Red Ginseng Attenuates the Hepatic Cellular Senescence in Aged Mice

Cellular senescence is defined as an irreversible cell cycle arrest accompanied by morphological and physiological alterations during aging. Red ginseng (RG), processed from fresh ginseng (<i>Panax ginseng</i> C.A. Meyer) with a one-time steaming and drying process, is a well-known benef...

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Main Authors: Da-Yeon Lee, Juliana Arndt, Jennifer F. O’Connell, Josephine M. Egan, Yoo Kim
Format: Article
Language:English
Published: MDPI AG 2024-01-01
Series:Biology
Subjects:
Online Access:https://www.mdpi.com/2079-7737/13/1/36
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author Da-Yeon Lee
Juliana Arndt
Jennifer F. O’Connell
Josephine M. Egan
Yoo Kim
author_facet Da-Yeon Lee
Juliana Arndt
Jennifer F. O’Connell
Josephine M. Egan
Yoo Kim
author_sort Da-Yeon Lee
collection DOAJ
description Cellular senescence is defined as an irreversible cell cycle arrest accompanied by morphological and physiological alterations during aging. Red ginseng (RG), processed from fresh ginseng (<i>Panax ginseng</i> C.A. Meyer) with a one-time steaming and drying process, is a well-known beneficial herbal medicine showing antioxidant, anti-inflammatory, and anti-aging properties. The current study aimed to investigate the benefits of RG in alleviating hepatic cellular senescence and its adverse effects in 19-month-old aged mice. We applied two different intervention methods and durations to compare RG’s effects in a time-dependent manner: (1) oral gavage injection for 4 weeks and (2) ad libitum intervention for 14 weeks. We observed that 4-week RG administration was exerted to maintain insulin homeostasis against developing age-associated insulin insensitivity and suppressed cellular senescence pathway in the liver and primary hepatocytes. Moreover, with remarkable improvement of insulin homeostasis, 14-week RG supplementation downregulated the activation of c-Jun N-terminal kinase (JNK) and its downstream transcriptional factor nuclear factor-κB (NF-κB) in aged mice. Lastly, RG treatment significantly reduced the senescence-associated β-galactosidase (SA-β-gal)-positive cells in primary hepatocytes and ionizing radiation (IR)-exposed mouse embryonic fibroblasts (MEFs). Taken together, we suggest that RG can be a promising candidate for a senolytic substance by preventing hepatic cellular senescence.
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spelling doaj.art-d6fb219b40ee41978519e844b6b1404a2024-01-26T15:06:57ZengMDPI AGBiology2079-77372024-01-011313610.3390/biology13010036Red Ginseng Attenuates the Hepatic Cellular Senescence in Aged MiceDa-Yeon Lee0Juliana Arndt1Jennifer F. O’Connell2Josephine M. Egan3Yoo Kim4Department of Nutritional Sciences, Oklahoma State University, Stillwater, OK 74078, USADepartment of Nutritional Sciences, Oklahoma State University, Stillwater, OK 74078, USALaboratory of Clinical Investigation, National Institute on Aging, Baltimore, MD 21224, USALaboratory of Clinical Investigation, National Institute on Aging, Baltimore, MD 21224, USADepartment of Nutritional Sciences, Oklahoma State University, Stillwater, OK 74078, USACellular senescence is defined as an irreversible cell cycle arrest accompanied by morphological and physiological alterations during aging. Red ginseng (RG), processed from fresh ginseng (<i>Panax ginseng</i> C.A. Meyer) with a one-time steaming and drying process, is a well-known beneficial herbal medicine showing antioxidant, anti-inflammatory, and anti-aging properties. The current study aimed to investigate the benefits of RG in alleviating hepatic cellular senescence and its adverse effects in 19-month-old aged mice. We applied two different intervention methods and durations to compare RG’s effects in a time-dependent manner: (1) oral gavage injection for 4 weeks and (2) ad libitum intervention for 14 weeks. We observed that 4-week RG administration was exerted to maintain insulin homeostasis against developing age-associated insulin insensitivity and suppressed cellular senescence pathway in the liver and primary hepatocytes. Moreover, with remarkable improvement of insulin homeostasis, 14-week RG supplementation downregulated the activation of c-Jun N-terminal kinase (JNK) and its downstream transcriptional factor nuclear factor-κB (NF-κB) in aged mice. Lastly, RG treatment significantly reduced the senescence-associated β-galactosidase (SA-β-gal)-positive cells in primary hepatocytes and ionizing radiation (IR)-exposed mouse embryonic fibroblasts (MEFs). Taken together, we suggest that RG can be a promising candidate for a senolytic substance by preventing hepatic cellular senescence.https://www.mdpi.com/2079-7737/13/1/36red ginsenglivercellular senescenceinflammationapoptosisinsulin homeostasis
spellingShingle Da-Yeon Lee
Juliana Arndt
Jennifer F. O’Connell
Josephine M. Egan
Yoo Kim
Red Ginseng Attenuates the Hepatic Cellular Senescence in Aged Mice
Biology
red ginseng
liver
cellular senescence
inflammation
apoptosis
insulin homeostasis
title Red Ginseng Attenuates the Hepatic Cellular Senescence in Aged Mice
title_full Red Ginseng Attenuates the Hepatic Cellular Senescence in Aged Mice
title_fullStr Red Ginseng Attenuates the Hepatic Cellular Senescence in Aged Mice
title_full_unstemmed Red Ginseng Attenuates the Hepatic Cellular Senescence in Aged Mice
title_short Red Ginseng Attenuates the Hepatic Cellular Senescence in Aged Mice
title_sort red ginseng attenuates the hepatic cellular senescence in aged mice
topic red ginseng
liver
cellular senescence
inflammation
apoptosis
insulin homeostasis
url https://www.mdpi.com/2079-7737/13/1/36
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AT julianaarndt redginsengattenuatesthehepaticcellularsenescenceinagedmice
AT jenniferfoconnell redginsengattenuatesthehepaticcellularsenescenceinagedmice
AT josephinemegan redginsengattenuatesthehepaticcellularsenescenceinagedmice
AT yookim redginsengattenuatesthehepaticcellularsenescenceinagedmice