HomeLarge Type Edition
HOME ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Services
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
PubMed
Right arrow PubMed Citation

Journals of Gerontology Series A: Biological Sciences and Medical Sciences, Vol 54, Issue 7 B276-B282, Copyright © 1999 by The Gerontological Society of America


JOURNAL ARTICLE

Aminoguanidine supplementation delays the onset of senescence in vitro in dermal fibroblast-like cells from senescence-accelerated mice

H Fujisawa, T Nishikawa, BH Zhu, Y Nishimura, M Shimizu, M Kimoto, K Higuchi and M Hosokawa
Field of Regeneration Control, Institute for Frontier Medical Sciences, Kyoto University, Japan.

The effects of aminoguanidine supplementation on senescence acceleration in vitro were examined in fibroblasts from the dorsal dermis of newborn SAMP11 (accelerated senescence-prone mice), and were compared to the effects in cell lines from SAMR1 (accelerated senescence-resistant) mice. Four millimolar aminoguanidine supplementation significantly delayed the senescence/crisis in cell lines from SAMP11 mice, but did not affect the senescence/crisis in cell lines from SAMR1 mice. Flow cytometric analysis of the DNA content of confluent cells revealed that aminoguanidine supplementation significantly decelerated the increase in the number of tetraploid cells until senescence/crisis. Although mean concentrations of lipid peroxides in the primary cultures did not differ significantly, considerably higher lipid peroxidation was observed in some SAMP11 cultures, and aminoguanidine supplementation reduced them to the levels in SAMRI cultures. These results strongly suggest that oxidative stress derived from polyamine catabolism may contribute to the senescence acceleration in vitro in cell lines from SAMP11 mice.


This article has been cited by other articles:


Home page
FASEB J.Home page
H. Atamna, A. Nguyen, C. Schultz, K. Boyle, J. Newberry, H. Kato, and B. N. Ames
Methylene blue delays cellular senescence and enhances key mitochondrial biochemical pathways
FASEB J, March 1, 2008; 22(3): 703 - 712.
[Abstract] [Full Text] [PDF]


Home page
Journals of Gerontology Series A: Biological Sciences and Medical SciencesHome page
Y. Chiba, Y. Yamashita, M. Ueno, H. Fujisawa, K. Hirayoshi, K.-i. Hohmura, H. Tomimoto, I. Akiguchi, M. Satoh, A. Shimada, et al.
Cultured Murine Dermal Fibroblast-Like Cells From Senescence-Accelerated Mice as In Vitro Models for Higher Oxidative Stress Due to Mitochondrial Alterations
J. Gerontol. A Biol. Sci. Med. Sci., September 1, 2005; 60(9): 1087 - 1098.
[Abstract] [Full Text] [PDF]




HOME ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by The Gerontological Society of America.