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Prophylactic role of Korean red ginseng in astrocytic mitochondrial biogenesis through HIF-1αopen access

Authors
Park, JinhongLee, MinjaeKim, MinsuMoon, SunhongKim, SwungheeKim, SueunKoh, Seong-HoKim, Young -MyeongChoi, Yoon Kyung
Issue Date
May-2022
Publisher
고려인삼학회
Keywords
Korean Red Ginseng; Astrocytic mitochondria biogenesis; Hypoxia-inducible factor-1 alpha; Angiogenesis; Neural stem cell differentiation
Citation
Journal of Ginseng Research, v.46, no.3, pp 408 - 417
Pages
10
Indexed
SCIE
SCOPUS
KCI
Journal Title
Journal of Ginseng Research
Volume
46
Number
3
Start Page
408
End Page
417
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/138735
DOI
10.1016/j.jgr.2021.07.003
ISSN
1226-8453
2093-4947
Abstract
Background: Korean Red Ginseng extract (KRGE) has been used as a health supplement and herbal medicine. Astrocytes are one of the key cells in the central nervous system (CNS) and have bioenergetic potential as they stimulate mitochondrial biogenesis. They play a critical role in connecting the brain vasculature and nerves in the CNS. Methods: Brain samples from KRGE-administered mice were tested using immunohistochemistry. Treatment of human brain astrocytes with KRGE was subjected to assays such as proliferation, cytotoxicity, Mitotracker, ATP production, and O-2 consumption rate as well as western blotting to demonstrate the expression of proteins related to mitochondria functions. The expression of hypoxia-inducible factor-1 alpha (HIF-1 alpha) was diminished utilizing siRNA transfection. Results: Brain samples from KRGE-administered mice harbored an increased number of GFAP-expressing astrocytes. KRGE triggered the proliferation of astrocytes in vitro. Enhanced mitochondrial biogenesis induced by KRGE was detected using Mitotracker staining, ATP production, and O-2 consumption rate assays. The expression of proteins related to mitochondrial electron transport was increased in KRGE-treated astrocytes. These effects were blocked by HIF-1 alpha knockdown. The factors secreted from KRGE-treated astrocytes were determined, revealing the expression of various cytokines and growth factors, especially those related to angiogenesis and neurogenesis. KRGE-treated astrocyte conditioned media enhanced the differentiation of adult neural stem cells into mature neurons, increasing the migration of endothelial cells, and these effects were reduced in the background of HIF-1 alpha knockdown. Conclusion: Our findings suggest that KRGE exhibits prophylactic potential by stimulating astrocyte mitochondrial biogenesis through HIF-1 alpha, resulting in improved neurovascular function.
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