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首页> 外文期刊>International Journal of Basic & Clinical Pharmacology >Preliminary pharmacological investigation of the ischuretic property and safety of a hydro-ethanolic extract of Amaranthus spinosis (Fam: Amaranthaceae)
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Preliminary pharmacological investigation of the ischuretic property and safety of a hydro-ethanolic extract of Amaranthus spinosis (Fam: Amaranthaceae)

机译:mar菜的水-乙醇提取物的缺血性和安全性的初步药理研究(家族:A菜科)

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Background: Ischuria is a health and social problem, having a negative impact on sufferers. This study therefore was a preliminary investigation of the ischuretic property and safety for use of a hydro-ethanolic extract of Amaranthus spinosus used traditionally in managing ischuria. Methods: Phytochemical screening, thin layer chromatography and high performance liquid chromatography were performed on the extract to establish fingerprints for identification. Acetylcholine, Nicotine, and the extract were applied to an isolated rat urinary bladder to ascertain contractile response. The possible receptor site(s) of action was also investigated using isolated rabbit jejunum, and guinea-pig ileum preparations. In-house observation, hematological analysis, and liver and kidney function tests were performed on Sprague-Dawley rats, in acute and sub-acute toxicity studies. Results: The extract had contractile effects on the rat urinary bladder (similar to acetylcholine and nicotine) and rabbit jejunum. Its contractile effect of the guinea-pig ileum was significantly inhibited by hexamethonium (77.50 ± 8.50 %; P ≤ 0.001) and to a lesser extent by mepyramine (49.2 ± 6.80 %; P ≤ 0.001) and Atropine (22.45 ± 5.22 %; P ≤ 0.01). The extract (80-800 mg kg-1) was not lethal and a 160 and 240 mg kg-1 dose had no adverse effect on blood, liver, kidney metabolic function. Conclusions: The hydro-ethanolic extract of Amaranthus spinosus has ischuretic activity possibly mediated via nicotinic, histaminic and muscarinic receptor stimulation and is safety to use in ischuria.
机译:背景:缺血是一个健康和社会问题,对患者造成负面影响。因此,本研究是对传统上用于处理坐骨神经的A菜的氢乙醇提取物的镇静特性和安全性的初步研究。方法:对提取物进行植物化学筛选,薄层色谱和高效液相色谱法建立指纹图谱进行鉴定。将乙酰胆碱,尼古丁和提取物应用于分离的大鼠膀胱,以确定收缩反应。还使用分离的兔空肠和豚鼠回肠制剂研究了可能的受体作用位点。在急性和亚急性毒性研究中,对Sprague-Dawley大鼠进行了内部观察,血液学分析以及肝肾功能测试。结果:提取物对大鼠膀胱(类似于乙酰胆碱和尼古丁)和家兔空肠均有收缩作用。六甲铵(77.50±8.50%; P≤0.001)显着抑制其对豚鼠回肠的收缩作用,甲美拉明(49.2±6.80%; P≤0.001)和阿托品(22.45±5.22%; P ≤0.01)。提取物(80-800 mg kg-1)没有致死性,160和240 mg kg-1剂量对血液,肝脏,肾脏的代谢功能无不利影响。结论:A菜的水乙醇提取物具有可能通过烟碱,组织蛋白和毒蕈碱受体刺激介导的局部缺血活性,并且在坐骨结节中使用安全。

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