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Chalcone derivatives: synthesis in vitro and in vivo evaluation of their anti-anxiety anti-depression and analgesic effects

机译:查耳酮衍生物:合成体外和体内评估其抗焦虑抗抑郁和镇痛作用

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摘要

Anxiety disorders, depression and pain are highly prevalent pathologies. Their pharmacotherapy is associated with unwanted side effects; hence there is a clinical need to develop more effective drugs with fewer adverse reactions.Chalcones are one of the major classes of naturally occurring compounds. Chalcones and their derivatives have a huge importance in medicinal chemistry, displaying a wide range of pharmacological activities including anti-inflammatory, antimicrobial, antioxidant, cytotoxic and antitumor actions.The aim of this work was to evaluate chalcone effects on different targets involved in these pathologies. We have synthesized a series of simple chalcone derivatives taking common structural requirements described in literature related to their anxiolytic-like, antidepressant-like and/or antinociceptive properties into account.Furthermore, their potential in vitro effects towards different targets involved in these pathologies were evaluated. We have obtained twenty chalcones with moderate to high yields and assessed their ability to bind distinctive receptors, from rat brain homogenates, by displacement of labelled specific ligands: [3H] FNZ (binding site of benzodiazepines/GABAA), [3H] 8-OH-DPAT (serotonin 5-HT1A) and [3H] DAMGO (μ-opioid). Those compounds that showed the better in vitro activities were evaluated in mice using different behavioural tasks. In vivo results showed that 5′-methyl-2′-hydroxychalcone (>9) exerted anxiolytic-like effects in mice in the plus maze test. While chalcone nuclei (>1) revealed antidepressant-like activities in the tail suspension test. In addition, the novel 5′-methyl-2′-hydroxy-3′-nitrochalcone (>12) exhibited antinociceptive activity in acute chemical and thermal nociception tests (writhing and hot plate tests). In conclusion, chalcones are thus promising compounds for the development of novel drugs with central nervous system (CNS) actions.
机译:焦虑症,抑郁症和疼痛是高度流行的病理。他们的药物疗法会带来不良的副作用;因此,临床上需要开发出具有更少不良反应的更有效药物。查尔酮是自然存在的化合物的主要类别之一。查耳酮及其衍生物在药物化学中具有重要意义,显示出广泛的药理活性,包括抗炎,抗微生物,抗氧化剂,细胞毒性和抗肿瘤作用。这项工作的目的是评估查尔酮对这些病理所涉及的不同靶标的作用。 。我们合成了一系列简单的查尔酮衍生物,并考虑到了与它们的抗焦虑样,抗抑郁样和/或抗伤害感受特性相关的文献中描述的常见结构要求,并评估了它们对涉及这些病理学的不同靶标的体外作用的潜力。我们已经从鼠脑匀浆中通过置换标记的特定配体:[ 3 H] FNZ(苯并二氮杂卓/ GABAA的结合位点),从中脑高产动物中获得了二十种查耳酮,并评估了它们结合独特受体的能力。 ),[ 3 H] 8-OH-DPAT(5-羟色胺5-HT1A)和[ 3 H] DAMGO(μ阿片类药物)。在小鼠中使用不同的行为任务对那些表现出更好的体外活性的化合物进行了评估。在体内实验结果表明,在迷宫试验中,5'-甲基-2'-羟基查耳酮(> 9 )对小鼠产生了抗焦虑样作用。查尔酮核(> 1 )在尾部悬浮试验中显示出抗抑郁样活性。此外,新型5'-甲基-2'-羟基-3'-硝基查耳酮(> 12 )在急性化学和热伤害感受试验(扭体和热板试验)中显示出抗伤害感受的活性。总而言之,查耳酮因此是开发具有中枢神经系统(CNS)作用的新药的有前途的化合物。

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