Energetics and mammary carcinogenesis: effects of moderate-intensity running and energy intake on cellular processes and molecular mechanisms in rats

Cancer Prevention Laboratory, Colorado State University, Fort Collins, Colorado Submitted 8 September 2008 ; accepted in final form 15 December 2008 The objective of this experiment was to determine the effects on mammary carcinogenesis of similar limitations in energy availability either by energy...

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Published in:Journal of applied physiology (1985) Vol. 106; no. 3; pp. 911 - 918
Main Authors: Zhu, Zongjian, Jiang, Weiqin, McGinley, John N, Thompson, Henry J
Format: Journal Article
Language:English
Published: Bethesda, MD Am Physiological Soc 01-03-2009
American Physiological Society
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Summary:Cancer Prevention Laboratory, Colorado State University, Fort Collins, Colorado Submitted 8 September 2008 ; accepted in final form 15 December 2008 The objective of this experiment was to determine the effects on mammary carcinogenesis of similar limitations in energy availability either by energy expenditure due to moderate-intensity running (physical activity, PA) or by regulating dietary energy (RE) intake relative to a sedentary control (SC) group that ate ad libitum. A total of 90 female Sprague-Dawley rats were injected with 1-methyl-1-nitrosourea (50 mg/kg) and 7 days thereafter were randomized to either SC, a PA group given free access to a motorized running wheel, or a RE group whose food intake limited growth to the rate observed in PA. Compared with SC, mammary carcinogenesis was inhibited by RE or PA. Cancer incidence, 92.6%, 77.8%, and 66.7% ( P = 0.06), and cancer multiplicity, 3.44, 2.11, and 1.62 cancers/rat ( P = 0.006), in SC, RE, and PA, respectively, were reduced to a similar extent by RE and PA. Histological and Western blot analyses of mammary carcinomas provided evidence that RE and PA induced apoptosis via the mitochondrial pathway, that cell cycle progression was suppressed at the G 1 /S transition, and that intratumoral blood vessel density was reduced, although it remains to be determined whether PA and RE exert these effects via the same mechanisms. energy restriction; physical activity Address for reprint requests and other correspondence: H. J. Thompson, Cancer Prevention Laboratory, Colorado State Univ., 1173 Campus Delivery, Fort Collins, CO 80523 (e-mail: henry.thompson{at}colostate.edu )
Bibliography:The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
ISSN:8750-7587
1522-1601
DOI:10.1152/japplphysiol.91201.2008