In vitro and In vivo Investigations Provide New Insights into Bioactivities of Blumea clarkei Hook.f. Leaves

Farzana Kabir, Asif Uj Jaman, Rizia Azad Rumpa, Tabassum Jannat, Safaet Alam, Tanoy Saha, Ashraful Islam, Mahfuza Afroz Soma
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引用次数: 5

Abstract

As there is a resurgence of interest in plants as promising sources of new active pharmaceutical constituents, the present study has been designed to establish the preliminary biological activities of Blumea clarkei Hook.f. leaves. Here, the crude methanol extract of the leaves along with its organic and aqueous soluble fractions were subjected to different in vitro and in vivo assays. The ethyl acetate soluble fraction exhibited the highest total phenolic content (71.59 mg of GAE/gm of extract) and DPPH free radical scavenging (IC50 value 19.25 μg/ml) whereas another polar fraction; the aqueous soluble extractive showed the maximum cytotoxicity (LC50 value of 18.60 μg/ml) in the brine shrimp lethality assay. In membrane stabilizing activity evaluation, the inhibition of hypotonic solution and heat induced hemolysis were revealed maximum by the DCM (30.64%) and aqueous soluble fraction (39.15%), respectively while the crude methanol extract exhibited the highest thrombolytic potential (30.47% clot lysis). The central analgesic activity of the crude extract significantly increased the latent response time in tail-immersion method (p<0.001) at doses 200 and 400 mg/kg of body weight after 90 minutes of administration when compared to the control group. In acetic acid-induced writhing method, the plant extract showed prominent peripheral analgesia (p<0.001) with 47.54% and 65.57% inhibition at 200- and 400-mg/kg of body weight, respectively. In addition, a dose dependent hypoglycemic and antidiarrheal activities were also observed by the crude extract. Bangladesh Pharmaceutical Journal 24(2): 149-158, 2021
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体外和体内研究为蓝麦的生物活性提供了新的见解。叶子
随着对植物作为新的活性药物成分的有希望的来源的兴趣的复苏,本研究的目的是建立Blumea clarkei Hook.f的初步生物活性。叶子。在这里,粗甲醇提取物的叶片及其有机和水溶性部分进行了不同的体外和体内的测定。乙酸乙酯可溶性部位总酚含量最高(71.59 mg GAE/gm),清除DPPH自由基的IC50值最高(19.25 μg/ml);在盐水对虾致死实验中,水溶性提取物的细胞毒性最大,LC50值为18.60 μg/ml。在膜稳定活性评价中,DCM和水溶性部分对低渗溶液和热溶血的抑制作用最大(分别为30.64%和39.15%),而粗甲醇提取物具有最高的溶栓潜力(30.47%)。与对照组相比,在给药90分钟后,200和400 mg/kg体重的粗提物的中枢镇痛活性显著增加了尾浸法的潜伏反应时间(p<0.001)。在醋酸扭体法中,200 mg/kg和400 mg/kg时,植物提取物的外周镇痛作用显著(p<0.001),抑制率分别为47.54%和65.57%。此外,还观察到粗提物具有剂量依赖性的降糖和止泻活性。孟加拉国药学杂志24(2):149-158,2021
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