Amphetamine and apomorphine responses in the rat following 6-OHDA lesions of the nucleus accumbens septi and corpus striatum.
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Summary
Recovery of behavioural effects correlated with an increase in the remaining levels of DA in the NAS, and there is evidence that remaining DA levels in theNAS are greater at 90 than at 14 days postoperatively.
- Type
- article
- Published
- 1975-09-05
- Cited by
- 1,777
- References
- 30
- OpenAlex
- https://openalex.org/W2022395708
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:34146311
Keywords
Apomorphine, Amphetamine, Nucleus accumbens, Caudate nucleus, Dopamine
References
- Proceedings: Effect of aporphine alkaloids on central dopamine receptors.
- A stereotaxic atlas of the rat brain
- REGIONAL STUDIES OF CATECHOLAMINES IN THE RAT BRAIN‐I
- Involvement of nigro-striatal neurons in the in vivo release of dopamine by amphetamine, amantadine and tyramine.
- THE INTERACTION OF NEUROLEPTIC AND MUSCARINIC AGENTS WITH CENTRAL DOPAMINERGIC SYSTEMS
- Stereotype hyperactive behaviour produced by dopamine in the absence of noradrenaline.
- Extrapyramidal and mesolimbic involvement with the stereotypic activity of D- and L-amphetamine.
- DOPAMINE IN THE MESOLIMBIC SYSTEM OF THE RAT BRAIN: ENDOGENOUS LEVELS AND THE EFFECTS OF DRUGS ON THE UPTAKE MECHANISM AND STIMULATION OF ADENYLATE CYCLASE ACTIVITY
- The relative importance of dopaminergic and noradrenergic neuronal systems for the stimulation of locomotor activity induced by amphetamine and other drugs.
- Striatal dopamine release after amphetamine or nerve degeneration revealed by rotational behaviour.
- Norepinephrine: Release from Brain by d-Amphetamine in vivo
- EFFECTS OF 6‐HYDROXYDOPAMINE ON CATECHOLAMINE CONTAINING NEURONES IN THE RAT BRAIN
- Antagonism of D-amphetamine by alpha-methyl-L-tyrosine: behavioral evidence for the participation of catecholamine stores and synthesis in the amphetamine stimulant response.
- Role of Catecholamines in the Amphetamine Excitatory Response
- Stimulation of locomotor activity following injection of dopamine into the nucleus accumbens
- Postsynaptic supersensitivity after 6-hydroxy-dopamine induced degeneration of the nigro-striatal dopamine system.
- 6-Hydroxydopamine lesions of olfactory tubercles and caudate nuclei: effect on amphetamine-induced stereotyped behavior in rats.
- Use of catechol O‐methyltransferase for the enzyme radiochemical assay of dopamine
- Effects of substantia nigra lesions on the locomotor and stereotypy responses to amphetamine.
- Blockage of amphetamine induced motor stimulation and stereotypy in the adult rat following neonatal treatment with 6-hydroxydopamine.
Cited by
- Amphetamine-induced locomotor activity and stereotypy after kainic acid lesions of the striatum.
- Aporphines. 16. Action of aporphine alkaloids on locomotor activity in rats with 6-hydroxydopamine lesions of the nucleus accumbens.
- EVIDENCE CONCERNING THE INVOLVEMENT OF 5‐HYDROXYTRYPTAMINE IN THE LOCOMOTOR ACTIVITY PRODUCED BY AMPHETAMINE OR TRANYLCYPROMINE PLUS l‐DOPA
- Enhanced dopamine metabolism in accumbens leads to motor activity and concurrently to increased output from nondopamine neurons in ventral tegmental area and substantia nigra.
- AMPA/kainic acid glutamate receptor antagonism in the zona incerta dorsal to the subthalamic nucleus inhibits amphetamine-induced stereotypy bur not locomotor activity.
- Pharmacological study of TA-0910, a new thyrotropin-releasing hormone (TRH) analog (II): Involvement of the DA system in the locomotor stimulating action of TA-0910.
- Depletion of catecholamines in the brain of rats differentially affects stimulation of locomotor activity by caffeine, D-amphetamine, and methylphenidate.
- Similar post-lesion receptor readjustments following the unilateral 6-hydroxydopamine lesion of the dopaminergic mesotelencephalic system in neonatal and adult rats.
- Effects of chronic treatments with amineptine and despiramine on motor responses involving dopaminergic systems
- Altered central monoamine response tod-amphetamine in rats chronically exposed to inorganic lead
- Interactions between neuropeptides and dopamine neurons in the ventromedial mesencephalon.
- beta-Endorphin involvement in the antidopaminergic effect of caerulein.
- Influence of SCH 23390, a DA1-receptor antagonist, on the behavioural responsiveness to small and large doses of apomorphine in rats.
- Prolactin-induced yawning behavior requires an intact nigro-striatal dopamine system.
- Bilateral lesions of the striatum induced with 6-hydroxydopamine abolish apomorphine-induced yawning in rats.
- Selective disruption of displacement behaviour by lesions of the mesolimbic dopamine system
- Interaction of opiates with dopamine receptors: receptor binding and behavioral assays.
- Behavioural changes during withdrawal from desmethylimipramine (DMI)
- Magnitude and duration of hyperactivity following neonatal 6-hydroxydopamine is related to the extent of brain dopamine depletion
- Effects of lateral and medial septal lesions on exploratory behavior in the albino rat.
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