C6H6
Bluelighter
- Joined
- Jan 29, 2005
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- 607
The effects of MDMA are thought to be caused mainly by its ability to reverse the function of the dopamine and 5-HT reuptake transporter and thus cause a massive release of dopamine and 5-HT. DMPP, chemically totally unrelated to MDMA, seems to have similar properties:
Neuropharmacology. 2005 Jun 29; [Epub ahead of print]
Carrier-mediated release of monoamines induced by the nicotinic acetylcholine receptor agonist DMPP.
Szasz BK, Mayer A, Zsilla G, Lendvai B, Vizi ES, Kiss JP.
Department of Pharmacology, Institute of Experimental Medicine, Hungarian Academy of Sciences, P.O.B. 67, H-1450 Budapest, Hungary.
We have previously shown that dimethylphenylpiperazinium (DMPP) increases the release of noradrenaline (NA) from rat hippocampal slices via two distinct mechanisms: a nicotinic acetylcholine receptor (nAChR)-mediated exocytosis and a carrier-mediated release induced by the reversal of NA transporters. Our aim was to investigate whether other monoaminergic systems are also affected by the multiple actions of DMPP. In our experiments DMPP dose-dependently increased the release of dopamine (DA) and serotonin (5-HT) from rat striatal and hippocampal slices, respectively. The dual effect was observed, however, only in case of DA at a lower DMPP concentration (30 muM), where the response was partly inhibited by mecamylamine, TTX and Ca(2+)-free medium (nAChR-mediated exocytosis) while the other part of the response was blocked only by the DA uptake inhibitor nomifensine (carrier-mediated release). In contrast, the DMPP-evoked 5-HT release and the DA release induced by high concentration DMPP was not inhibited by nicotinic antagonists, TTX and Ca(2+)-free medium but only by selective uptake inhibitors. In addition, DMPP dose-dependently inhibited the [(3)H]DA and [(3)H]5-HT uptake in striatal and hippocampal synaptosome preparation with an IC(50) of 3.18 and 0.49 muM, respectively. Our data show that DMPP interacts with monoamine transporters and induces a substantial carrier-mediated release of DA and 5-HT, therefore caution is needed for the interpretation of data, when this drug is used as a nAChR agonist.
PMID: 15993437