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Long-term administration of d-amphetamine: Progressive augmentation of motor activity and stereotypy

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TLDR
carry-over of both the post-injection augmentation and dark phase reduction of locomotion was revealed during amphetamine retest 8 days following discontinuation of daily d-amphetamine injections, indicating the importance of their concurrent evaluation, especially during chronic studies.
Abstract
The competitive relationship between d-amphetamine induced stereotypy and locomotor activity indicates the importance of their concurrent evaluation, especially during chronic studies. Repeated injection of 0.5, 1.0, 2.5, 5.0, or 7.5 mg/kg d-amphetamine for 36 successive days, in rats continuously exposed to the experimental chambers, produced a progressive augmentation in stereotypy and/or locomotion (depending on dose) during the 3–4 hr interval following injections (post-injection phase). In contrast, dark phase locomotor activity (8–20 hr after each daily injection) was maximally reduced (30–40% of controls) after the first injection of either 5.0 or 7.5 mg/kg d-amphetamine and gradually declined to this level with repeated injection of 1.0 and 2.5 mg/kg. Carry-over of both the post-injection augmentation and dark phase reduction of locomotion was revealed during amphetamine retest 8 days following discontinuation of daily d-amphetamine injections. Possible mechanisms underlying these behavioral alterations are discussed.

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Journal ArticleDOI

Stages of constant amphetamine intoxication: Delayed appearance of abnormal social behaviors in rat colonies

TL;DR: This late phase of constant amphetamine intoxication in rats has a number of similarities to amphetamine psychosis in humans, and can serve as a useful animal model for the study of its biochemical correlates.
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A dopaminergic mechanism is involved in the 'anxiogenic-like' response induced by chronic amphetamine treatment: a behavioral and neurochemical study.

TL;DR: Previous exposure to chronic AMPH treatment induces an increased emotional response following a conflict situation, and dopamine D(1) receptors are mainly involved in chronicAMPH-induced changes in the behavior displayed in EPM test, suggesting an interaction between GABAergic and dopaminergic mechanisms may be implicated in neurochemical and behavioral changes induced by chronic AM PH treatment.
Journal ArticleDOI

Effects of drug experience on drug induced conditioned taste aversions: studies with amphetamine and fenfluramine.

TL;DR: Conditioned taste aversions established in rats to 0.1% sodium saccharin by intra-peritoneal injections of dl-fenfluramine hydrochloride or d-amphetamine sulphate were found to be significantly attenuated, but not abolished altogether, by chronic pretreatment with the specific drug.
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Lasting effects of repeated ∆9‐tetrahydrocannabinol vapour inhalation during adolescence in male and female rats

TL;DR: Growing legalization of cannabis for medical and recreational purposes, combined with decreasing perceptions of harm, makes it increasingly important to determine the consequences of frequent adolescent exposure for motivated behaviour and lasting tolerance in response to THC.
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Dissociation between long-lasting behavioral sensitization to amphetamine and impulsive choice in rats performing a delay-discounting task

TL;DR: The results suggest that one behavioral consequence of repeated AMPH exposure—sensitization—does not overlap with another potential outcome—increased impulsivity, and the neuroadaptations known to be associated with sensitization may be somewhat distinct from those that lead to changes in impulsive choice.
References
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Journal Article

Antiamphetamine effects following inhibition of tyrosine hydroxylase

TL;DR: The antiamphetamine effects of α-MT and other tyrosine hydroxylase inhibitors suggest that a critical level of norepinephrine at the receptor is required for amphetamine to exert its customary effects.
Journal ArticleDOI

Role of Catecholamines in the Amphetamine Excitatory Response

A. Randrup, +1 more
- 30 Jul 1966 - 
TL;DR: The advent of α-methyl para-tyrosine3 (α-MPT), which inhibits the in vivo synthesis of 3,4-dihydroxyphenylalanine (DOPA)—the physiological precursor of the catecholamines—offers a new way of investigating this problem.
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