Unité de Pharmacognosie/Biologie Moléculaire 99/UR/07-03. Faculté de Pharmacie de Monastir, Rue Avicenne 5000 Monastir, Tunisia.
J Appl Toxicol. 2010 Aug;30(6):551-8. doi: 10.1002/jat.1525.
Antioxidant activity of isorhamnetin 3-O-neohesperidoside, isolated from the leaves of Acacia salicina, was determined by the ability of this compound to inhibit xanthine oxidase activity and to scavenge the free radical 2,2'-azino-bis (3-ethylbenzthiazoline-6-sulfonic acid) (ABTS(.-)) diammonium salt. Antigenotoxic activity was assessed using the SOS chromotest assay. This compound has the ability to scavenge the ABTS(.+) radical by a hydrogen donating mechanism. We also envisaged the study of the antioxidant effect of this compound by the enzymatic xanthine/xanthine oxidase (X/XOD) assay. Results indicated that isorhamnetin 3-O-neohesperidoside was a potent inhibitor of xanthine oxidase and superoxide anion scavengers. Moreover, this compound induced an inhibitory activity against nifuroxazide and aflatoxine B1 (AFB1) induced genotoxicity. Taken together, these observations provide evidence that isorhamnetin 3-O-neohesperidoside isolated from the leaves of A. salicina is able to protect cells against the consequences of oxidative stress.
从相思树叶子中分离得到的异鼠李素 3-O-新橙皮苷的抗氧化活性,是通过该化合物抑制黄嘌呤氧化酶活性和清除自由基 2,2'-偶氮-双(3-乙基苯并噻唑啉-6-磺酸)二铵盐(ABTS(.-))的能力来确定的。抗原毒性活性使用 SOS 显色试验进行评估。该化合物具有通过供氢机制清除 ABTS(+)自由基的能力。我们还设想通过酶促黄嘌呤/黄嘌呤氧化酶(X/XOD)试验研究该化合物的抗氧化作用。结果表明,异鼠李素 3-O-新橙皮苷是黄嘌呤氧化酶和超氧阴离子的有效抑制剂。此外,该化合物还能抑制硝呋妥因和黄曲霉毒素 B1(AFB1)诱导的遗传毒性。综上所述,这些观察结果表明,从相思树叶子中分离得到的异鼠李素 3-O-新橙皮苷能够保护细胞免受氧化应激的影响。