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Dissimilar patterns of degeneration in brain following four different addictive stimulants.

G Ellison, R C Switzer

Neuroreport October 25, 1993 DOI: 10.1097/00001756-199310000-00004 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Animal study Peer reviewed
Population Rats
Interventions D-amphetamine cocaine phencyclidine methamphetamine
Duration 5-day period for D-amphetamine, cocaine, and phencyclidine; high-dose but less prolonged regimen for methamphetamine
Key points Drugs of abuse with psychotomimetic properties induce distinctively different patterns of neural degeneration, with D-amphetamine and cocaine affecting the fasciculus retroflexus, PCP affecting the posterior entorhinal cortex and related regions, and methamphetamine causing widespread damage.

Abstract

Patterns of neural degeneration were compared following continuous administration of four drugs of addiction, each of which induces model psychoses in chronic addicts. D-amphetamine (D-Amph), cocaine (Coc), or phencyclidine (PCP) were administered continuously over a 5-day period. Both D-Amph and Coc induced pronounced degeneration in fasciculus retroflexus, but only D-Amph further induced substantial degeneration in striatum. Continuous PCP produced entirely different degeneration largely confined to the posterior entorhinal cortex, ventral dentate gyrus, and cingulate cortex. Methamphetamine (Meth) administered in the very high dose but less prolonged drug regimen often employed in studies of dopamine toxicity induced pronounced degeneration in striatum, but widespread degeneration in many other regions as well. These results indicate that drugs of abuse with psychotomimetic properties induce distinctively different patterns of neural degeneration, a finding with implications for theories of addiction and psychosis. They predict two different anatomical loci for alterations in psychosis: fasciculus retroflexus and ventral parahippocampus and hippocampus.

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