Rauf Abdur, Maione Francesco, Uddin Ghias, Raza Muslim, Siddiqui Bina S, Muhammad Naveed, Shah Syed Uzair Ali, Khan Haroon, De Feo Vincenzo, Mascolo Nicola
Department of Geology, University of Swabi, Khyber Pakhtunkhwa, Anbar 23561, Pakistan.
Department of Pharmacy, University of Naples Federico II, 80131 Naples, Italy.
Evid Based Complement Alternat Med. 2016;2016:4098686. doi: 10.1155/2016/4098686. Epub 2016 Mar 2.
This study deals with the isolation of the active constituent(s) from a methanolic extract of Pistacia integerrima J. L. Stewart barks and it was also oriented to evaluate the in vivo and in silico anti-inflammatory activity. By NMR and crystallography techniques, we have isolated a triterpenoid identified as daturaolone (compound 1). This compound showed in vivo a significant and dose dependent (1-30 mg/kg) anti-inflammatory activity on carrageenan-induced mouse paw oedema (ED50 = 10.1 mg/kg) and on acetic acid-induced writhing responses in mice (ED50 = 13.8 mg/kg). In the in vivo experiments, the effect of tested compound was also evaluated in presence of the reference drug diclofenac (1-30 mg/kg). Moreover, in silico analysis of receptor ligand complex shows that compound 1 interacts with cyclooxygenases (COXs) binding sites displaying an interesting interaction with COX-1. These findings suggest that compound 1 isolated from P. integerrima possesses in vivo anti-inflammatory and antinociceptive potentials, which are supported in silico by an interaction with COXs receptors.
本研究致力于从笃耨香(Pistacia integerrima J. L. Stewart)树皮的甲醇提取物中分离活性成分,并评估其体内和计算机模拟的抗炎活性。通过核磁共振(NMR)和晶体学技术,我们分离出一种三萜类化合物,鉴定为曼陀罗醇(化合物1)。该化合物在体内对角叉菜胶诱导的小鼠爪肿胀(半数有效剂量[ED50]=10.1mg/kg)和乙酸诱导的小鼠扭体反应(ED50=13.8mg/kg)显示出显著的剂量依赖性(1-30mg/kg)抗炎活性。在体内实验中,还在参考药物双氯芬酸(1-30mg/kg)存在的情况下评估了受试化合物的效果。此外,受体配体复合物的计算机模拟分析表明,化合物1与环氧化酶(COXs)结合位点相互作用,与COX-1表现出有趣的相互作用。这些发现表明,从笃耨香中分离出的化合物1具有体内抗炎和镇痛潜力,计算机模拟显示其与COXs受体相互作用为该潜力提供了支持。