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Aspartame administered in feed, beginning prenatally through life span, induces cancers of the liver and lung in male Swiss mice
Author(s) -
Soffritti Morando,
Belpoggi Fiorella,
Manservigi Marco,
Tibaldi Eva,
Lauriola Michelina,
Falcioni Laura,
Bua Luciano
Publication year - 2010
Publication title -
american journal of industrial medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.7
H-Index - 104
eISSN - 1097-0274
pISSN - 0271-3586
DOI - 10.1002/ajim.20896
Subject(s) - medicine , carcinogen , physiology , lung , incidence (geometry) , gestation , aspartame , life span , toxicity , pregnancy , endocrinology , biology , biochemistry , genetics , physics , optics , gerontology
Background Aspartame (APM) is a well‐known intense artificial sweetener used in more than 6,000 products. Among the major users of aspartame are children and women of childbearing age. In previous lifespan experiments conducted on Sprague–Dawley rats we have shown that APM is a carcinogenic agent in multiple sites and that its effects are increased when exposure starts from prenatal life. Objective The aim of this study is to evaluate the potential of APM to induce carcinogenic effects in mice. Methods Six groups of 62–122 male and female Swiss mice were treated with APM in feed at doses of 32,000, 16,000, 8,000, 2,000, or 0 ppm from prenatal life (12 days of gestation) until death. At death each animal underwent complete necropsy and all tissues and organs of all animals in the experiment were microscopically examined. Results APM in our experimental conditions induces in males a significant dose‐related increased incidence of hepatocellular carcinomas ( P < 0.01), and a significant increase at the dose levels of 32,000 ppm ( P < 0.01) and 16,000 ppm ( P < 0.05). Moreover, the results show a significant dose‐related increased incidence of alveolar/bronchiolar carcinomas in males ( P < 0.05), and a significant increase at 32,000 ppm ( P < 0.05). Conclusions The results of the present study confirm that APM is a carcinogenic agent in multiple sites in rodents, and that this effect is induced in two species, rats (males and females) and mice (males). No carcinogenic effects were observed in female mice. Am. J. Ind. Med. 53:1197–1206, 2010. © 2010 Wiley‐Liss, Inc.