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Dichrostachys cinerea (L.) Wight et Arn (Mimosaceae) hydro-alcoholic extract action on the contractility of tracheal smooth muscle isolated from guinea-pig

机译:灰(L.)Wight et Arn(含羞草科)的水-醇提取物对豚鼠气管平滑肌收缩力的作用

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Background Dichrostachys cinerea (L.) Wight et Arn. (Mimosaceae) is largely used in ethno-medically across Africa, and mainly employed for the treatment of asthma in Ivory Coast and Gabon. The paper analyses the relaxation induced by the methanolic extract of D. cinerea (Edici) in the guinea-pig trachea preparations (GPTPs). Purpose: This study aimed to bring out the scientific basis to the use of this plant leading to the validation of this phytomedicine. Method The aorta obtained from guinea-pigs was immediately placed in a Mac Ewen solution. Experiments were performed in preparations suspended between two L-shaped stainless steel hooks in a 10 ml organ bath containing Mac Ewen solution. The isometric contractile force of the aorta strips of guinea-pig were recorded by using a strain gauge. The different drugs were directly administered into the organ bath and the magnitude of GPTPs was evaluated. Results Phytochemical analysis of the methanolic extract of Dichrostachys cinerea (Edici) using chemical methods revealed the presence of flavenoids, tannins, sterols, triterpenes and polyphenols. Pharmacological studies performed in GPTPs show that of Dichrostachys cinerea (0.1 mg/ml - 2 mg/ml) evoked a broncho-constriction in GPTPs. Whereas, at concentration up to 2 mg/ml, Edici induced a significant dose-dependent relaxation in the GPTPs. KCl-, ACh- or histamine-evoked contractions of isolated trachea was significantly inhibited by increasing concentrations of Edici (3.5-10 mg/ml). Edici (10 mg/ml) as well as promethazine (0.25 mg/ml) significantly inhibited contractions induced by increasing concentrations of histamine (1×10-7-1×10-4mg/ml). In the presence of atropine at a concentration of 10-6mg/ml, contractile response curve (CRC) evoked by ACh (1×10-5-1×10-2 mg/ml) was significantly abolished in concentration-dependent manner. Edici did not significantly reduced ACh evoked contraction (10-5-10-2mg/ml). Conclusion These observations suggest that Edici could act through two mechanisms: firstly by activation of β-adrenergic or histaminergic receptors; and secondly muscarinic receptors may not be greatly involved, that justifying the use of the extract in traditional Medicine in Africa.
机译:背景技术Dichrostachys cinerea(L.)Wight等人。 (Mimosaceae)在非洲的种族医学上广泛使用,主要用于在象牙海岸和加蓬治疗哮喘。本文分析了豚鼠气管制剂(GPTPs)中的D. cinerea(Edici)甲醇提取物引起的松弛。目的:本研究旨在为使用这种植物提供科学依据,从而验证该植物药。方法将豚鼠的主动脉立即置于Mac Ewen溶液中。在悬浮于装有Mac Ewen溶液的10毫升器官浴中的两个L形不锈钢钩之间的制剂中进行实验。通过使用应变仪记录豚鼠主动脉条的等轴测收缩力。将不同的药物直接施用到器官浴中并评估GPTP的强度。结果使用化学方法对Dichrostachys cinerea(Edici)的甲醇提取物进行植物化学分析后,发现存在类黄酮,单宁,固醇,三萜和多酚。在GPTPs中进行的药理研究表明,灰柏(Dichrostachys cinerea)(0.1 mg / ml-2 mg / ml)在GPTPs中引起支气管收缩。而在浓度高达2 mg / ml时,Edici在GPTP中诱导了显着的剂量依赖性弛豫。增加浓度的Edici(3.5-10 mg / ml)可显着抑制KCl,ACh或组胺引起的气管收缩。 Edici(10 mg / ml)和异丙嗪(0.25 mg / ml)显着抑制组胺(1×10 -7 -1×10 -4 mg / ml)。在阿托品浓度为10 -6 mg / ml的情况下,ACh引起的收缩反应曲线(CRC)(1×10 -5 -1×10 < sup> -2 mg / ml)以浓度依赖性方式显着消除。 Edici没有显着降低ACh引起的收缩(10 -5 -10 -2 mg / ml)。结论这些观察结果表明Edici可能通过两种机制起作用:首先是通过激活β-肾上腺素能或组胺能受体;其次是通过激活作用。其次,毒蕈碱受体可能并未参与其中,这证明了该提取物在非洲传统医学中的使用是合理的。

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