REDUCTION IN RATE OF OCCURRENCE OF AGE-RELATED LESIONS IN DIETARY RESTRICTED LABORATORY MICE

被引:0
|
作者
BRONSON, RT
LIPMAN, RD
机构
[1] TUFTS UNIV, SCH VET MED, DEPT PATHOL, BOSTON, MA 02111 USA
[2] TUFTS UNIV, SCH MED, DEPT PATHOL, BOSTON, MA 02111 USA
来源
GROWTH DEVELOPMENT AND AGING | 1991年 / 55卷 / 03期
关键词
AGING; FOOD RESTRICTION; BIOMARKERS OF AGING; MOUSE; PATHOLOGY; CANCER;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
This report describes the results of a study to find differences in the distribution of pathologic lesions between 40% dietary restricted (DR) and ad libitum (AL) fed mice of four genotypes, C57BL/6NNia, DBA/2NNia, B6D2F1NNia and B6C3FlNNia. Representative samples of all organs were studied from 1134 mice killed at 12, 18, 24 and 30 months of age. Approximately half were female, half male. All mice were fed a natural ingredient diet, NIH-31 and were maintained under pathogen free conditions. A total of 135 lesions was observed. The rate of occurrence of each of 35 common lesions is described for each age/genotype/sex in the study. Fifteen lesions are described in detail. Highly significant differences were found between mice of the same age, sex and genotype in the two diet groups in the percent rate of occurrence of total lesions, total tumors, and total lymphoid nodules of various organs. These parameters generally increased with age in both diet groups. For example, of female mice of all genotypes at 24 months, 51% AL and 13% DR mice had tumors. These percentages were 123% and 17% respectively at 30 months. The evidence presented here suggests that total tumors, total lymphoid nodules, total lesions, and absence of lesions are all useful measures of aging, independent of the life span, that reflect the long known effect of dietary restriction on reducing the rate of aging. These parameters, however, only partially reflected the longer life span of hybrid as compared with inbred mice.
引用
收藏
页码:169 / 184
页数:16
相关论文
共 50 条
  • [1] AGE-RELATED SPONTANEOUS UTERINE LESIONS IN MICE
    MALININ, GI
    MALININ, IM
    JOURNALS OF GERONTOLOGY, 1972, 27 (02): : 193 - &
  • [2] LONGEVITY AND AGE-RELATED LESIONS IN A LABORATORY COLONY OF GRASSHOPPER MICE, ONYCHOMYS-LEUCOGASTER
    OFARRELL, TP
    COSGROVE, GE
    AMERICAN MIDLAND NATURALIST, 1975, 94 (01): : 241 - 247
  • [3] Is there evidence for an age-related reduction in metabolic rate?
    Piers, LS
    Soares, MJ
    McCormack, LM
    O'Dea, K
    JOURNAL OF APPLIED PHYSIOLOGY, 1998, 85 (06) : 2196 - 2204
  • [4] Genetic loci contributing to age-related hippocampal lesions in mice
    Krass, KL
    Colinayo, V
    Ghazalpour, A
    Vinters, HV
    Lusis, AJ
    Drake, TA
    NEUROBIOLOGY OF DISEASE, 2003, 13 (02) : 102 - 108
  • [5] AGE-RELATED DIFFERENCES IN THE DISTRIBUTION AND OCCURRENCE OF ATHEROSCLEROTIC AORTIC LESIONS IN THE HYPERLIPEMIC RABBIT
    ORLANDI, A
    MAURIELLO, A
    DEANGELIS, C
    RAMACCI, MT
    SPAGNOLI, LG
    ARCHIVES OF GERONTOLOGY AND GERIATRICS, 1992, : 295 - 302
  • [6] Origins of Age-Related DNA Damage and Dietary Strategies for Its Reduction
    Gruz, Petr
    Shimizu, Masatomi
    REJUVENATION RESEARCH, 2010, 13 (2-3) : 285 - 287
  • [7] Accelerated onset of age-related autoimmune lesions in MRL/+ mice by ovariectomy
    Ishimaru, N
    Haneji, N
    Hamano, H
    Kumiko, Y
    Takahashi, M
    Hayashi, Y
    MECHANISMS OF AGEING AND DEVELOPMENT, 1997, 93 (1-3) : 145 - 156
  • [8] FAILURE OF DIETARY RESTRICTION TO RETARD AGE-RELATED NEUROCHEMICAL CHANGES IN MICE
    MAY, PC
    TELFORD, N
    SALO, D
    ANDERSON, C
    KOHAMA, SG
    FINCH, CE
    WALFORD, RL
    WEINDRUCH, R
    NEUROBIOLOGY OF AGING, 1992, 13 (06) : 787 - 791
  • [9] Dietary Lactoferrin Alleviates Age-Related Lacrimal Gland Dysfunction in Mice
    Kawashima, Motoko
    Kawakita, Tetsuya
    Inaba, Takaaki
    Okada, Naoko
    Ito, Masataka
    Shimmura, Shigeto
    Watanabe, Mitsuhiro
    Shinmura, Ken
    Tsubota, Kazuo
    PLOS ONE, 2012, 7 (03):
  • [10] Dietary fat and age-related maculopathy
    Friedman, E
    ARCHIVES OF OPHTHALMOLOGY, 1996, 114 (02) : 235 - 236