通过姜黄素和载有右大麻酚的固体脂质纳米粒的抗抑郁活性靶向内源性大麻素/CB1受体系统治疗重度抑郁症

Targeting the Endocannabinoid/CB1 Receptor System For Treating Major Depression Through Antidepressant Activities of Curcumin and Dexanabinol-Loaded Solid Lipid Nanoparticles.

作者信息

He Xiaolie, Yang Li, Wang Mei, Zhuang Xizhen, Huang Ruiqi, Zhu Rongrong, Wang Shilong

出版信息

Cell Physiol Biochem. 2017;42(6):2281-2294. doi: 10.1159/000480001. Epub 2017 Aug 17.

Abstract

BACKGROUND/AIMS: This study investigated the underlying mechanisms of the antidepressant effects of curcumin and dexanabinol-loaded solid lipid nanoparticles in corticosterone-induced cell and mice depression models.

METHODS

Curcumin and dexanabinol-loaded solid lipid nanoparticles (Cur/SLNs-HU-211) were synthesized via an emulsifcation and low-temperature solidification method. Antidepressant activities of nanoparticles in a corticosterone-induced major depression model were investigated by MTT assay, cellular uptake by flow cytometry, behaviour by Forced Swimming Test and rotarod test, neurotransmitters by High Performance Liquid Chromatography, Western blotting, qPCR and immunofluorescence.

RESULTS

Treatment with Cur/SLNs-HU-211 induced greater dopamine (DA)/5-hydroxytryptamine (5-HT) release with reduced corticosterone-induced apoptotic cell death in PC12 cells. Additionally, in vivo Cur/SLNs-HU-211 significantly induced recovery from depressive behaviour with increased DA/5-HT levels, CB1 mRNA levels and CB1, p-MEK1 and p-ERK1/2 protein expression levels in the hippocampus and striatum. Cur/SLNs-HU-211 improved CB1 expression and inspired the proliferation of astrocytes in the hippocampus and striatum, exerted neuroprotective effects by preventing corticosterone -induced BDNF/NeuN expression reduction.

CONCLUSION

Our study implies that Cur/SLNs-HU-211 may be a useful approach for treatment of major depression.

摘要

背景/目的:本研究探讨了姜黄素和载有右大麻酚的固体脂质纳米粒在皮质酮诱导的细胞和小鼠抑郁模型中的抗抑郁作用潜在机制。

方法

通过乳化和低温固化法合成了姜黄素和载有右大麻酚的固体脂质纳米粒(Cur/SLNs-HU-211)。采用MTT法研究纳米粒在皮质酮诱导的重度抑郁模型中的抗抑郁活性,通过流式细胞术检测细胞摄取情况,通过强迫游泳试验和转棒试验检测行为,通过高效液相色谱、蛋白质印迹法、定量聚合酶链反应和免疫荧光检测神经递质。

结果

Cur/SLNs-HU-211处理可诱导PC12细胞释放更多多巴胺(DA)/5-羟色胺(5-HT),并减少皮质酮诱导的凋亡细胞死亡。此外,在体内,Cur/SLNs-HU-211显著诱导抑郁行为恢复,海马体和纹状体中DA/5-HT水平、CB1 mRNA水平以及CB1、p-MEK1和p-ERK1/2蛋白表达水平升高。Cur/SLNs-HU-211改善了海马体和纹状体中CB1的表达,并促进了星形胶质细胞的增殖,通过防止皮质酮诱导的脑源性神经营养因子/神经元核抗原(BDNF/NeuN)表达降低发挥神经保护作用。

结论

我们的研究表明,Cur/SLNs-HU-211可能是治疗重度抑郁的一种有效方法。

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