Elsevier

Brain Research

Volume 94, Issue 3, 5 September 1975, Pages 507-522
Brain Research

Amphetamine and apomorphine responses in the rat following 6-OHDA lesions of the nucleus accumbens septi and corpus striatum

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Abstract

Eight μg of 6-hydroxydopamine (6-OHDA) injected bilaterally into the nucleus accumbens septi (NAS) or the caudate nucleus of the rat resulted in 79% and 50% depletion of endogenous dopamine (DA) at these respective sites. Fourteen days after the injection a low dose of amphetamine failed to induce the characteristic locomotor response in the NAS-lesioned rats but did so in the caudate-lesioned animals. By contrast the caudate lesion, but not the NAS lesion, abolished intense forms of stereotyped behaviour induced by higher doses of amphetamine. Both lesioned groups exhibited supersensitivity to the dopamine agonist, apomorphine; the NAS group showed enhanced locomotor activity and the caudate group enhanced stereotyped behaviour. The block of amphetamine locomotion and the enhanced response to apomorphine were maximal around 14 days after the operation and gradually attenuated up to 90 days. There is evidence that remaining DA levels in the NAS are greater at 90 than at 14 days postoperatively. Thus recovery of behavioural effects correlated with an increase in the remaining levels of DA in the NAS.

Reference (35)

  • Ande´nN.-E.

    Dopamine turnover in the corpus striatum and the limbic system after treatment with neuroleptic and anti-acetylcholine drugs

    J. Pharm. Pharmacol.

    (1972)
  • AsherI.M. et al.

    6-Hydroxydopamine lesions of olfactory tubercles and caudate nuclei: effect on amphetamine-induced stereotyped behaviour in rats

    Brain Research

    (1974)
  • CarrL.A. et al.

    Norepinephrine release from brain byd-amphetaminein vivo

    Science

    (1969)
  • CostallB. et al.

    Extrapyramidal and mesolimbic involvement with the stereotypic activity ofd- andl-amphetamine

    Europ. J. Pharmacol.

    (1974)
  • CreeseI. et al.

    Amphetamine response after dopamine neurone destruction

    Nature New Biol.

    (1972)
  • CreeseI. et al.

    Blockade of amphetamine induced motor stimulation and stereotypy in the adult rat following neonatal treatment with 6-hydroxydopamine

    Brain Research

    (1973)
  • CreeseI. et al.

    The role of forebrain dopamine systems in amphetamine induced stereotyped behaviour in the rat

    Psychopharmacologia (Berl.)

    (1974)
  • CreeseI. et al.

    The pharmacological and anatomical substrates of the amphetamine response in the rat

    Brain Research

    (1975)
  • CuelloA. et al.

    Use of catechol-O-methyltransferase for the enzyme radiochemical assay of dopamine

    J. Neurochem.

    (1973)
  • DivacI.

    Drug-induced syndromes in rats with large, chronic lesions in the corpus striatum

    Psychopharmacologia (Berl.)

    (1972)
  • ErnstA.M. et al.

    Site of action of dopamine and apomorphine on compulsive gnawing behaviour in rats

    Experientia (Basel)

    (1966)
  • FogR.

    On stereotypy and catalepsy: studies on the effect of amphetamine and neuroleptics in rats

    Acta neurol. scand.

    (1972)
  • GlowinskiJ. et al.

    Metabolism of norepinephrine in the central nervous system

    Pharmacol. Rev.

    (1966)
  • GlowinskiJ. et al.

    Regional studies of catecholamines in the rat brain

    J. Neurochem.

    (1966)
  • HollisterA.S. et al.

    Comparison of tyrosine hydroxylase and dopamine-β-hydroxylase inhibition with the effects of various 6-hydroxydopamine treatments andd-amphetamine induced motor activity

    Psychopharmacologia (Berl.)

    (1974)
  • HornA.S. et al.

    Dopamine in the mesolimbic system of the rat brain: endogenous levels and the effects of drugs on the uptake mechanism and stimulation of adenylate activity

    J. Neurochem.

    (1974)
  • KellyP.H. et al.

    Interaction of neuroleptic and muscarinic agents with central dopaminergic systems

    Brit. J. Pharmacol.

    (1975)
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