Tetrahydropapaveroline injected in the ventral tegmental area shifts dopamine efflux differentially in the shell and core of nucleus accumbens in high-ethanol-preferring (HEP) rats

被引:21
作者
Myers, RD [1 ]
Robinson, DE
机构
[1] E Carolina Univ, Sch Med, Dept Pharmacol, Greenville, NC 27858 USA
[2] E Carolina Univ, Sch Med, Ctr Alcohol & Drug Abuse Studies, Greenville, NC 27858 USA
关键词
tetrahydropapaveroline (THP); alcohol; opioid receptors; push-pull perfusion; alcoholism; dopamine amine metabolites; ventral tegmental area; nucleus accumbens;
D O I
10.1016/S0741-8329(99)00008-7
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Since the 1970s tetrahydropapaveroline (THP) and other tetrahydroisoquinoline alkaloids have been implicated in the etiology of alcoholism. When injected into the cerebral ventricle or at specific sites in the mesolimbic system such as the ventral tegmental area (VTA), THP evokes spontaneous and intense intake of alcohol in the nondrinking animal. Further, THP evokes the extracellular efflux of dopamine in the nucleus accumbens (NAC), which comprises, in part, the postulated alcohol drinking "circuit" of neurons. The purpose of this study was to characterize the action of a THP reactive structure, the VTA, on the activity of dopamine and its metabolism in the NAC. In the anesthetized high-ethanol preferring (HEP) rat, artificial CSF was perfused for 10 min at a rate of 10 mu l per min specifically in either the core or shell of the NAC. A microbore push-pull cannula system was selected over a microdialysis probe because of its superior recovery of neurotransmitters and tip exposure of less than 1.0 mm. After a series of 5-min perfusions, a single microinjection of 5.0 mu g/mu l of THP was made in the ipsilateral VTA while the NAC was perfused simultaneously. Sequential samples of the NAC perfusate were assayed by an HPLC coulometric system to quantitate the concentrations of dopamine and its metabolites, DOPAC and HVA, as well as the 5-HT metabolite, 5-HIAA. The results showed that THP injected in the VTA caused a significant increase by 94 +/- 23% in the efflux of dopamine from the core of the NAC. Conversely, the THP injected identically in the VTA suppressed the efflux of dopamine within the shell of the NAC by 51 +/- 10%. The levels of DOPAC, HVA and 5-HIAA within the core and shell of the NAC generally paralleled the increase and decrease in efflux, respectively, of dopamine. CSF control injections in the VTA as well as injections outside of the VTA failed to alter dopamine or metabolite activity in the NAC. These results demonstrate that the presence of THP in the VTA alters directly the function of the pathway of mesolimbic neurons generally and the dopaminergic system specifically. That such a perturbation could account for the induction of alcohol preference is proposed in relation to a reinforcing mechanism involving opioidergic and dopaminergic elements. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:83 / 90
页数:8
相关论文
共 31 条
  • [11] Ethanol drinking reduces extracellular dopamine levels in the posterior ventral tegmental area of nondependent alcohol-preferring rats
    Engleman, Eric A.
    Keen, Elizabeth J.
    Tilford, Sydney S.
    Thielen, Richard J.
    Morzorati, Sandra L.
    [J]. ALCOHOL, 2011, 45 (06) : 549 - 557
  • [12] Characterization of orexin input to dopamine neurons of the ventral tegmental area projecting to the medial prefrontal cortex and shell of nucleus accumbens
    Kallo, Imre
    Omrani, Azar
    Meye, Frank J.
    de Jong, Han
    Liposits, Zsolt
    Adan, Roger A. H.
    [J]. BRAIN STRUCTURE & FUNCTION, 2022, 227 (03) : 1083 - 1098
  • [13] Ventral tegmental area α6β2 nicotinic acetylcholine receptors modulate phasic dopamine release in the nucleus accumbens core
    Wickham, Robert
    Solecki, Wojciech
    Rathbun, Liza
    McIntosh, J. Michael
    Addy, Nii A.
    [J]. PSYCHOPHARMACOLOGY, 2013, 229 (01) : 73 - 82
  • [14] Ventral tegmental area α6β2 nicotinic acetylcholine receptors modulate phasic dopamine release in the nucleus accumbens core
    Robert Wickham
    Wojciech Solecki
    Liza Rathbun
    J. Michael McIntosh
    Nii A. Addy
    [J]. Psychopharmacology, 2013, 229 : 73 - 82
  • [15] The neurotensin receptor antagonist SR 142948A blocks the efflux of dopamine evoked in nucleus accumbens by neurotensin ejection into the ventral tegmental area
    Leonetti, M
    Brun, P
    Sotty, F
    Steinberg, R
    Soubrié, P
    Bert, L
    Renaud, B
    Suaud-Chagny, MF
    [J]. NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2002, 365 (06) : 427 - 433
  • [16] Effect of cholecystokinin-8 microinjection into ventral tegmental area on dopamine release in nucleus accumbens of rats: An in vivo voltametric study
    Xie, JX
    Tang, M
    Zhang, CY
    [J]. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2001, 25 (02) : 427 - 434
  • [17] Nicotine differentially affects dopamine transmission in the nucleus accumbens shell and core of Lewis and Fischer 344 rats
    Cadoni, Cristina
    Muto, Tiziana
    Di Chiara, Gaetano
    [J]. NEUROPHARMACOLOGY, 2009, 57 (5-6) : 496 - 501
  • [18] Control of food intake by MC4-R signaling in the lateral hypothalamus, nucleus accumbens shell and ventral tegmental area: Interactions with ethanol
    Lerma-Cabrera, Jose M.
    Carvajal, Francisca
    de la Torre, Lourdes
    de la Fuente, Leticia
    Navarro, Montserrat
    Thiele, Todd E.
    Cubero, Inmaculada
    [J]. BEHAVIOURAL BRAIN RESEARCH, 2012, 234 (01) : 51 - 60
  • [19] Microinjection of neuropeptide S into the rat ventral tegmental area induces hyperactivity and increases extracellular levels of dopamine metabolites in the nucleus accumbens shell
    Mochizuki, Takahiro
    Kim, Juhyon
    Sasaki, Kazuo
    [J]. PEPTIDES, 2010, 31 (05) : 926 - 931
  • [20] Ethanol induces stronger dopamine release in nucleus accumbens (shell) of alcohol-preferring (bibulous) than in alcohol-avoiding (abstainer) rats
    Bustamante, Diego
    Elena Quintanilla, Maria
    Tampier, Lutske
    Gonzalez-Lira, Victor
    Israel, Yedy
    Herrera-Marschitz, Mario
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2008, 591 (1-3) : 153 - 158