Cocaine abstinence following chronic treatment alters cerebral metabolism in dopaminergic reward regions. Bromocriptine enhances recovery
Description
2-[14C]deoxyglucose autoradiography was used to determine local cerebral glucose utilization (lCGU) in rats following chronic cocaine treatment and subsequent abstinence. lCGU was examined in 43 discrete brain regions in animals which had received daily injections of cocaine for 14 days (10 mg/kg) followed by 3 days of saline or bromocriptine (10 mg/kg) treatment. Cocaine abstinence following chronic treatment significantly reduced lCGU in several regions including mesocorticolimbic structures such as ventral tegmental area, medial prefrontal cortex, and nucleus accumbens (NAc). Within the NAc, however, only the rostral pole showed significant reduction. In contrast, when bromocriptine treatment accompanied abstinence, lCGU was no longer reduced in mesocorticolimbic and most other regions, implying that metabolic recovery was enhanced by bromocriptine treatment during early abstinence following chronic cocaine treatment. These data suggest that cerebral metabolism is decreased during cocaine abstinence following chronic treatment in critical brain regions, and that this alteration can be prevented by treatment with direct-acting dopamine agonists such as bromocriptine
Additional details
Publishing Information
- Journal Title
- Neuropsychopharmacology
- Journal Volume
- 4
- Journal Issue
- 1
- Series
- Neuropsychopharmacology.
- Journal Page Range
- 71-75
- ISSN
- 0893-133X
- CODEN
- NEROE
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 22051041
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- AUTORADIOGRAPHY; BIOCHEMICAL REACTION KINETICS; BIOLOGICAL EFFECTS; CARBON 14 COMPOUNDS; CEREBRAL CORTEX; COCAINE; DOPAMINE; ENZYME INHIBITORS; GLUCOSE; METABOLISM; RATS
- Descriptors DEC
- ALDEHYDES; ALKALOIDS; AMINES; ANESTHETICS; ANIMALS; ANTIDEPRESSANTS; AROMATICS; AUTONOMIC NERVOUS SYSTEM AGENT; BODY; BRAIN; CARBOHYDRATES; CARBON COMPOUNDS; CARDIOTONICS; CARDIOVASCULAR AGENTS; CENTRAL NERVOUS SYSTEM; CENTRAL NERVOUS SYSTEM AGENTS; CENTRAL NERVOUS SYSTEM DEPRESS; CEREBRUM; DRUGS; HEXOSES; HYDROXY COMPOUNDS; KINETICS; MAMMALS; MONOSACCHARIDES; NERVOUS SYSTEM; NEUROREGULATORS; ORGANIC COMPOUNDS; ORGANS; PHENOLS; POLYPHENOLS; PSYCHOTROPIC DRUGS; REACTION KINETICS; RODENTS; SACCHARIDES; SYMPATHOMIMETICS; VERTEBRATES