首页> 美国卫生研究院文献>Toxicology Reports >Anticholinergic and antioxidant activities of usnic acid-an activity-structure insight
【2h】

Anticholinergic and antioxidant activities of usnic acid-an activity-structure insight

机译:松萝酸的抗胆碱能和抗氧化活性-活性结构的见解

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Usnic acid, as active dibenzofuran derivative, isolated and characterized from some lichen species. The aim of manuscript was to evaluate antioxidant, anticholinergic and antidiabetic potentials of usnic acid as an important natural product. Antioxidant profile of usnic acid determined by eight distinguishes bioanalytical antioxidant methods including 1,1-diphenyl-2-picrylhydrazyl (DPPH·), 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS ), superoxide anion radical (O ) and N,N-dimethyl-p-phenylenediamine (DMPD ) scavenging activities, cupric ion (Cu ), ferric ion (Fe ) and Fe -TPTZ reducing abilities and ferrous ion (Fe ) chelating activity. Usnic acid was found as potent DPPH· (IC : 49.50 μg/mL), DMPD (IC : 33.00 μg/mL), O (IC : 18.68 μg/mL), and ABTS (IC : 10.41 μg/mL) scavenging effects. Also, the inhibition effects of usnic acid were tested against some metabolic enzymes including acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) linked to neurodegenerative diseases. Both enzymes play important roles in cholinergic transmission by hydrolyzing the neurotransmitter acetylcholine in cholinergic synapses, central nervous system, neuromuscular junctions and autonomic ganglia. Their inhibitors were used for clinical treatment of some neurodegenerative conditions including myasthenia gravis, Alzheimer's disease, apathy, glaucoma, postural tachycardia syndrome and dementia. Furthermore, usnic acid showed the potent inhibition profiles against AChE (IC : 1.273 nM) and BChE (IC : 0.239 nM) enzymes. The results clearly showed that usnic acid is an important natural product with antioxidant and anticholinergic potentials.
机译:松萝酸作为活性二苯并呋喃衍生物,是从某些地衣物种中分离并鉴定的。手稿的目的是评估松香酸作为一种重要的天然产物的抗氧化,抗胆碱能和抗糖尿病的潜力。通过八种不同的生物分析抗氧化剂方法确定了松萝酸的抗氧化特性,其中包括1,1-二苯基-2-吡啶并肼(DPPH·),2,2'-叠氮基双(3-乙基苯并噻唑啉-6-磺酸)(ABTS),超氧化物阴离子自由基(O)和N,N-二甲基对苯二胺(DMPD)的清除活性,铜离子(Cu),铁离子(Fe)和Fe -TPTZ的还原能力以及亚铁离子(Fe)的螯合活性。发现松萝酸作为有效的DPPH·(IC:49.50μg/ mL),DMPD(IC:33.00μg/ mL),O(IC:18.68μg/ mL)和ABTS(IC:10.41μg/ mL)清除作用。此外,测试了松萝酸对与神经退行性疾病有关的一些代谢酶(包括乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BChE))的抑制作用。两种酶通过水解胆碱能突触,中枢神经系统,神经肌肉接头和植物神经节中的神经递质乙酰胆碱,在胆碱能传递中起重要作用。他们的抑制剂被用于一些神经退行性疾病的临床治疗,包括重症肌无力,阿尔茨海默氏病,冷漠,青光眼,姿势性心动过速综合征和痴呆。此外,松萝酸显示出对AChE(IC:1.273 nM)和BChE(IC:0.239 nM)酶的有效抑制作用。结果清楚地表明,松萝酸是具有抗氧化剂和抗胆碱能潜能的重要天然产物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号