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Schizophrenia treatment (Edited former post)

Posted by Shawn. T. on July 15, 2002, at 20:20:53

Aventis Pharmaceuticals will likely soon be releasing a potent new drug for schizophrenia, M,100,907. M,100,907 is a potent 5-HT2 antagonist. It has the same, perhaps even better, effects as current drugs available for the treatment of schizophrenia, only without the extrapyramidal side effects (e.g. effects on motor control). Take for example Zyprexa (Olanzapine). Zyprexa exerts its effects on a very wide range of receptors. http://www.gpcr.org/7tm/ligand/Organon/Tablig/LIG_C132539061.html

Zyprexa's 5-HT1a receptor effects are within the range of weakly active, so that rules out 5-HT (serotonin) when explaining Zyprexa's efficacy. With regards to the dopamine receptors, the evidence seems to show that their activation is not necessary for the treatment of schizophrenia and leads to increased extrapyramidal side effects.
http://www4.infotrieve.com/search/databases/detailsNew.asp?artID=1986311

With regards to NAa1, I am unaware of any reasoning that would support a role for it in schizophrenia. The effects on acetylcholine are unnecessary and produce side effects. Effects on histamine receptors, however, are transient and should disappear after a few weeks. This would seem to imply 5-HT2 antagonism as the mechanism of schizophrenia efficacy in Zyprexa.

As mentioned in the study provided above, 5-HT2 antagonism is the key to treating schizophrenia. The extra effects on receptors unrelated to schizophrenia seen in current treatments are providing all of the negative effects of these drugs. M,100,907 would provide all of the positive effects of 5-HT2 antagonism and none of the negative effects caused by anticholinergic, antihistamine, and dopaminergic actions. I suggest that M,100,907, among other positive actions, helps to modulate dopamine release. It would serve to prevent spikes in dopamine release in response to stressors or the introduction of drugs such as amphetamines (these drugs cause something similary to psychosis in high doses). See
http://www4.infotrieve.com/search/databases/detailsNew.asp?artID=24612534
With regards to the negative and positive effects of schizophrenia and how M,100,907 affects these, see
http://www4.infotrieve.com/search/databases/detailsNew.asp?artID=7411933
and
http://www4.infotrieve.com/search/databases/detailsNew.asp?artID=11283291
Also examine the following study for an explanation of hallucinations in schizophrenic patients:
http://www4.infotrieve.com/search/databases/detailsNew.asp?artID=24922782

Moreover, a 5-HT2 antagonist, Mirtazapine (Remeron), has been given regulatory approval in the United States. For this reason, I would suggest that a 5-HT2 antagonist would be a very tolerable agent to cure schizophrenia. M,100,907 has been shown to be more effective than both clozapine and haloperidol. Until M,100,907 is released, I would suggest that Remeron is currently the drug with the fewest side effects for the treatment of schizophrenia.
http://www.biopsychiatry.com/mirtaznegschizo.htm

The drug company Aventis has the rights to M,100,907.
http://www.aventis.com/main/0,1003,EN-XX-24620-36860--,FF.html


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poster:Shawn. T. thread:112472
URL: http://www.dr-bob.org/babble/20020709/msgs/112472.html