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紫檀精油通过调节神经递质和神经炎症缓解社交挫败应激暴露小鼠的行为损伤。

Essential oil of Pterocarpus santalinus L. alleviates behavioral impairments in social defeat stress-exposed mice by regulating neurotransmission and neuroinflammation.

机构信息

Department of Physiology, Dongguk University College of Korean Medicine, Gyeongju 38066, Republic of Korea; Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Department of Physiology, Dongguk University College of Korean Medicine, Gyeongju 38066, Republic of Korea.

出版信息

Biomed Pharmacother. 2024 Feb;171:116164. doi: 10.1016/j.biopha.2024.116164. Epub 2024 Jan 18.

Abstract

BACKGROUND

Pterocarpus santalinus L. essential oil (PSEO) is traditionally employed for treating fever and mental aberrations. We aim to explore the antidepressant potential of intranasal PSEO in social defeat stress (SDS)-expose mice and identify its mechanisms and components.

METHODS

PSEO components were analyzed using gas chromatography-mass spectrometry (GC-MS). C57BL/6 mice underwent a 10-day SDS with intranasal PSEO (10, 20 mg/kg) for 21 days. Efficacy was evaluated through changes in behaviors and serum corticosterone (CORT), hippocampal neurotransmitter, and inflammatory cytokine levels. In vitro effects were examined using primary hippocampal neurons, PC12 and BV2 cells.

RESULTS

GC-MS identified 22 volatile compounds in PSEO, and (+)-ledene (16.7%), cedrol (13.5%), and isoaromadendrene epoxide (7.0%) as major components. PSEO (20 mg/kg) significantly reversed SDS-induced social withdrawal, increased open-area explorations in the open field test (OFT) and elevated plus maze (EPM) test, and reduced immobility time in the tail suspension test (TST) and forced swimming test (FST). PSEO downregulated serum CORT and hippocampal interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α levels, while increasing hippocampal gamma-aminobutyric acid (GABA), norepinephrine (NE), and serotonin (5-HT) levels. PSEO (0.1, 1, 10 µg/mL) reduced neurotoxicity and neuroinflammation in PC12 and BV2 cells, respectively. PSEO (10 µg/mL) enhanced glutamic acid decarboxylase 6 (GAD6)- and GABA B receptor 1 (GABABR1)-positive puncta in the hippocampal neurons and FM1-43 fluorescence intensity.

CONCLUSION

Intranasal PSEO exhibited antidepressant-like effects on SDS-exposed mice, potentially through modulating stress hormone, neurotransmission, and neuroinflammation. Further investigation into the pharmacokinetics, bioavailability, and mechanisms of (+)-ledene, cedrol, and isoaromadendrene epoxide is needed.

摘要

背景

降香黄檀精油(PSEO)传统上用于治疗发热和精神错乱。我们旨在探索经鼻给予 PSEO 对社交挫败应激(SDS)暴露小鼠的抗抑郁作用,并确定其机制和成分。

方法

使用气相色谱-质谱联用(GC-MS)分析 PSEO 成分。C57BL/6 小鼠接受 10 天 SDS 处理,并经鼻给予 PSEO(10、20mg/kg)21 天。通过行为变化以及血清皮质酮(CORT)、海马神经递质和炎性细胞因子水平来评估疗效。使用原代海马神经元、PC12 和 BV2 细胞进行体外研究。

结果

GC-MS 在 PSEO 中鉴定出 22 种挥发性化合物,其中(+)-葎草烯(16.7%)、雪松醇(13.5%)和异莪术烯环氧化物(7.0%)为主要成分。PSEO(20mg/kg)显著逆转了 SDS 诱导的社会回避,增加了旷场试验(OFT)和高架十字迷宫(EPM)试验中的开阔区域探索,并减少了悬尾试验(TST)和强迫游泳试验(FST)中的不动时间。PSEO 下调了血清 CORT 和海马白细胞介素(IL)-1β、IL-6 和肿瘤坏死因子(TNF)-α水平,同时增加了海马γ-氨基丁酸(GABA)、去甲肾上腺素(NE)和 5-羟色胺(5-HT)水平。PSEO(0.1、1、10μg/mL)分别降低了 PC12 和 BV2 细胞的神经毒性和神经炎症。PSEO(10μg/mL)增强了海马神经元中谷氨酸脱羧酶 6(GAD6)和 GABA B 受体 1(GABABR1)阳性斑点和 FM1-43 荧光强度。

结论

经鼻给予 PSEO 对 SDS 暴露小鼠表现出抗抑郁样作用,可能通过调节应激激素、神经递质和神经炎症。需要进一步研究(+)-葎草烯、雪松醇和异莪术烯环氧化物的药代动力学、生物利用度和机制。

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