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Anxiolytic- and antidepressant-like effects of Silymarin compared to diazepam and fluoxetine in a mouse model of mild traumatic brain injury

机译:轻度创伤性脑损伤小鼠模型中,西米林和氟西汀相比,西米林和氟西汀的抗焦育和抗抑郁药物

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摘要

Abstract Clinical and experimental studies have shown that mild traumatic brain injury (mTBI) is associated with increased anxiety- and depression-related behaviors and inflammation in the brain. Unfortunately, there are no specific therapies for long-term behavioral consequences of mTBI. This study set out to determine whether silymarin treatment compared to diazepam (DZP) and fluoxetine (FLX) can reduce neuroinflammation, anxiety- and depression-like behaviors after mTBI induction in mice. We used open field, elevated plus maze, light-dark box, zero maze, sucrose preference, forced swim, and tail suspension tests to assess anxiety and depression-like behaviors in mTBI-induced mice. The levels of tumor necrosis factor (TNF)-α protein, a marker of inflammation, in the prefrontal cortex and hippocampus was also measured. This study identified that the long-term treatment with DZP, FLX or SIL results in decreased anxiety and depression-like behaviors in mTBI-induced mice. The results also showed that these drugs reduced TNF-α levels in the prefrontal cortex and hippocampus. In addition, there were no significant differences between the effects of SIL and DZP or SIL and FLX on behavioral and cytokine levels in mTBI-induced mice. Our findings support the idea that mTBI could be a risk factor for anxiety- and depression-related disorders and neuroinflammation in the brain. Taken together, this study demonstrates that DZP, FLX or SIL can significantly reduce anxiety- and depression-like symptoms, and neuroinflammation after mTBI induction in mice. Highlights ? Diazepam and Silymarin reduced anxiety-like behavior in mTBI-induced mice. ? Fluoxetine and Silymarin decreased depression-like behavior in mTBI-induced mice. ? Diazepam and Silymarin reduced TNF-α in the prefrontal cortex of mTBI-induced mice. ? Fluoxetine and Silymarin decreased TNF-α in the hippocampus of mTBI-induced mice. ? There were no significant differences between Silymarin and Diazepam or Fluoxetine.
机译:摘要临床和实验研究表明,轻度创伤性脑损伤(MTBI)与脑内焦虑和抑郁相关的行为和脑内炎症有关。不幸的是,MTBI的长期行为后果没有特定的疗法。本研究阐述了与Diazepam(DZP)和氟西汀(FLX)相比的西米林治疗是否可以减少小鼠MTBI诱导后的神经炎症,焦虑和抑郁样行为。我们使用了开放的领域,高迷宫,浅暗盒,零迷宫,蔗糖偏好,强制游泳和尾悬架试验,以评估MTBI诱导的小鼠中的焦虑和抑郁样行为。还测量了肿瘤坏死因子(TNF)-α蛋白,炎症的标志物,在前额叶皮质和海马中的水平。该研究确定,使用DZP,FLX或SIL的长期治疗导致MTBI诱导的小鼠中的焦虑和抑郁样行为降低。结果还表明,这些药物在前额叶皮质和海马中降低了TNF-α水平。此外,SIL和DZP或SIL和FLX对MTBI诱导的小鼠的行为和细胞因子水平之间没有显着差异。我们的调查结果支持MTBI可能成为焦虑和抑郁相关疾病和大脑中神经炎症的危险因素。综合,本研究表明,DZP,FLX或SIL可以显着降低焦虑和抑郁状症状,并在小鼠中MTBI诱导后的神经炎症。强调 ? Diazepam和Silymarin降低了MTBI诱导的小鼠的焦虑性行为。还氟西汀和甲硅烷林在MTBI诱导的小鼠中降低了抑郁症状的行为。还Diazepam和Silymarin在MTBI诱导的小鼠的前额叶皮质中降低TNF-α。还氟西汀和西里马林在MTBI诱导的小鼠的海马中降低了TNF-α。还体米林和二聚醇泮或氟西汀之间没有显着差异。

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