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达玛烷型甾体皂苷元通过上调 ERK/CREB/BDNF 通路来减轻应激诱导的焦虑样行为。

Dammarane sapogenins attenuates stress-induced anxiety-like behaviors by upregulating ERK/CREB/BDNF pathways.

机构信息

Research Center for Pharmacology and Toxicology, Institute of Medicinal Plant Development (IMPLAD), Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Affiliated TCM Hospital/School of Pharmacy/Sino-Portugal TCM International Cooperation Center, Southwest Medical University, Luzhou, China.

出版信息

Phytother Res. 2020 Oct;34(10):2721-2729. doi: 10.1002/ptr.6713. Epub 2020 May 19.

DOI:10.1002/ptr.6713
PMID:32431006
Abstract

Dammarane sapogenins (DS), an extract derived from ginseng by alkaline hydrolysis of total ginsenosides, possesses high pharmacological activity and higher bioavailability than ginsenosides. The present study was designed to investigate the anxiolytic-like effects of DS in a mouse model of chronic social defeat stress (CSDS). DS (40 and 80 mg/kg) significantly ameliorated social avoidance and anxiety-like behavior in four test models of CSDS, showing increased time in the interaction zone in the social interaction test and in the center of the field in the open field test, an increased percentage of entries and open arm time in the elevated plus maze, and reduced latency to eat in the novelty-suppressed feeding test. Biochemical analyses showed that DS significantly reduced serum corticosterone levels and increased brain concentration of neurotransmitter 5-HT and noradrenaline in CSDS mice. Treatment with DS significantly upregulated BDNF (brain-derived neurotrophic factor), p-CREB/CREB and p-ERK1/2/ERK1/2 protein expression in the hippocampus and prefrontal cortex of CSDS mice. Collectively, these results suggest that DS exerts anxiolytic-like effects in CSDS model mice and the action is mediated, at least in part, by modulating the HPA (hypothalamic-pituitary-adrenal) axis and monoamine neurotransmitter levels, and via ERK/CREB/BDNF signaling pathway.

摘要

达玛烷型人参皂苷(DS)是从总皂苷经碱性水解提取的人参提取物,具有较高的药理活性和生物利用度。本研究旨在探讨 DS 在慢性社会挫败应激(CSDS)小鼠模型中的抗焦虑样作用。DS(40 和 80mg/kg)显著改善了 CSDS 的四种测试模型中的社交回避和焦虑样行为,在社交互动测试中增加了互动区的时间,在开阔场测试中增加了中央区的时间,在高架十字迷宫中增加了进入次数和开放臂时间的百分比,并减少了新奇抑制进食测试中的潜伏期。生化分析表明,DS 可显著降低 CSDS 小鼠的血清皮质酮水平,并增加大脑中神经递质 5-HT 和去甲肾上腺素的浓度。DS 治疗可显著上调 CSDS 小鼠海马和前额叶皮质中的 BDNF(脑源性神经营养因子)、p-CREB/CREB 和 p-ERK1/2/ERK1/2 蛋白表达。综上所述,这些结果表明 DS 在 CSDS 模型小鼠中具有抗焦虑样作用,其作用至少部分通过调节 HPA(下丘脑-垂体-肾上腺)轴和单胺神经递质水平以及通过 ERK/CREB/BDNF 信号通路来介导。

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