摘要
背景:6-chlorotacrine是一种胆碱酯酶抑制剂,在体外表现出比母体化合物他克林更好的抑制潜能,甚至更好。尽管他克林支架广泛用于设计和合成具有抗阿尔茨海默氏病潜力的新化合物,迄今为止还没有研究体内效应。因此,在整个研究过程中进行了基本的毒理学和行为评估。 方法:在BALB / c小鼠和Wistar大鼠中评估最大耐受剂量(MTD)和半数致死剂量(LD50)。在进行多重T迷宫测试,水迷宫测试和逐步被动回避测试的大鼠中观察到行为效应。所有结果与母体化合物 - 他克林的作用进行比较。 结果:与MTD 6.0 / 5.0 mg.kg-1(im,雄性/雌性小鼠),6.0 / 5.0 mg.kg-1(ip,雄性/雌性大鼠)和LD50相比,6-氯代芬明的毒性增加9.0 mg.kg-1(雄性大鼠)。在MTD剂量下,除血浆肌酐水平降低外,未观察到组织病理学变化和血液生化异常。 6-chlorotacrine在逆转奎尼丁基苯甲酸酯诱导的遗忘症方面显示出良好的效果。在水迷宫测试中剂量为1.8 mg.kg-1(20%LD50)时取得了最佳结果;亲认知效应强于他克林(5.2 mg.kg-1,20%LD50)。其他测试剂量(0.9 mg.kg-1和2.7 mg.kg-1)在水迷宫,多重T迷宫和被动回避测试中显示出与他克林类似的效果。 结论:观察到的效果预先确定了6-氯茶碱作为用于合成旨在治疗阿尔茨海默病的新颖多因子药物的有效母体化合物。尽管6-氯代沙林在体内表现出有益的作用并且没有毒性,但是在生物化学和药理学领域的进一步测试对于揭示确切的作用机制,安全性评估和重复给药后化合物的代谢命运是至关重要的
关键词: 阿尔茨海默病,乙酰胆碱酯酶,最大耐受剂量,半数致死量,水迷宫,T迷宫,被动回避。
Current Alzheimer Research
Title:Cholinesterase Inhibitor 6-Chlorotacrine - In Vivo Toxicological Profile and Behavioural Effects
Volume: 15 Issue: 6
关键词: 阿尔茨海默病,乙酰胆碱酯酶,最大耐受剂量,半数致死量,水迷宫,T迷宫,被动回避。
摘要: Background: 6-chlorotacrine is a cholinesterase inhibitor showing good inhibitory potential, even better than parent compound tacrine, in vitro. Despite tacrine scaffold is broadly used for design and synthesis of novel compounds with anti-Alzheimer's potential, no in vivo effects have been investigated so far. Thus, basic toxicological and behavioural evaluation has been carried out throughout this study.
Methods: Maximum tolerated dose (MTD) and median lethal dose (LD50) were assessed in BALB/c mice and Wistar rats. Behavioural effects were observed in rats performing the multiple T-maze test, the water maze test and the step-through passive avoidance test. All outcomes were compared with the effects of parent compound - tacrine.
Results: The toxicity of 6-chlorotacrine was increased compared to tacrine with MTD 6.0/5.0 mg.kg-1 (i.m., male/female mice), 6.0/5.0 mg.kg-1 (i.p., male/female rats) and LD50 9.0 mg.kg-1 (male rats). At MTD doses, no histopathological changes and blood biochemistry abnormalities were observed except decreased plasma creatinine levels. 6-chlorotacrine showed good effects in the reversal of quinuclidinyl benzilate-induced amnesia. Best results were achieved at the dose of 1.8 mg.kg-1 (20% LD50) in the water maze test; the pro-cognitive effect was stronger than that of tacrine (5.2 mg.kg-1, 20% LD50). Other doses tested (0.9 mg.kg-1 and 2.7 mg.kg-1) showed similar effects as tacrine in the water maze, multiple T-maze and passive avoidance test.
Conclusion: Observed effects predetermined 6-chlorotacrine as a potent parent compound for the synthesis of novel multifactorial drugs intended to the treatment of Alzheimer's disease. Even though 6- chlorotacrine showed in vivo beneficial effect with no signs of toxicity, further tests on the field of biochemistry and pharmacology are essential to disclose the exact mechanism of action, safety evaluation and the metabolic fate of the compound after the repeated administration.
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Cite this article as:
Cholinesterase Inhibitor 6-Chlorotacrine - In Vivo Toxicological Profile and Behavioural Effects, Current Alzheimer Research 2018; 15 (6) . https://dx.doi.org/10.2174/1567205015666171212105412
DOI https://dx.doi.org/10.2174/1567205015666171212105412 |
Print ISSN 1567-2050 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5828 |
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