論文

査読有り 国際誌
2016年4月

Effects and mechanisms of prolongevity induced by Lactobacillus gasseri SBT2055 in Caenorhabditis elegans.

Aging cell
  • Hisako Nakagawa
  • ,
  • Takuya Shiozaki
  • ,
  • Eiji Kobatake
  • ,
  • Tomohiro Hosoya
  • ,
  • Tomohiro Moriya
  • ,
  • Fumihiko Sakai
  • ,
  • Hidenori Taru
  • ,
  • Tadaaki Miyazaki

15
2
開始ページ
227
終了ページ
36
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/acel.12431
出版者・発行元
WILEY-BLACKWELL

© 2016 The Anatomical Society and John Wiley & Sons Ltd. Lactic-acid bacteria are widely recognized beneficial host associated groups of the microbiota of humans and animals. Some lactic-acid bacteria have the ability to extend the lifespan of the model animals. The mechanisms behind the probiotic effects of bacteria are not entirely understood. Recently, we reported the benefit effects of Lactobacillus gasseriSBT2055 (LG2055) on animal and human health, such as preventing influenza A virus, and augmentation of IgA production. Therefore, it was preconceived that LG2055 has the beneficial effects on longevity and/or aging. We examined the effects of LG2055 on lifespan and aging of Caenorhabditis elegans and analyzed the mechanism of prolongevity. Our results demonstrated that LG2055 has the beneficial effects on longevity and anti-aging of C. elegans. Feeding with LG2055 upregulated the expression of the skn-1 gene and the target genes of SKN-1, encoding the antioxidant proteins enhancing antioxidant defense responses. We found that feeding with LG2055 directly activated SKN-1 activity via p38 MAPK pathway signaling. The oxidative stress response is elicited by mitochondrial dysfunction in aging, and we examined the influence of LG2055 feeding on the membrane potential of mitochondria. Here, the amounts of mitochondria were significantly increased by LG2055 feeding in comparison with the control. Our result suggests that feeding with LG2055 is effective to the extend lifespan in C. elegans by a strengthening of the resistance to oxidative stress and by stimulating the innate immune response signaling including p38MAPK signaling pathway and others.

リンク情報
DOI
https://doi.org/10.1111/acel.12431
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/26710940
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783334
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000372880500004&DestApp=WOS_CPL
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84960077952&origin=inward 本文へのリンクあり
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=84960077952&origin=inward
ID情報
  • DOI : 10.1111/acel.12431
  • ISSN : 1474-9718
  • eISSN : 1474-9726
  • PubMed ID : 26710940
  • PubMed Central 記事ID : PMC4783334
  • SCOPUS ID : 84960077952
  • Web of Science ID : WOS:000372880500004

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