THE EFFECTS OF OVERFEEDING AND DIETARY RESTRICTION ON SPRAGUE-DAWLEY RAT SURVIVAL AND EARLY PATHOLOGY BIOMARKERS OF AGING

被引:100
作者
KEENAN, KP
SMITH, PF
HERTZOG, P
SOPER, K
BALLAM, GC
CLARK, RL
机构
[1] Departments of Safety Assessment and Biometrics, Merck Research Laboratories, Purina Mills, West Point,St. Louis, Missouri
关键词
CALORIC RESTRICTION; CELL PROLIFERATION; BROMODEOXYURIDINE LABELING; PITUITARY HYPERPLASIA; NEOPLASIA; NEPHROPATHY; CARDIOMYOPATHY;
D O I
10.1177/019262339402200308
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A significant correlation exists between average daily food consumption and 2-yr survival in control ad libitum (AL)-fed Sprague-Dawley (SD) rats. SD rats were fed Purina Rodent Chow 5002 or a modified chow, 5002-9, with lower protein, fat, metabolizable energy and increased fiber AL or by dietary restriction (DR) to 65% of the AL amount by measurement or time (6.5 hr). At 52 wk, food consumption and key pathology biomarkers correlated with 106-wk survival. The modified chow, 5002-9 fed AL, did not significantly improve survival. SD rats fed either diet AL consumed the greatest amount of feed and kcal/rat but consumed the same amount of feed per gram body weight as DR-fed rats. At 52 wk, AL rats fed either diet had the same brain weights as DR rats, but the AL-fed rats had greater body weight and body fat content and increased heart, lung, kidney, liver, adrenal, thyroid, and pituitary weights as well as an increased incidence and severity of degenerative and/or proliferative lesions in these organs. This study demonstrates that overfeeding best correlates with low 2-yr survival in SD rats and that simple DR by caloric restriction modifies key pathology biomarkers in the pituitary, mammary gland, kidney, and heart of SD rats at 52 wk that are predictive of 106-wk survival.
引用
收藏
页码:300 / 315
页数:16
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共 74 条
[31]  
Maeda H., Gleiser C.A., Masoro E.J., Murata I., McMahan C.A., Yu B.P., Nutritional influences on aging of Fischer 344 rats 2, J. Gerontol, 40, pp. 671-688, (1985)
[32]  
Masoro E.J., CE F., EL S., Metabolism., Handbook of the Biology of Aging, pp. 540-563, (1985)
[33]  
Masoro E.J., Bianchi L., Holt P., OFW J., RN B., Extension of life span., Aging in Liver and Gastrointestinal Tract, pp. 49-58, (1988)
[34]  
Masoro E.J., Biology of aging: Facts, thoughts, and experimental approaches, Lab. Invest, 65, pp. 500-510, (1991)
[35]  
Masoro E.J., Use of rodents as models for the study of “normal aging”: Conceptual and practical issues, Neurobiol. Aging, 12, pp. 639-643, (1991)
[36]  
Masoro E.J., Aging and proliferative homeostasis: Modulation by food restriction in rodents, Lab. Animal Sci, 42, pp. 132-137, (1992)
[37]  
Masoro E.J., Iwasaki K., Gleiser C.A., McMahan C.A., Seo E.J., Yu B.P., Dietary modulation of the progression of nephropathy in aging rats: An evaluation of the importance of protein, Am. J. Clin. Nutr, 49, pp. 1217-1227, (1989)
[38]  
Masoro E.J., Katz M.S., McMahan C.A., Evidence for the glycation hypothesis of aging from the food-restricted rodent model, J. Gerontol, 44, pp. B20-B22, (1989)
[39]  
Masoro E.J., McCarter R.J.M., Aging as a consequence of fuel utilization, Aging, 3, pp. 117-128, (1991)
[40]  
Masoro E.J., McCarter R.J.M., Katz M.S., McMahan C.A., Dietary restriction alters characteristics of glucose fuel use, J. Gerontol, 47, pp. B202-B208, (1992)