Amin Adnan, Tuenter Emmy, Foubert Kenn, Iqbal Jamhsed, Cos Paul, Maes Louis, Exarchou Vassiliki, Apers Sandra, Pieters Luc
Laboratory of Natural Products and Food Research and Analysis, Department of Pharmaceutical Sciences, University of AntwerpAntwerp, Belgium.
Centre for Advanced Drug Research, COMSATS Institute of Information TechnologyAbbottabad, Pakistan.
Front Pharmacol. 2017 May 1;8:232. doi: 10.3389/fphar.2017.00232. eCollection 2017.
(Wall.) Janch (or (Wall.) Betsche is a well-known medicinal plant in Pakistan that is traditionally used in diabetic and inflammatory conditions. Because little information is available on its phytochemical composition, a range of constituents were isolated and evaluated in assays related to the traditional use. Dried whole plant material was extracted and chromatographically fractionated. Isolated constituents were evaluated and in assays related to the traditional use against diabetes (inhibition of α-glucosidase activity; inhibition of advanced glycation endproducts) and in inflammatory conditions (inhibition of AAPH induced linoleic acid peroxidation, inhibition of 15-LOX, antimicrobial activity). Phytochemical analysis of the extracts and fractions led to isolation of compounds, including the iridoids kickxiasine (being a new compound), mussaenosidic acid, mussaenoside and linarioside; the flavonoids pectolinarigenin and pectolinarin; and 4-hydroxy-benzoic acid methyl ester. The iridoids showed weak antiglycation activity. The flavonoids, however, showed interesting results as pectolinarigenin was highly active compared to pectolinarin. In the α-glucosidase inhibition assay, only weak activity was observed for the iridoids. However, the flavonoid pectolinarigenin showed good activity, followed by pectolinarin. In the 15-LOX experiment, moderate inhibition was recorded for most compounds, the iridoids mussaenosidic acid and mussaenoside being the most active. In the AAPH assay, weak or no inhibition was recorded for all compounds. The assays for the α-glucosidase and 15-LOX assays confirmed the results of respective assays. Pectolinarigenin showed moderate antimicrobial activity against , K1, and , but it was not cytotoxic on a human MRC-5 cell line. Our findings may in part contribute to explain the traditional use of .
(Wall.)Janch(或(Wall.)Betsche)是巴基斯坦一种著名的药用植物,传统上用于治疗糖尿病和炎症。由于关于其植物化学成分的信息很少,因此分离了一系列成分,并在与传统用途相关的试验中进行了评估。将干燥的全株材料进行提取并通过色谱法进行分离。对分离出的成分进行了评估,并在与传统用途相关的试验中检测其对糖尿病的作用(抑制α-葡萄糖苷酶活性;抑制晚期糖基化终产物)以及在炎症条件下的作用(抑制AAPH诱导的亚油酸过氧化、抑制15-脂氧合酶、抗菌活性)。对提取物和分离物进行植物化学分析后,分离出了多种化合物,包括环烯醚萜类化合物kickxiasine(一种新化合物)、马钱子酸、马钱子苷和亚麻苷;黄酮类化合物pectolinarigenin和pectolinarin;以及4-羟基苯甲酸甲酯。环烯醚萜类化合物显示出较弱的抗糖化活性。然而,黄酮类化合物显示出有趣的结果,因为pectolinarigenin比pectolinarin具有更高的活性。在α-葡萄糖苷酶抑制试验中,环烯醚萜类化合物仅表现出较弱的活性。然而,黄酮类化合物pectolinarigenin表现出良好的活性,其次是pectolinarin。在15-脂氧合酶实验中,大多数化合物表现出中等程度的抑制作用,环烯醚萜类化合物马钱子酸和马钱子苷活性最强。在AAPH试验中,所有化合物均表现出较弱或无抑制作用。α-葡萄糖苷酶和15-脂氧合酶试验的结果证实了各自试验的结果。Pectolinarigenin对金黄色葡萄球菌、K1和大肠杆菌表现出中等程度的抗菌活性,但对人MRC-5细胞系无细胞毒性。我们的研究结果可能在一定程度上有助于解释该植物的传统用途。