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荠菜籽精油(AHSO),含有天然 α-亚麻酸、硬脂酸、肉豆蔻酸和 β-谷甾醇,能促进神经干细胞的体外增殖和分化。

Alyssum homolocarpum seed oil (AHSO), containing natural alpha linolenic acid, stearic acid, myristic acid and β-sitosterol, increases proliferation and differentiation of neural stem cells in vitro.

机构信息

Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.

Medicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.

出版信息

BMC Complement Altern Med. 2019 Jun 3;19(1):113. doi: 10.1186/s12906-019-2518-4.

DOI:10.1186/s12906-019-2518-4
PMID:31159797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6547481/
Abstract

BACKGROUND

Embryonic neural stem cells (eNSCs) are immature precursors of the central nervous system (CNS), with self-renewal and multipotential differentiation capacities. These are regulated by endogenous and exogenous factors such as alpha-linolenic acid (ALA), a plant-based essential omega-3 polyunsaturated fatty acid.

METHODS

In this study, we investigated the effects of various concentrations of Alyssum homolocarpum seed oil (AHSO), containing natural ALA, stearic acid (SA), myristic acid (MA), and β-sitosterol, on proliferation and differentiation of eNSCs, in comparison to controls and to synthetic pure ALA.

RESULTS

Treatment with natural AHSO (25 to 75 μM), similar to synthetic ALA, caused a significant ~ 2-fold increase in eNCSs viability, in comparison to controls. To confirm this proliferative activity, treatment of NSCs with 50 or 75 μM AHSO resulted in a significant increase in mRNA levels of notch1, hes-1 and Ki-67and NICD protein expression, in comparison to controls. Moreover, AHSO administration significantly increased the differentiation of eNSCs toward astrocytes (GFAP+) and oligodendrocytes (MBP+) in a dose dependent manner and was more potent than ALA, at similar concentrations, in comparison to controls. Indeed, only high concentrations of 100 μM AHSO, but not ALA, caused a significant increase in the frequency of neurons (β-III Tubulin+).

CONCLUSION

Our data demonstrated that AHSO, a rich source of ALA containing also other beneficial fatty acids, increased the proliferation and stimulated the differentiation of eNSCs. We suggest that AHSO's effects are caused by β-sitosterol, SA and MA, present within this oil. AHSO could be used in diet to prevent neurodevelopmental syndromes, cognitive decline during aging, and various psychiatric disorders.

摘要

背景

胚胎神经干细胞(eNSC)是中枢神经系统(CNS)的未成熟前体细胞,具有自我更新和多能分化能力。这些能力受到内源性和外源性因素的调节,如α-亚麻酸(ALA),一种植物源性必需的ω-3 多不饱和脂肪酸。

方法

在这项研究中,我们研究了不同浓度的 Alyssum homolocarpum 籽油(AHSO)对 eNSC 增殖和分化的影响,AHSO 中含有天然 ALA、硬脂酸(SA)、肉豆蔻酸(MA)和β-谷甾醇,与对照组和合成纯 ALA 进行了比较。

结果

与对照组相比,天然 AHSO(25 至 75μM)处理类似于合成 ALA,导致 eNCSs 活力显著增加约 2 倍。为了证实这种增殖活性,用 50 或 75μM AHSO 处理 NSCs 导致 notch1、hes-1 和 Ki-67 的 mRNA 水平以及 NICD 蛋白表达显著增加,与对照组相比。此外,AHSO 给药以剂量依赖的方式显著增加 eNSC 向星形胶质细胞(GFAP+)和少突胶质细胞(MBP+)的分化,并且在相似浓度下比 ALA 更有效,与对照组相比。事实上,只有高浓度的 100μM AHSO,但不是 ALA,导致神经元(β-III Tubulin+)的频率显著增加。

结论

我们的数据表明,AHSO 是 ALA 的丰富来源,还含有其他有益的脂肪酸,可增加 eNSC 的增殖并刺激其分化。我们认为 AHSO 的作用是由存在于这种油中的β-谷甾醇、SA 和 MA 引起的。AHSO 可用于饮食中,以预防神经发育综合征、衰老过程中的认知能力下降和各种精神疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/0ba1c2a6d4a2/12906_2019_2518_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/5df82e44fb7e/12906_2019_2518_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/87d72057f256/12906_2019_2518_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/793e9868ae1e/12906_2019_2518_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/20e35e7cc471/12906_2019_2518_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/0665dcd8d614/12906_2019_2518_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/0ba1c2a6d4a2/12906_2019_2518_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/5df82e44fb7e/12906_2019_2518_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/87d72057f256/12906_2019_2518_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/793e9868ae1e/12906_2019_2518_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/20e35e7cc471/12906_2019_2518_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/0665dcd8d614/12906_2019_2518_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfab/6547481/0ba1c2a6d4a2/12906_2019_2518_Fig6_HTML.jpg

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