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a) a significant dose-related increase of malignant tumor-bearing animals in males, in particular in the group treated at 2000 ppm; b) a significant increase of the incidence in lymphomas/leukemias in males treated at 2000 ppm and a significant dose-related increase of the incidence of lymphomas/leukemias in females, in particular in the group treated at 2000 ppm; c) a significant dose-related increase of the incidence of mammary cancer in females, in particular in the group treated at 2000 ppm. Conclusions. The results of this carcinogenicity bioassay not only confirm, but also reinforce the first experimental demonstration of [aspartame's] multipotential carcinogenicity at a dose level close to the acceptable daily intake (ADI) for humans. Furthermore, the study demonstrates that when lifespan exposure to [aspartame] begins during fetal life, its carcinogenic effects are increased. The study, entitled "Lifespan Exposure to Low Doses of Aspartame Beginning During Prenatal Life Increases Cancer Effects in Rats" has been accepted for publication in the peer-reviewed journal Environmental Health Perspectives (EHP), the most widely-read environmental science journal in the world. This is the second study conducted by the Ramizzini Foundation documenting the cancer-causing effects of aspartame in animals. Most sane people, when faced with such evidence, would ask the obvious questions: Could aspartame also cause cancer in humans? Should we review the safety of aspartame just in case? Shutting down good science to protect profitsVirtually the entire health and medical system in the United States is not interested in these questions. Following the publication of this study, the U.S. Food and Drug Administration issued a statement flatly denying aspartame poses any safety risk whatsoever, rejecting the idea that its safety or approval as a food ingredient should be reviewed at all. Specifically, FDA spokesperson Michael Herndon said, "...the FDA finds no reason to alter its previous conclusion that aspartame is safe as a general purpose sweetener in food."In other words, the FDA is not interested in any new science that might challenge a decision it already made. Long live scientific-sounding dogma! As reported by the CSPI in a recent press release, According to a 1996 report in the Minneapolis Star Tribune, the FDA rejected repeated proposals by NIEHS to test aspartame using more modern methods than were originally used. David Rall, the former director of NIEHS and its National Toxicology Program, said, "any compound that is that widely used needs to be retested with modern methods every once in a while." The State of California, too, has urged new testing of aspartame. The FDA also rejected NIEHS's proposal to test acesulfame potassium, which CSPI says was "abysmally tested" by its manufacturer and showed signs of causing cancer in animals. Clearly, the FDA only hears what it wants to hear when it comes to protecting the highly profitable aspartame market. Those who have studied a bit of aspartame history know that aspartame was pushed through the FDA by none other than Donald Rumsfeld. Click here to read more articles on aspartame and its dubious history. Since the very beginning, the FDA has done everything in its power to protect the aspartame industry, including denying approval for the natural herbal sweetener stevia as a way to suppress the competition and protect the market for corporate-manufactured chemical sweeteners like aspartame. Get articles like this delivered to you FREE in our popular email newsletter Related CounterThink Cartoons:
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