S. barbata D. Don中的Hispidulin的抗抑郁潜力:通过神经化学和行为评估揭示机制。

Arzoo Pannu, Ramesh K Goyal, Shikha Goswami
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引用次数: 0

摘要

背景和目的:本研究旨在探讨Hispidulin的抗抑郁特性,Hispidulin是黄芩中的一种黄酮类化合物。之所以选择Hispidulin,是因为它对黄嘌呤氧化酶(XO)具有显著的抑制活性,而XO是抑郁症病理生理学中的一个参数:采用小鼠慢性不可预测轻度应激(CUMS)模型对小鼠进行为期21天的严格评估,以诱发抑郁症,并采用尾悬试验(TST)、强迫游泳试验(FST)和野外开放试验(OFT)对其抗抑郁特性进行严格评估。丙咪嗪和氟西汀被用作标准药物。此外,还进行了神经化学分析,以量化大脑皮层、海马和下丘脑中的血清素(5-HT)、去甲肾上腺素(NE)和多巴胺(DA)水平。通过估算单胺氧化酶(MAO)活性和评估大脑中的抗氧化酶水平,进一步了解了机理。此外,还测定了血浆中亚硝酸盐和皮质酮的水平,以确定其基本作用机制:结果:Hispidulin具有明显的抗抑郁作用,这体现在TST和FST的不动时间缩短以及OFT的探索行为增加。神经化学分析显示,关键脑区的 5-羟色胺、NE 和 DA 水平得到恢复。此外,Hispidulin 还能调节 MAO 活性,提高大脑中抗氧化酶的水平。血浆亚硝酸盐水平升高,表明一氧化氮合成增强,而皮质酮水平降低:我们的研究结果表明,Hispidulin 可通过影响单胺类神经递质、MAO 活性和抗氧化防御功能发挥强效抗抑郁作用。这些结果为我们深入了解 Hispidulin 的抗抑郁作用提供了宝贵的机理依据,支持其在抑郁症治疗中的潜在应用。
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Antidepressant Potential of Hispidulin Present in S. barbata D. Don: Mechanistic Insights through Neurochemical and Behavioral Assessments.

Background and aim: This study aims to investigate the antidepressant properties of Hispidulin, a flavonoid present in Scutellaria barbata D. Don. The selection of Hispidulin stems from its notable inhibitory activity against Xanthine Oxidase (XO), a parameter in the pathophysiology of depression.

Material and methods: Mice were subjected to a rigorous evaluation using a murine model of Chronic Unpredictable Mild Stress (CUMS) to induce depression for 21 days and antidepressant properties were rigorously assessed using the Tail Suspension Test (TST), Forced Swim Test (FST), and Open Field Test (OFT). Imipramine and fluoxetine were used as standard drugs. Additionally, neurochemical analyses were conducted to quantify serotonin (5-HT), norepinephrine (NE), and dopamine (DA) levels in the cortex, hippocampus, and hypothalamus. Further mechanistic insights were sought through the estimation of monoamine oxidase (MAO) activity and assessment of antioxidant enzyme levels in the brain. Plasma nitrite and corticosterone levels were also measured to delineate the underlying mechanism of action.

Results: Hispidulin demonstrated significant antidepressant effects, as evidenced by reduced immobility time in TST and FST and increased exploratory behavior in OFT. Neurochemical analysis revealed restoration of 5-HT, NE, and DA levels in key brain regions. Furthermore, Hispidulin modulated MAO activity and enhanced antioxidant enzyme levels in the brain. Plasma nitrite levels were elevated, indicating enhanced nitric oxide synthesis, while corticosterone levels were reduced.

Conclusion: Our findings indicate that Hispidulin exerts potent antidepressant effects, potentially mediated through its influence on monoaminergic neurotransmitters, MAO activity, and antioxidant defenses. These results provide valuable mechanistic insights into the antidepressant action of Hispidulin, supporting its potential therapeutic application in depressive disorders.

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