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Extracts of Cistanche deserticola Can Antagonize Immunosenescence and Extend Life Span in Senescence-Accelerated Mouse Prone 8 (SAM-P8) Mice

The senescence accelerated mouse prone 8 substrain (SAM-P8), widely accepted as an animal model for studying aging and antiaging drugs, was used to examine the effects of dietary supplementation with extracts of Cistanche deserticola (ECD) which has been used extensively in traditional Chinese medic...

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Autores principales: Zhang, Ke, Ma, Xu, He, Wenjun, Li, Haixia, Han, Shuyan, Jiang, Yong, Wu, Hounan, Han, Li, Ohno, Tomohiro, Uotsu, Nobuo, Yamaguchi, Kohji, Ma, Zhizhong, Tu, Pengfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913196/
https://www.ncbi.nlm.nih.gov/pubmed/24523825
http://dx.doi.org/10.1155/2014/601383
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author Zhang, Ke
Ma, Xu
He, Wenjun
Li, Haixia
Han, Shuyan
Jiang, Yong
Wu, Hounan
Han, Li
Ohno, Tomohiro
Uotsu, Nobuo
Yamaguchi, Kohji
Ma, Zhizhong
Tu, Pengfei
author_facet Zhang, Ke
Ma, Xu
He, Wenjun
Li, Haixia
Han, Shuyan
Jiang, Yong
Wu, Hounan
Han, Li
Ohno, Tomohiro
Uotsu, Nobuo
Yamaguchi, Kohji
Ma, Zhizhong
Tu, Pengfei
author_sort Zhang, Ke
collection PubMed
description The senescence accelerated mouse prone 8 substrain (SAM-P8), widely accepted as an animal model for studying aging and antiaging drugs, was used to examine the effects of dietary supplementation with extracts of Cistanche deserticola (ECD) which has been used extensively in traditional Chinese medicine because of its perceived ability to promote immune function in the elderly. Eight-month-old male SAM-P8 mice were treated with ECD by daily oral administrations for 4 weeks. The results showed that dietary supplementation of 150 mg/kg and 450 mg/kg of ECD could extend the life span measured by Kaplan-Meier survival analysis in dose-dependent manner. Dietary supplementation of SAM-P8 mice for 4 weeks with 100, 500, and 2500 mg/kg of ECD was shown to result in significant increases in both naive T and natural killer cells in blood and spleen cell populations. In contrast, peripheral memory T cells and proinflammatory cytokine, IL-6 in serum, were substantially decreased in the mice that ingested 100 and 500 mg/kg of ECD daily. Additionally, Sca-1 positive cells, the recognized progenitors of peripheral naive T cells, were restored in parallel. Our results provide clear experimental support for long standing clinical observational studies showing that Cistanche deserticola possesses significant effects in extending life span and suggest this is achieved by antagonizing immunosenescence.
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spelling pubmed-39131962014-02-12 Extracts of Cistanche deserticola Can Antagonize Immunosenescence and Extend Life Span in Senescence-Accelerated Mouse Prone 8 (SAM-P8) Mice Zhang, Ke Ma, Xu He, Wenjun Li, Haixia Han, Shuyan Jiang, Yong Wu, Hounan Han, Li Ohno, Tomohiro Uotsu, Nobuo Yamaguchi, Kohji Ma, Zhizhong Tu, Pengfei Evid Based Complement Alternat Med Research Article The senescence accelerated mouse prone 8 substrain (SAM-P8), widely accepted as an animal model for studying aging and antiaging drugs, was used to examine the effects of dietary supplementation with extracts of Cistanche deserticola (ECD) which has been used extensively in traditional Chinese medicine because of its perceived ability to promote immune function in the elderly. Eight-month-old male SAM-P8 mice were treated with ECD by daily oral administrations for 4 weeks. The results showed that dietary supplementation of 150 mg/kg and 450 mg/kg of ECD could extend the life span measured by Kaplan-Meier survival analysis in dose-dependent manner. Dietary supplementation of SAM-P8 mice for 4 weeks with 100, 500, and 2500 mg/kg of ECD was shown to result in significant increases in both naive T and natural killer cells in blood and spleen cell populations. In contrast, peripheral memory T cells and proinflammatory cytokine, IL-6 in serum, were substantially decreased in the mice that ingested 100 and 500 mg/kg of ECD daily. Additionally, Sca-1 positive cells, the recognized progenitors of peripheral naive T cells, were restored in parallel. Our results provide clear experimental support for long standing clinical observational studies showing that Cistanche deserticola possesses significant effects in extending life span and suggest this is achieved by antagonizing immunosenescence. Hindawi Publishing Corporation 2014 2014-01-09 /pmc/articles/PMC3913196/ /pubmed/24523825 http://dx.doi.org/10.1155/2014/601383 Text en Copyright © 2014 Ke Zhang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Ke
Ma, Xu
He, Wenjun
Li, Haixia
Han, Shuyan
Jiang, Yong
Wu, Hounan
Han, Li
Ohno, Tomohiro
Uotsu, Nobuo
Yamaguchi, Kohji
Ma, Zhizhong
Tu, Pengfei
Extracts of Cistanche deserticola Can Antagonize Immunosenescence and Extend Life Span in Senescence-Accelerated Mouse Prone 8 (SAM-P8) Mice
title Extracts of Cistanche deserticola Can Antagonize Immunosenescence and Extend Life Span in Senescence-Accelerated Mouse Prone 8 (SAM-P8) Mice
title_full Extracts of Cistanche deserticola Can Antagonize Immunosenescence and Extend Life Span in Senescence-Accelerated Mouse Prone 8 (SAM-P8) Mice
title_fullStr Extracts of Cistanche deserticola Can Antagonize Immunosenescence and Extend Life Span in Senescence-Accelerated Mouse Prone 8 (SAM-P8) Mice
title_full_unstemmed Extracts of Cistanche deserticola Can Antagonize Immunosenescence and Extend Life Span in Senescence-Accelerated Mouse Prone 8 (SAM-P8) Mice
title_short Extracts of Cistanche deserticola Can Antagonize Immunosenescence and Extend Life Span in Senescence-Accelerated Mouse Prone 8 (SAM-P8) Mice
title_sort extracts of cistanche deserticola can antagonize immunosenescence and extend life span in senescence-accelerated mouse prone 8 (sam-p8) mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913196/
https://www.ncbi.nlm.nih.gov/pubmed/24523825
http://dx.doi.org/10.1155/2014/601383
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