THE EFFECT OF EARLY CALORIC RESTRICTION ON COLONIC CELLULAR GROWTH IN RATS

被引:24
作者
ALBANES, D
SALBE, AD
LEVANDER, OA
TAYLOR, PR
NIXON, DW
WINICK, M
机构
[1] Cancer Prevention Research Program, Division of Cancer Prevention and Control, National Cancer Institute, National Institutes of Health, Bethesda
[2] US Department of Agriculture, Human Nutrition Research Center, Beltsville
来源
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL | 1990年 / 13卷 / 1-2期
基金
美国国家卫生研究院;
关键词
D O I
10.1080/01635589009514047
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although the inhibitory effect of caloric restriction on tumorigenesis is substantial and well known, the pertinent mechanisms remain to be determined. We recently suggested that the risk of cancer may be directly related to the total number of dividing cells within an affected organ. This study evaluates the effects of early caloric restriction on the cellular growth of the colon. The experiment began one day postpartum and ended six weeks later with the killing of all animals. It consisted of two consecutive periods: a) three weeks of suckling and b) three weeks postweaning. Animals whose food was restricted only during the suckling period showed normal colons when killed at six weeks. Caloric restriction (40%) for three weeks postweaning resulted in colons of lower weight with fewer cells (less total DNA) and reduced total DNA synthesis ([3H]thymidine uptake, dpm/colon) when compared with animals fed ad libitum postweaning. Conversely, only rats fed ad libitum from birth through the first three weeks after weaning demonstrated an increase (21%) in the rate of DNA synthesis (dpm/mg DNA) compared with other animals, In addition, the colonic crypts showed no differences in the number of cells or the number of dividing cells, as determined by autoradiography. By contrast, the total number of crypts (and/or the number of mucosal cells between crypts) are reduced, and hence the total number of colonic mucosal cells dividing at any given time are similarly decreased. The reduced number of dividing cells in the colons of these animals (i.e., those restricted postweaning) could explain previous data suggesting that they are resistant to the induction of colon cancer. © 1990, Taylor & Francis Group, LLC. All rights reserved.
引用
收藏
页码:73 / 80
页数:8
相关论文
共 20 条
  • [1] Winick M., Noble A., Quantitative Changes in DNA, RNA and Protein During Prenatal and Postnatal Growth in the Rat, Dev Biol, 12, pp. 451-465, (1965)
  • [2] Winick M., Noble A., Cellular Response in Rats During Malnutrition at Various Ages, J Nutr, 89, pp. 300-306, (1966)
  • [3] Winick M., Noble A., Cellular Response With Increased Feeding in Neonatal Rats, J Nutr, 91, pp. 179-187, (1967)
  • [4] Albanes D., Winick M., Are Cell Number and Cell Proliferation Risk Factors for Cancer, JNCI, 80, pp. 772-775, (1988)
  • [5] Ross M.H., Bras G., Lasting Influe ice of Early Caloric Restriction on Prevalence of Neoplasms in the Rat, JNCI, 47, pp. 1095-1113, (1971)
  • [6] Albanes D., Jones D.Y., Schatzkin A., Micozzi M.S., Taylor P.R., Adult Stature and Risk of Cancer, Cancer Res, 48, pp. 1658-1662, (1988)
  • [7] Swanson C.A., Jones D.Y., Schatzkin A., Brinton L.A., Ziegler R.G., Breast Cancer Risk Assessed by Anthropometry in the NHANES I Epidemiological Follow-Up Study, Cancer Res, 48, pp. 5363-5367, (1988)
  • [8] Hirsch J., Ahrens E.H., Blankenhorn D.H., Measurement of the Human Intestinal Length in vivo and Some Causes of Variation, Gastroenterology, 31, pp. 274-284, (1956)
  • [9] Ruggeri B.A., Klurfeld D.M., Kritchevsky D., Biochemical Alterations in 7,12-Dimethylbenz[α]anthracene-induced Mammary Tumors From Rats Subjected to Caloric Restriction, Biochim Biophys Acta, 929, pp. 239-246, (1987)
  • [10] Munro H.N., Fleck A., Recent Developments in the Measurement of Nucleic Acids in Biological Materials, Analyst, 91, pp. 78-88, (1966)