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发酵栽培野山参根提取物对小鼠的神经保护作用和抗氧化活性。

Neuroprotective Effect and Antioxidant Potency of Fermented Cultured Wild Ginseng Root Extracts of C.A. Meyer in Mice.

机构信息

Research Institute of Biotechnology, HwajinBioCosmetics CO., LTD, Chuncheon 24232, Korea.

Korea Conformity Laboratories, Yeonsu, Incheon 21999, Korea.

出版信息

Molecules. 2021 May 18;26(10):3001. doi: 10.3390/molecules26103001.

DOI:10.3390/molecules26103001
PMID:34070099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8158381/
Abstract

Wild ginseng has better pharmacological effects than cultivated ginseng. However, its industrialization is limited by the inability to grow wild ginseng on a large scale. Herein, we demonstrate how to optimize ginseng production through cultivation, and how to enhance the concentrations of specific ginsenosides through fermentation. In the study, we also evaluated the ability of fermented cultured wild ginseng root extract (HLJG0701-β) to inhibit acetylcholinesterase (AChE), as well as its neuroprotective effects and antioxidant activity. In tests, HLJG0701-β inhibited AChE activity and exerted neuroprotective and antioxidant effects (showing increased catalyst activity but decreased reactive oxygen species concentration). In tests, after HLJG0701-β was orally administered at doses of 0, 125, 250, and 500 mg/kg in an animal model of memory impairment, behavioral evaluation (Morris water maze test and Y-maze task test) was performed. The levels of AChE, acetylcholine (ACh), blood catalase (CAT), and malondialdehyde (MDA) in brain tissues were measured. The results showed that HLJG0701-β produced the best results at a dose of 250 mg/kg or more. The neuroprotective mechanism of HLJG0701-β was determined to involve the inhibition of AChE activity and a decrease in oxidative stress. In summary, both and tests confirmed that HJG0701-β administration can lead to memory improvement.

摘要

野生人参比栽培人参具有更好的药理作用。然而,由于无法大规模种植野生人参,其产业化受到限制。在此,我们展示了如何通过栽培来优化人参的产量,以及如何通过发酵来提高特定人参皂甙的浓度。在研究中,我们还评估了发酵栽培野山参根提取物(HLJG0701-β)抑制乙酰胆碱酯酶(AChE)的能力,以及其神经保护作用和抗氧化活性。在测试中,HLJG0701-β抑制 AChE 活性,并发挥神经保护和抗氧化作用(表现为催化剂活性增加,而活性氧浓度降低)。在测试中,在记忆障碍动物模型中,HLJG0701-β 以 0、125、250 和 500mg/kg 的剂量口服给药后,进行行为评估(Morris 水迷宫测试和 Y 迷宫任务测试)。测量脑组织中乙酰胆碱酯酶(AChE)、乙酰胆碱(ACh)、血液过氧化氢酶(CAT)和丙二醛(MDA)的水平。结果表明,HLJG0701-β 在 250mg/kg 或更高剂量下效果最佳。HLJG0701-β 的神经保护机制被确定为抑制 AChE 活性和降低氧化应激。总之,和测试都证实了 HJG0701-β 给药可以导致记忆改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/929c8794c28c/molecules-26-03001-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/810dffe9b04b/molecules-26-03001-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/135636046080/molecules-26-03001-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/66b699210506/molecules-26-03001-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/6b1ad40a4225/molecules-26-03001-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/8da0d9b0886b/molecules-26-03001-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/77e641ea45ab/molecules-26-03001-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/d222aa2e17c2/molecules-26-03001-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/820ecfc308e4/molecules-26-03001-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/d0894206f4f8/molecules-26-03001-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/929c8794c28c/molecules-26-03001-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/810dffe9b04b/molecules-26-03001-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/135636046080/molecules-26-03001-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/66b699210506/molecules-26-03001-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/6b1ad40a4225/molecules-26-03001-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/8da0d9b0886b/molecules-26-03001-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/77e641ea45ab/molecules-26-03001-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/d222aa2e17c2/molecules-26-03001-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/820ecfc308e4/molecules-26-03001-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/d0894206f4f8/molecules-26-03001-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a7/8158381/929c8794c28c/molecules-26-03001-g010.jpg

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