The effect of systemically applied cholinergic drugs on the striatal release of dopamine and its metabolites, as determined by automated brain dialysis in conscious rats

The effects of cholinergic drugs on the in vivo release of dopamine (DA) and its metabolites were studied in the striatum of freely moving rats. The endogenous compounds were sampled by microdialysis and analysed by on-line HPLC. High doses of oxotremorine (5 μmol/kg), physostigmine (3.6 μmol/kg), n...

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Veröffentlicht in:Neuroscience letters 1988-07, Vol.89 (3), p.349-354
Hauptverfasser: Damsma, Geert, Westerink, Ben H.C., de Vries, Jan B., Horn, Alan S.
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container_title Neuroscience letters
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creator Damsma, Geert
Westerink, Ben H.C.
de Vries, Jan B.
Horn, Alan S.
description The effects of cholinergic drugs on the in vivo release of dopamine (DA) and its metabolites were studied in the striatum of freely moving rats. The endogenous compounds were sampled by microdialysis and analysed by on-line HPLC. High doses of oxotremorine (5 μmol/kg), physostigmine (3.6 μmol/kg), nicotine (3 μmol/kg) and atropine (10 μmol/kg) were injected i.p. Oxotremorine, physostigmine and atropine failed to modify the release of DA, while nicotine induced a slight (30%) but significant increase in the release of the transmitter. In contrast, oxotremorine and physostigmine did produce a significant rise of the dialysate contents of the DA metabolites. Thus, these data demonstrate clearly that changes in DA metabolism do not necessarily reflect changes in the release of DA. The most interesting findings of the present study is the fact that muscarinic receptor stimulation or blockade does not modify the release of DA from the rat striatum, while nicotine receptor stimulation may exert some stimulatory effect on the release of DA. This conclusion does not support the concept that the mode of action of anticholinergic drugs used in the treatment of parkinsonism, can be ascribed to a modulation of striatal dopaminergic activity.
doi_str_mv 10.1016/0304-3940(88)90551-4
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The endogenous compounds were sampled by microdialysis and analysed by on-line HPLC. High doses of oxotremorine (5 μmol/kg), physostigmine (3.6 μmol/kg), nicotine (3 μmol/kg) and atropine (10 μmol/kg) were injected i.p. Oxotremorine, physostigmine and atropine failed to modify the release of DA, while nicotine induced a slight (30%) but significant increase in the release of the transmitter. In contrast, oxotremorine and physostigmine did produce a significant rise of the dialysate contents of the DA metabolites. Thus, these data demonstrate clearly that changes in DA metabolism do not necessarily reflect changes in the release of DA. The most interesting findings of the present study is the fact that muscarinic receptor stimulation or blockade does not modify the release of DA from the rat striatum, while nicotine receptor stimulation may exert some stimulatory effect on the release of DA. 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subjects 3,4-Dihydroxyphenylacetic Acid - metabolism
Animals
Atropine
Computers
Consciousness
Corpus Striatum - metabolism
Dialysis - methods
Dopamine
Dopamine - metabolism
Homovanillic Acid - metabolism
Hydroxyindoleacetic Acid - metabolism
Male
Microdialysis
Nicotine
Osmolar Concentration
Parasympathomimetics - pharmacology
Physostigmine
Rats
Rats, Inbred Strains
title The effect of systemically applied cholinergic drugs on the striatal release of dopamine and its metabolites, as determined by automated brain dialysis in conscious rats
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