Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats - PubMed (original) (raw)
Comparative Study
Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats
G Di Chiara et al. Proc Natl Acad Sci U S A. 1988 Jul.
Abstract
The effect of various drugs on the extracellular concentration of dopamine in two terminal dopaminergic areas, the nucleus accumbens septi (a limbic area) and the dorsal caudate nucleus (a subcortical motor area), was studied in freely moving rats by using brain dialysis. Drugs abused by humans (e.g., opiates, ethanol, nicotine, amphetamine, and cocaine) increased extracellular dopamine concentrations in both areas, but especially in the accumbens, and elicited hypermotility at low doses. On the other hand, drugs with aversive properties (e.g., agonists of kappa opioid receptors, U-50,488, tifluadom, and bremazocine) reduced dopamine release in the accumbens and in the caudate and elicited hypomotility. Haloperidol, a neuroleptic drug, increased extracellular dopamine concentrations, but this effect was not preferential for the accumbens and was associated with hypomotility and sedation. Drugs not abused by humans [e.g., imipramine (an antidepressant), atropine (an antimuscarinic drug), and diphenhydramine (an antihistamine)] failed to modify synaptic dopamine concentrations. These results provide biochemical evidence for the hypothesis that stimulation of dopamine transmission in the limbic system might be a fundamental property of drugs that are abused.
Similar articles
- Does amphetamine preferentially increase the extracellular concentration of dopamine in the mesolimbic system of freely moving rats?
Robinson TE, Camp DM. Robinson TE, et al. Neuropsychopharmacology. 1990 Jun;3(3):163-73. Neuropsychopharmacology. 1990. PMID: 1694669 - Preferential stimulation of dopamine release in the nucleus accumbens of freely moving rats by ethanol.
Imperato A, Di Chiara G. Imperato A, et al. J Pharmacol Exp Ther. 1986 Oct;239(1):219-28. J Pharmacol Exp Ther. 1986. PMID: 3761194 - Mechanisms underlying δ- and μ-opioid receptor agonist-induced increases in extracellular dopamine level in the nucleus accumbens of freely moving rats.
Saigusa T, Aono Y, Waddington JL. Saigusa T, et al. J Oral Sci. 2017;59(2):195-200. doi: 10.2334/josnusd.16-0874. J Oral Sci. 2017. PMID: 28637978 Review. - Functional correlates of nicotine administration: similarity with drugs of abuse.
Pontieri FE, Passarelli F, Calò L, Caronti B. Pontieri FE, et al. J Mol Med (Berl). 1998 Mar;76(3-4):193-201. doi: 10.1007/s001090050208. J Mol Med (Berl). 1998. PMID: 9535552 Review.
Cited by
- Role of Dopamine Type 1 Receptors and Dopamine- and cAMP-Regulated Phosphoprotein Mr 32 kDa in Δ9-Tetrahydrocannabinol-Mediated Induction of ΔFosB in the Mouse Forebrain.
Lazenka MF, Tomarchio AJ, Lichtman AH, Greengard P, Flajolet M, Selley DE, Sim-Selley LJ. Lazenka MF, et al. J Pharmacol Exp Ther. 2015 Sep;354(3):316-27. doi: 10.1124/jpet.115.224428. Epub 2015 Jun 22. J Pharmacol Exp Ther. 2015. PMID: 26099530 Free PMC article. - Housing conditions during self-administration determine motivation for cocaine in mice following chronic social defeat stress.
Engeln M, Fox ME, Lobo MK. Engeln M, et al. Psychopharmacology (Berl). 2021 Jan;238(1):41-54. doi: 10.1007/s00213-020-05657-y. Epub 2020 Sep 10. Psychopharmacology (Berl). 2021. PMID: 32914243 Free PMC article. - Targeting cAMP in D1-MSNs in the nucleus accumbens, a new rapid antidepressant strategy.
Zhang Y, Gao J, Li N, Xu P, Qu S, Cheng J, Wang M, Li X, Song Y, Xiao F, Yang X, Liu J, Hong H, Mu R, Li X, Wang Y, Xu H, Xie Y, Gao T, Wang G, Aa J. Zhang Y, et al. Acta Pharm Sin B. 2024 Feb;14(2):667-681. doi: 10.1016/j.apsb.2023.12.005. Epub 2023 Dec 19. Acta Pharm Sin B. 2024. PMID: 38322327 Free PMC article. - Current and emerging pharmacotherapies for opioid dependence treatments in adults: a comprehensive update.
Leyrer-Jackson JM, Acuña AM, Olive MF. Leyrer-Jackson JM, et al. Expert Opin Pharmacother. 2022 Nov;23(16):1819-1830. doi: 10.1080/14656566.2022.2140039. Epub 2022 Nov 14. Expert Opin Pharmacother. 2022. PMID: 36278879 Free PMC article. Review. - Reversal of quinpirole inhibition of ventral tegmental area neurons is linked to the phosphatidylinositol system and is induced by agonists linked to G(q).
Nimitvilai S, McElvain MA, Arora DS, Brodie MS. Nimitvilai S, et al. J Neurophysiol. 2012 Jul;108(1):263-74. doi: 10.1152/jn.01137.2011. Epub 2012 Apr 4. J Neurophysiol. 2012. PMID: 22490559 Free PMC article.
References
- Brain Res. 1982 Dec 16;253(1-2):185-93 - PubMed
- J Pharmacol Exp Ther. 1983 Jan;224(1):7-12 - PubMed
- J Neurochem. 1983 Dec;41(6):1769-73 - PubMed
- Brain Res. 1984 Jan 30;292(1):63-9 - PubMed
- J Neurosci. 1984 Apr;4(4):966-77 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources