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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Lutein prevents corticosterone-induced depressive-like behavior in mice with the involvement of antioxidant and neuroprotective activities
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Lutein prevents corticosterone-induced depressive-like behavior in mice with the involvement of antioxidant and neuroprotective activities

机译:叶黄素通过抗氧化剂和神经保护活动的参与,防止小鼠中的皮质酮诱导的抑郁症状行为

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Depression is a neuropsychiatry medical condition with high prevalence, in which the hypothalamic-pituitary-adrenal axis dysfunction has been postulated as the main cause. The glucocorticoids can be harmful to the brain, particularly by induction of oxidative stress and glutamatergic damage, therefore antioxidants or neuroprotective agents could have beneficial effects. Lutein (LUT) is a dietary xanthophyll able to arrive in the brain that has been used for therapy of macular degeneration. In this sense, several studies pointed beneficial effects of LUT in the brain, particularly in the hippocampus and prefrontal cortex, key regions in mood regulation. Thus, this study sought to evaluate antidepressant-like, antioxidant and neuroprotective effects of LUT (0.1, 1 and 10 mg/kg) and fluoxetine (10 mg/kg) given orally (p.o.), acute, 7 or 21 days, once a day, in combination or not with corticosterone (20 mg/kg) in mice. After behavioral evaluation, the hippocampus, prefrontal cortex, and plasma were collected to assess the oxidative stress markers. And the neuroprotection against glutamate was developed through prefrontal cortex and hippocampal slices. LUT and fluoxetine in acute or subchronic treatment decreased immobility time at the dose 10 mg/kg. Furthermore, corticosterone was effective to induce depressive-like behavior accompanied by an increase of the oxidative stress. Conversely, LUT and fluoxetine were able to counteract the behavioral changes displayed by corticosterone showing antidepressant-like effect. In addition, both LUT and fluoxetine presented antioxidant effect in the hippocampus, prefrontal cortex and plasma of mice, and exhibited a capability to protect hippocampal and prefrontal cortex slices against glutamatergic toxicity. Our results demonstrated that LUT treatment presented an antidepressant-like effect with the involvement of oxidative stress and neurochemical abnormalities amelioration. Therefore, LUT, widely used for therapy of macular degeneration emerge as a promising agent useful in the management of depression.
机译:抑郁症是一种具有高患病率的神经精神病性能,其中丘脑垂体 - 肾上腺轴功能障碍已被假定为主要原因。糖皮质激素可能对大脑有害,特别是通过诱导氧化应激和谷氨酸裂扰损伤,因此抗氧化剂或神经保护剂可具有有益的效果。叶黄素(LUT)是一种能够到达用于治疗黄斑变性的大脑的膳食曲折。从这个意义上讲,几项研究呈现LUT在大脑中的有益作用,特别是在海马和前额叶皮质,情绪调节中的关键区域。因此,本研究寻求评估口服(0.1,10mg / kg)和氟西汀(10mg / kg)给予口服(PO),急性,7或21天的抗抑郁药物,抗氧化剂和神经保护作用,每次a一天,组合与小鼠的皮质酮(20mg / kg)。在行为评估之后,收集海马,前额叶皮质和等离子体以评估氧化应激标记物。通过前额叶皮质和海马切片开发了对谷氨酸的神经保护作用。在急性或次级处理中的LUT和氟苯甲丝在剂量10mg / kg时降低了不动的时间。此外,皮质酮有效地诱导抑制抑制性的行为伴随着氧化应激的增加。相反,LUT和Flyoxetine能够抵消皮质酮显示出抗抑郁药物的皮质酮显示的行为变化。此外,LUT和Flyoxetine均在海马,前额叶皮质和小鼠血浆中呈现抗氧化效果,并表现出一种保护海马和前额叶皮质切片免受谷氨酰胺毒性的能力。我们的结果表明,LUT处理呈现了一种类似氧化胁迫和神经化学异常改善的抗抑郁药物的效果。因此,LUT,广泛用于黄斑变性的治疗出现,作为在抑郁症管理中有用的令人欣赏的剂。

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