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甘草酸通过 GLT1 和 Per1/2 依赖的途径改善焦虑样行为。

Glycyrrhizic acid treatment ameliorates anxiety-like behaviour via GLT1 and Per1/2-dependent pathways.

机构信息

Department of Pharmacy, Xijing Hospital, Air Force Medical University, 710032, Xi'an, Shaanxi, PR China.

Departments of Ultrasound, The First Affiliated Hospital of Xi'an Jiaotong University, 710061, Xi'an, Shaanxi, PR China.

出版信息

J Ethnopharmacol. 2024 Jun 28;328:118013. doi: 10.1016/j.jep.2024.118013. Epub 2024 Mar 5.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

As a traditional Chinese medicinal herb, Glycyrrhiza.

URALENSIS

Fisch. (licorice root, chinese name: Gancao) has a variety of medicinal values and is widely used clinically. Its main active ingredient, glycyrrhizic acid (GA), is believed to have a neuroprotective effect. However, the underlying biological mechanisms of GA on stress-induced anxiety disorders are still unclear.

AIM OF THE STUDY

To investigate the anti-anxiety effect of GA and its underlying mechanism.

METHODS

We selected the anxiety model induced by repeated chronic restraint stress (CRS) for 2 h on each of 7 consecutive days. GA (4, 20, 100 mg/kg) was injected intraperitoneally once daily for 1 week. The potential GA receptors were identified using whole-cell patches and computer-assisted docking of molecules. High-throughput RNA sequencing, adeno-associated virus-mediated gene regulation, Western blotting, and RT-qPCR were used to assess the underlying molecular pathways.

RESULTS

GA alleviate depression-like and anxiety-like behaviors in CRS mice. GA decreased synaptic transmission by facilitating glutamate reuptaking in mPFC. Meanwhile, long-term GA treatment increased the expression of clock genes Per1 and Per2. Suppressing both Per1 and Per2 abolished the anxiolytic effects of GA treatment.

CONCLUSION

Our study suggests that GA may be developed for the treatment of stress-induced anxiety disorders, and its mechanism is related to GLT1 and Per1/2-dependent pathways. This presents a novel approach to discovering potent therapeutic drugs.

摘要

民族药理学相关性

作为一种传统的中药,甘草(licorice root,中文名:甘草)具有多种药用价值,在临床上广泛应用。其主要活性成分甘草酸(GA)被认为具有神经保护作用。然而,GA 对应激诱导的焦虑障碍的潜在生物学机制尚不清楚。

研究目的

探讨 GA 的抗焦虑作用及其潜在机制。

方法

我们选择了重复慢性束缚应激(CRS)诱导的焦虑模型,在连续 7 天的每天 2 小时内进行。GA(4、20、100mg/kg)每天腹腔注射一次,持续 1 周。使用全细胞膜片钳和计算机辅助分子对接鉴定潜在的 GA 受体。高通量 RNA 测序、腺相关病毒介导的基因调控、Western blot 和 RT-qPCR 用于评估潜在的分子途径。

结果

GA 缓解 CRS 小鼠的抑郁样和焦虑样行为。GA 通过促进 mPFC 中的谷氨酸再摄取来减少突触传递。同时,长期 GA 处理增加了时钟基因 Per1 和 Per2 的表达。抑制 Per1 和 Per2 均可消除 GA 处理的抗焦虑作用。

结论

我们的研究表明,GA 可能被开发用于治疗应激诱导的焦虑障碍,其机制与 GLT1 和 Per1/2 依赖性途径有关。这为发现有效的治疗药物提供了一种新方法。

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