Relay-Version: version B 2.10 5/3/83; site utzoo.UUCP Posting-Version: version B 2.10.2 9/18/84; site gatech.CSNET Path: utzoo!watmath!clyde!burl!ulysses!gatech!carter From: carter@gatech.CSNET (Carter Bullard) Newsgroups: net.med Subject: Nutrasweet(psychological problems?) Message-ID: <617@gatech.CSNET> Date: Tue, 23-Jul-85 19:46:33 EDT Article-I.D.: gatech.617 Posted: Tue Jul 23 19:46:33 1985 Date-Received: Thu, 25-Jul-85 06:24:10 EDT Reply-To: carter@gatech.UUCP (Carter Bullard) Organization: School of ICS, Georgia Institute of Technology, Atlanta Lines: 41 Summary: Well, The effects of dietary phenylalanine in large quantities has been investigated to the point of absurdity since the early 60's, when phenylketonuria was being heavily researched. The documented behavioral changes in rodents and humans appear to be quite dramatic, in some cases causing symptoms similar to schizophrenia and/or general psychosis. This is of course not unexpected, since pheylalanine is the precursor for two neurotransmitters, norepinephrine and dopamine. Now dopamine is very interesting, since it has been successfully argued as a principle agent in the development of several types of psychosis. The greatest evidence that dopamine is involved in psychotic behavior is that most anti-psychotic drugs are very potent inhibitors of dopamine receptors. This has been demonstrated with both classical and molecular pharmacological techniques and is not disputed in the literature. In relation to aspartame, however, the problem is not simply that one of its metabolites is pheylalanine, rather it is that a portion of aspartame "looks" very similar to pheylalanine, and as a result could have a tendency to enter the dopamine pathway itself, if it can get into the brain without being metabolized. The odds of this happening are very good, since aspartame is rather cyclic and the pheylalanine "part" is rather exposed, making it available for active transport past the blood brain barrier and making the pheylalanine "part" available for interaction with dopamine related receptor sites. Remember that when aspartame was being first developed, it was described as a new amino acid derivative with unique properties. Aspartame in actuality is a brand new amino acid, not ever seen before in this universe. It is difficult to predict how the CNS will respond to a brand new amino acid that possesses unique properties as well as being physically similar to amino acids that the brain is currently using for its normal function. The problem that I have with all of this, then, is that the screening process for new compounds does not include tests for psychological effects, only tests for frank toxicity, teratogenic and carcinogenic problems. Any comments?