Thursday, 6 November 2008

Glutamate and Schizophrenia.

I found this on one of the other sites here on Blogger (Medical News & Health).

"Is schizophrenia a disorder of glutamate hyperactivity or hypoactivity? While the predominant hypothesis for many years was that schizophrenia was a glutamate deficit disorder, there is growing evidence of glutamate hyperactivity as well. The study by Karlsson et al., appearing in the November 1st issue of Biological Psychiatry, reinforces this point with new data about the impact of deleting the gene for the glutamate transporter EAAT1. EAAT1, implicated in schizophrenia, plays a critical role in inactivating glutamate by removing it from the synaptic and extracellular spaces. The authors demonstrate that these “knockout” animals show increased responses to the NMDA glutamate receptor antagonist, MK-801. This drug causes the release of more glutamate into the synapse in the frontal cortex. This effect of MK-801 is reduced by a group II metabotropic glutamate receptor agonist, which reduces glutamate release. Dr. Andrew Holmes, corresponding author, further discusses their findings, “Our study adds a new twist to [glutamate] research by showing that genetically disrupting a major regulator of glutamate’s ability to communicate between nerve cells produces certain ’schizophrenia-like’ features in mice and, moreover, that these abnormalities can be corrected by a highly promising new class of glutamate-targeting antipsychotic treatments.” In fact, this class of drugs has already shown some preliminary efficacy in its ability to treat individuals suffering from schizophrenia.

John H. Krystal, M.D., Editor of Biological Psychiatry and affiliated with both Yale University School of Medicine and the VA Connecticut Healthcare System, comments: “The NMDA receptor antagonist model and the EAAT1 knockout animal push us to take a fresh look at the obstacles to treating cognitive impairments associated with schizophrenia, in other words, optimizing their cortical network function. This new look can lead us to drugs that would have been completely surprising as recently as 10 years ago, such as the group II metabotropic glutamate receptor agonists.”

Dr. Holmes does note that further research is warranted, stating, “What is now needed is more research to get a better handle on how disrupting this gene affects the brain’s neural wiring and molecular signaling pathways to produce the symptoms of schizophrenia.” This finding could ultimately help scientists develop new or improved treatments for this schizophrenia."


I find this article of great interest .... but what amazes me is that there is no mention of the involvement of glutamate in migraine, temporal lobe epilepsy and, of course, the Near-Death Experience.

It is possible that I am drawing conclusions when none should be (and, after all, I am not medically trained), but surely if glutamate is responsible for all these things where are the papers discussing why this may be? (a genuine question by the way)

1 comment:

Karl L Le Marcs said...

Tony: Hmmm, yes, rather interesting, not only for the content but also, as you say, for what is not discussed, ie. Glutamate in other conditions.

The article in question is "Loss of Glial Glutamate and Aspartate Transporter (Excitatory Amino Acid Transporter 1) Causes Locomotor Hyperactivity and Exaggerated Responses to Psychotomimetics: Rescue by Haloperidol and Metabotropic Glutamate 2/3 Agonist" (catchy title *smile*) by Rose-Marie Karlsson, Kohichi Tanaka, Markus Heilig, and Andrew Holmes.

Apparently the full article is available by contacting Elsevier, the publishers, and specifically a Jayne M.Dawkins (probably no relation but you never know) at ja.dawkins@elsevier.com, so it may be worth your while to contact them for a copy and to introduce CTF and ITLAD into the equation.

Link Below for more info:

Glutamte: Too Much Of A Good Thing In Schizophrenia?