OCD-Like behaviors caused by a neuropotentiating transgene targeted to cortical and limbic D1+ neurons.

Published

Journal Article

To study the behavioral role of neurons containing the D1 dopamine receptor (D1+), we have used a genetic neurostimulatory approach. We generated transgenic mice that express an intracellular form of cholera toxin (CT), a neuropotentiating enzyme that chronically activates stimulatory G-protein (Gs) signal transduction and cAMP synthesis, under the control of the D1 promoter. Because the D1 promoter, like other CNS-expressed promoters, confers transgene expression that is regionally restricted to different D1+ CNS subsets in different transgenic lines, we observed distinct but related psychomotor disorders in different D1CT-expressing founders. In a D1CT line in which transgene expression was restricted to the following D1+ CNS regions-the piriform cortex layer II, layers II-III of somatosensory cortical areas, and the intercalated nucleus of the amygdala-D1CT mice showed normal CNS and D1+ neural architecture but increased cAMP content in whole extracts of the piriform and somatosensory cortex. These mice also exhibited a constellation of compulsive behavioral abnormalities that strongly resembled human cortical-limbic-induced compulsive disorders such as obsessive-compulsive disorder (OCD). These compulsive behaviors included episodes of perseverance or repetition of any and all normal behaviors, repetitive nonaggressive biting of siblings during grooming, and repetitive leaping. These results suggest that chronic potentiation of cortical and limbic D1+ neurons thought to induce glutamatergic output to the striatum causes behaviors reminiscent of those in human cortical-limbic-induced compulsive disorders.

Full Text

Duke Authors

Cited Authors

  • Campbell, KM; de Lecea, L; Severynse, DM; Caron, MG; McGrath, MJ; Sparber, SB; Sun, LY; Burton, FH

Published Date

  • June 15, 1999

Published In

Volume / Issue

  • 19 / 12

Start / End Page

  • 5044 - 5053

PubMed ID

  • 10366637

Pubmed Central ID

  • 10366637

Electronic International Standard Serial Number (EISSN)

  • 1529-2401

Language

  • eng

Conference Location

  • United States