School of Pharmaceutical Sciences, Discipline of Pharmaceutical Chemistry, Universiti Sains Malaysia, Penang, Malaysia.
School of Pharmaceutical Sciences, Discipline of Pharmacology, Universiti Sains Malaysia, Penang, Malaysia.
Phytother Res. 2019 Mar;33(3):660-675. doi: 10.1002/ptr.6255. Epub 2019 Jan 17.
The Dillenia suffruticosa leaves (Dilleniaceae), a folk medicine recommended in Southeast Asia for treating inflammation, were phytochemically studied for the first time and assessed for suppression of λ-carrageenan-induced paw oedema in rats. The crude methanolic extract orally administered at 5,000 mg/kg, displayed no toxicity and at 250 to 1,000 mg/kg significantly suppressed the paw oedema. Two-isolated triterpenoids, betulinic acid (1) and koetjapic acid (2) orally administered at 50 mg/kg, significantly reduced the paw oedema, (p < 0.001) and (p < 0.005) at the fourth h onwards to 47.36% ± 2.23 and 53.43% ± 7.09, respectively, from 95.90% ± 6.88 oedema induced by λ-carrageenan alone. 1 and the isolated flavonoids of vitexin (3), tiliroside (4), and kaempferol (5), displayed moderately more of cyclooxygenase (COX)-2 than COX-1 enzyme inhibition, whereas 2 was slightly more inhibition of COX-1. The in silico molecular docking studies provided support to the in vitro COX studies that the isolated compounds formed H-bonding with the amino acid residues at the COX-2 catalytic sites. The triterpenoids were bound to the peroxidase, possibly inhibiting the peroxidase reaction, whereas the flavonoids interacted more at the cyclooxygenase, resembling celecoxib, therefore providing evidences that these compounds were responsible for the anti-inflammatory properties of D. suffruticosa.
杜茎山的叶子(山榄科),在东南亚作为治疗炎症的民间药物而被推荐,首次进行了植物化学研究,并评估了其对大鼠角叉菜胶诱导的足肿胀的抑制作用。口服给予 5000mg/kg 的粗甲醇提取物没有显示出毒性,并且在 250 至 1000mg/kg 时显著抑制了足肿胀。两种分离的三萜酸,白桦脂酸(1)和柯桠酸(2),口服给予 50mg/kg,显著减少了足肿胀,(p<0.001)和(p<0.005),从单独的角叉菜胶诱导的 95.90%±6.88%到 47.36%±2.23%和 53.43%±7.09%,分别从 95.90%±6.88%到 47.36%±2.23%和 53.43%±7.09%。1 和分离的黄酮类化合物牡荆素(3)、荭草苷(4)和山柰酚(5),对环氧化酶(COX)-2的抑制作用比 COX-1 酶更显著,而 2 对 COX-1 的抑制作用略强。计算机分子对接研究为体外 COX 研究提供了支持,即分离的化合物与 COX-2 催化部位的氨基酸残基形成氢键。三萜类化合物与过氧化物酶结合,可能抑制过氧化物酶反应,而黄酮类化合物在环氧化酶处相互作用更多,类似于塞来昔布,因此提供了这些化合物负责杜茎山抗炎特性的证据。