1978
DOI: 10.1126/science.26975
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Long-Term Changes in Dopaminergic Innervation of Caudate Nucleus After Continuous Amphetamine Administration

Abstract: Silicone pellets containing d-amphetamine base were implanted subcutaneously in rats. These pellets release amphetamine continuously for at least 10 days. Several days after implantation, swollen dopamine axons concomitant with large decreases in tyrosine hydroxylase activity were observed in the caudate nucleus. Decreased tyrosine hydroxylase activity was still present 110 days after pellet removal in the caudate but not in several other brain regions, nor in the caudate of rats injected with an equivalent am… Show more

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Cited by 305 publications
(79 citation statements)
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“…Cytosolic dopamine is then released to the extracellular space via reverseͲ transport by the DAT. Amphetamine also interferes with dopamine metabolism by inhibiting MAO [293], and with dopamine synthesis, by inhibiting TH [294].Thus, longͲterm exposure to amphetamine leads to dopamine depletion [295], and reduction in dopaminergic markers [296].…”
Section: Amphetaminesdopamine and Pdmentioning
confidence: 99%
“…Cytosolic dopamine is then released to the extracellular space via reverseͲ transport by the DAT. Amphetamine also interferes with dopamine metabolism by inhibiting MAO [293], and with dopamine synthesis, by inhibiting TH [294].Thus, longͲterm exposure to amphetamine leads to dopamine depletion [295], and reduction in dopaminergic markers [296].…”
Section: Amphetaminesdopamine and Pdmentioning
confidence: 99%
“…At low concentrations, amphetamine promotes dopamine synthesis (Kuczenski, 1975), whereas at higher concentrations or upon prolonged exposure, it leads to tyrosine hydroxylase (TH) inhibition (Ellison et al, 1978) or decreased TH protein levels (Bowyer et al, 1998). Amphetamine also impairs dopamine metabolism by inhibiting monoamine oxidase (MAO) (Ramsay and Hunter, 2002).…”
Section: Short-term Neurochemical Effectsmentioning
confidence: 99%
“…Indeed, chronic amphetamine treatment in rats is well-documented to be toxic to dopamine nerve terminals. 54 A reduction in dopamine could result in postsynaptic receptor supersensitivity, which would explain the re-emergence of positive symptoms after transiently increased dopamine availability, as occurs during stress or exposure to dopaminergic drugs.…”
Section: Clinical Experience With Stimulants: Support For the Dopaminmentioning
confidence: 99%