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叶酸作为锂治疗辅助药物对躁狂样行为、氧化应激和炎症参数的疗效在躁狂动物模型中的研究。

Efficacy of folic acid as an adjunct to lithium therapy on manic-like behaviors, oxidative stress and inflammatory parameters in an animal model of mania.

机构信息

Translational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.

Queensland Brain Institute, The Universty of Queensland, St Lucia, QLD, 4072, Australia.

出版信息

Metab Brain Dis. 2020 Feb;35(2):413-425. doi: 10.1007/s11011-019-00503-3. Epub 2019 Dec 15.

DOI:10.1007/s11011-019-00503-3
PMID:31840201
Abstract

Evaluate the efficacy of folic acid (FA) as a therapeutic adjunct to lithium (Li) on the manic-like behaviors as well as parameters of oxidative stress and inflammation in an animal model of mania induced by m-amphetamine (m-AMPH). Wistar rats first received m-AMPH or saline (NaCl 0.9%, Sal) for 14 days. Between the 8th and 14th day, rats were treated with water, Li, FA or a combination of thereof drugs (Li + FA). Manic-like behaviors were assessed in the open-field test. Oxidative stress and inflammation parameters were assessed in the frontal cortex, striatum, and hippocampus. Administration of m-AMPH in rats significantly enhanced the exploratory and locomotor behaviors, as well as the risk-taking and stereotypic behaviors. Li + FA reversed these behavioral alterations elicited by m-AMPH. Administration of this psychostimulant also increased oxidative damage to lipids and proteins, whereas Li + FA reversed these oxidative damages. m-AMPH also induced an increase in the glutathione peroxidase (GPx) activity and a decrease in the glutathione reductase (GR) activity. Li + FA reversed the alteration in GR activity, but not in GPx activity. In addition, m-AMPH increased the IL-1β and TNF-α levels in the rat brain; Li + FA combined therapy reversed the alterations on these inflammatory parameters. FA administration per se reduced the increased TNF-α content induced by m-AMPH. Present study provides evidence that FA is effective as an adjunct to Li standard therapy on manic-like behaviors, oxidative stress and inflammatory parameters in a model of mania induced by m-AMPH.

摘要

评估叶酸 (FA) 作为锂 (Li) 的治疗辅助剂对安非他命 (m-AMPH) 诱导的躁狂动物模型中躁狂样行为以及氧化应激和炎症参数的疗效。Wistar 大鼠首先接受 m-AMPH 或生理盐水 (NaCl 0.9%,Sal) 14 天。在第 8 天和第 14 天之间,大鼠接受水、Li、FA 或两者联合用药 (Li+FA)。在旷场试验中评估躁狂样行为。在额叶皮层、纹状体和海马体中评估氧化应激和炎症参数。在大鼠中给予 m-AMPH 可显著增强探索和运动行为,以及冒险和刻板行为。Li+FA 逆转了 m-AMPH 引起的这些行为改变。给予这种精神兴奋剂还会增加脂质和蛋白质的氧化损伤,而 Li+FA 则逆转了这些氧化损伤。m-AMPH 还诱导谷胱甘肽过氧化物酶 (GPx) 活性增加和谷胱甘肽还原酶 (GR) 活性降低。Li+FA 逆转了 GR 活性的改变,但没有逆转 GPx 活性的改变。此外,m-AMPH 增加了大鼠大脑中的白细胞介素-1β (IL-1β) 和肿瘤坏死因子-α (TNF-α) 水平;Li+FA 联合治疗逆转了这些炎症参数的改变。FA 给药本身可降低 m-AMPH 引起的 TNF-α 含量增加。本研究提供了证据表明,FA 作为 Li 标准治疗的辅助治疗,可有效治疗 m-AMPH 诱导的躁狂模型中的躁狂样行为、氧化应激和炎症参数。

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Interplay Between Amphetamine and Activity Level in Gene Networks of the Mouse Striatum.
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Effect of blueberry extract on energetic metabolism, levels of brain-derived neurotrophic factor, and Ca-ATPase activity in the hippocampus and cerebral cortex of rats submitted to ketamine-induced mania-like behavior.蓝莓提取物对氯胺酮诱导的似躁狂行为大鼠能量代谢、海马和大脑皮层脑源性神经营养因子水平及 Ca-ATP 酶活性的影响。
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