a Medical Plants Research Center, Basic Health Sciences Institute , Shahrekord University of Medical Sciences , Shahrekord , Iran.
b Department of Biology , Izeh Branch, Islamic Azad University , Izeh , Iran.
Pharm Biol. 2018 Dec;56(1):672-677. doi: 10.1080/13880209.2018.1543330.
Scopolamine, a muscarinic receptor antagonist, causes memory loss that resembles Alzheimer's disease (AD). Echium amoenum L. (Boraginaceae) is a famous medicinal plant of Iran that is traditionally used as a sedative and mood enhancer.
This study evaluates the effect of hydroalcoholic extract of E. amoenum flowers on scopolamine-induced memory impairment in rats.
Fifty male Wistar rats were randomly divided into five groups. Control group received normal saline, model group received scopolamine (0.7 mg/kg, IP, daily for 21 days), and test groups received E. amoenum extract (50, 75, and 100 mg/kg, IP, daily for 21 days) 30 min before each scopolamine injection. The elevated plus maze (EPM), shuttle box, novel object and rotarod tests were performed after treatment. Brain levels of malondialdehyde (MDA) and total antioxidant capacity (TCA) were also determined.
Scopolamine-treated rats spent more time exploring the novel object compared to the control, and E. amoenum extract at all three doses significantly decreased the time spent exploring the novel object (p < 0.05). E. amoenum extract (75 and 100 mg/kg) significantly elongated the secondary latency in rats receiving scopolamine in the shuttle box test (p < 0.05). In addition, treatment with 75 and 100 mg/kg doses of E. amoenum extract significantly ameliorated scopolamine-induced motor in coordination in rotarod test (p < 0.05). It also significantly increased the time spent in the open arms and reduced the time spent in the closed arms of EPM (p < 0.05). Treatment of scopolamine-exposed rats with E. amoenum extract significantly increased TCA and reduced MDA level of brain (p < 0.05).
E. amoenum extract shows protective effect against scopolamine-induced impairment and is suggested to be tested in clinical trials to evaluate the efficacy on AD.
莨菪碱是一种毒蕈碱受体拮抗剂,可引起类似于阿尔茨海默病(AD)的记忆丧失。天蓝地黄(蓝蓟属)是一种著名的药用植物,伊朗传统上用作镇静剂和情绪增强剂。
本研究评估天蓝地黄花的水醇提取物对大鼠东莨菪碱诱导的记忆障碍的影响。
50 只雄性 Wistar 大鼠随机分为五组。对照组给予生理盐水,模型组给予东莨菪碱(0.7mg/kg,腹腔注射,每日 21 天),实验组给予天蓝地黄提取物(50、75 和 100mg/kg,腹腔注射,每日 21 天),在每次东莨菪碱注射前 30 分钟。治疗后进行高架十字迷宫(EPM)、穿梭箱、新物体和转棒试验。还测定脑丙二醛(MDA)和总抗氧化能力(TCA)水平。
与对照组相比,东莨菪碱处理的大鼠在探索新物体上花费的时间更多,天蓝地黄提取物在所有三种剂量下均显著减少了探索新物体的时间(p<0.05)。天蓝地黄提取物(75 和 100mg/kg)显著延长了穿梭箱试验中接受东莨菪碱的大鼠的次级潜伏期(p<0.05)。此外,75 和 100mg/kg 剂量的天蓝地黄提取物治疗显著改善了东莨菪碱诱导的旋转棒试验中的运动协调(p<0.05)。它还显著增加了在开放臂上花费的时间,并减少了在 EPM 中封闭臂上花费的时间(p<0.05)。天蓝地黄提取物治疗东莨菪碱暴露的大鼠显著增加了脑 TCA 并降低了 MDA 水平(p<0.05)。
天蓝地黄提取物对东莨菪碱诱导的损伤具有保护作用,建议在临床试验中进行测试,以评估其对 AD 的疗效。