In Vivo and in Vitro Anti-Inflammatory Activities of Extracts of Pandiaka angustifolia (Vahl.) Hepper (Amaranthaceae) Used in Traditional Medicine in Burkina Faso

Emmanuel A. M. Thiombiano, M. J. Bangou, Yougbaré-Ziébrou Mouhibatou, M. Kiendrebeogo
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Abstract

Background: Pandiaka angustifolia Valh Hepper (Amaranthaceae) whole plant is used in folk Burkinabe’s medicine to treat ailments with an inflammatory component. Previous studies revealed the antioxidant capacity, xanthine oxidase, and lipoxygenase inhibitory activities of the plant, but to the best of our knowledge, its anti-inflammatory activities were not reported before. Therefore, this study was designed to evaluate the anti-inflammatory and analgesic activity of P. Angustifolia hexane and aqueous extracts using in vitro enzymatic methods and in vivo methods and verify the best anti-inflammatory extract implication in KATP pathways. Experiments: acute toxicity of the plant was conducted under OECD 423 guidelines. Phospholipase and cyclooxygenases were pro-inflammatory enzymes used to evaluate in vitro anti-inflammatory effects of plant extracts while carrageenan induced edema method was used to evaluate the anti-edematous activity and acetic acid inducing writhing method to evaluate the non-morphine analgesic effect of herbal mixture. ATP sensitive K+ channel assay was performed in vivo using the glibenclamide as ATP-sensitive potassium channel (KATP) blocker. Results: enzymatic inhibition assays revealed that both hexane and aqueous extracts of P. angustifolia were good inhibitors against sPLA2 activity with IC50 values of 14.23 ± 0. 72 µg/mL and 11.56 ± 0.11 µg/mL, respectively. Aqueous extract presented the best inhibition for COX-1 (IC50 = 24.76 ±0. 51 µg/mL) while hexane extract concentration that inhibit 50% of COX-2 was lesser than those of aqueous extract. P. angustifolia aqueous extract orally administrated to NMRI mice caused no death at the dose of 3000 mg/kg b.w indicating that the plant toxicity is low. While hexane extract was unable to reduce Carrageenan-induced edema, ethanolic extract were significantly active when extract was orally administrated. Non-morphine analgesic activity evaluation revealed that ethanolic extract was more efficient on writhing reduction than hexane extract. Nociception effect of the plant is linked with its effects on K+ ATP sensitive channels. Conclusion: Results indicate that the anti-inflammatory potential of P. angustifolia may be due to its polar phytoconstituents and observed pharmacological activities provide the scientific basis for the medicinal use of the plant in the treatment of ailment associated with inflammation.
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穿山甲提取物的体内外抗炎活性研究在布基纳法索的传统医学中使用的苋科植物
背景:苋菜科(苋科)全植物在布基纳法索的民间医学中用于治疗具有炎症成分的疾病。以往的研究揭示了该植物的抗氧化能力、黄嘌呤氧化酶和脂氧合酶抑制活性,但据我们所知,其抗炎活性尚未见报道。因此,本研究旨在通过体外酶法和体内法评价红参己烷及其水提物的抗炎和镇痛活性,并验证最佳抗炎提取物在KATP通路中的作用。实验:该植物的急性毒性是根据OECD 423准则进行的。采用磷脂酶和环氧合酶作为促炎酶,评价植物提取物的体外抗炎作用;采用角叉菜胶诱导水肿法评价植物提取物的体外抗炎活性;采用醋酸诱导扭体法评价中药合剂的非吗啡镇痛作用。采用格列本脲作为ATP敏感钾通道(KATP)阻滞剂进行ATP敏感K+通道实验。结果:酶促抑制实验表明,正己烷和水提物均能有效抑制sPLA2活性,IC50值为14.23±0。分别为72µg/mL和11.56±0.11µg/mL。水提液对COX-1的抑制效果最好(IC50 = 24.76±0)。51µg/mL),而正己烷提取物对50% COX-2的抑制作用小于水提物。以3000 mg/kg b.w的剂量口服NMRI小鼠无死亡,表明其植物毒性较低。正己烷提取物不能减轻卡拉胶诱导的水肿,而乙醇提取物在口服时具有显著的活性。非吗啡镇痛活性评价表明,乙醇提取物比己烷提取物更有效地减少扭动。植物的痛觉效应与其对K+ ATP敏感通道的影响有关。结论:研究结果表明,刺叶的抗炎作用可能与其极性植物成分有关,所观察到的药理活性为刺叶治疗炎症相关疾病提供了科学依据。
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