌的收缩。这种作用可能是通过阻断烟碱样受体。平滑肌和骨骼肌的丁醇和EtOAc提取物数据与研究植物的相应乙醇提取物的数据非常接近。 C的当前数据。 procera表示其对心肌的直接作用,平滑肌运动的增强以及骨骼肌收缩的松弛。化学成分可能直接通过与G蛋白偶联的受体直接影响细胞膜。它们调节心肌中的离子通道生理。结论:有关C的提取物的现有数据。 procera表示对心肌有直接作用,对平滑肌运动有刺激作用,对骨骼肌收缩有松弛作用。化学成分可能通过与G蛋白偶联的受体直接影响细胞膜。它们调节心肌中的离子通道生理。

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    《Pharmaceutical Biology》 |2010年第10期|共111页
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