Long-term cognitive impairments induced by chronic cannabinoid exposure during adolescence in rats: a strain comparison

Psychopharmacology (Berl). 2013 Feb;225(4):781-90. doi: 10.1007/s00213-012-2865-z. Epub 2012 Sep 16.

Abstract

Rationale: During cerebral development, adolescence is a critical phase in which the endocannabinoid system plays an important role in regulating various neurotransmitters. Moreover, evidence from both human and animal studies suggests that chronic cannabinoid exposure during this vulnerable period can induce persistent brain and behavioural alterations.

Objectives: The aim of this study was to compare the long-term cognitive consequences of chronic adolescence cannabinoid exposure between Lister Hooded rats and Wistar rats.

Methods: Rats of both strains were injected daily throughout their adolescent or adult periods with vehicle or with incremental doses of the synthetic cannabinoid CB1 receptor agonist CP55,940 (CP). Short-term and spatial working memories were assessed using the object recognition and object location, tasks respectively. For both tasks, the effect of a 30- or 120-min delay between the learning and the testing phase was investigated.

Results: In the object recognition task, adolescent CP exposure impaired short-term memory after both delays in both strains. In contrast, in the object location task, adolescent CP exposure impaired spatial working memory in the Wistar rats after a 30-min delay, whereas the Lister Hooded rats exhibited a similar effect only after a 120-min delay. In these tests, no long-term deleterious effects were found following adult CP exposure in either strain.

Conclusions: Our results confirm that adolescence is a critical period for the deleterious effects of cannabinoids on cognition and that these deleterious effects on spatial working memory are more strain-dependent than the effects observed on short-term memory.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Cannabinoids / administration & dosage
  • Cannabinoids / toxicity*
  • Cognition Disorders / chemically induced*
  • Cognition Disorders / genetics*
  • Cyclohexanols / administration & dosage
  • Cyclohexanols / toxicity*
  • Male
  • Memory, Short-Term / drug effects*
  • Memory, Short-Term / physiology*
  • Rats
  • Rats, Wistar
  • Spatial Behavior / drug effects
  • Spatial Behavior / physiology
  • Species Specificity
  • Time Factors

Substances

  • Cannabinoids
  • Cyclohexanols
  • 3-(2-hydroxy-4-(1,1-dimethylheptyl)phenyl)-4-(3-hydroxypropyl)cyclohexanol