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Influence of the anabolic-androgenic steroid nandrolone on cannabinoid dependence.

Evelyne Célérier, Therese Ahdepil, Helena Wikander, Fernando Berrendero, Fred Nyberg, Rafaël Maldonado

Neuropharmacology June 2006 DOI: 10.1016/j.neuropharm.2005.11.017 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical experimental study in mice Peer reviewed
Population Mice
Interventions Nandrolone Delta(9)-tetrahydrocannabinol (THC) rimonabant (SR141617A)
Duration Nandrolone pre-exposure for 14 days before THC treatment; nandrolone co-administration 1 hour before each THC injection
Measures conditioned place preference, somatic withdrawal signs, antinociception, hypothermia, hypolocomotion, lit/dark box, open field, elevated plus-maze, CB1 receptor binding, GTP-binding protein activation
Topics Addiction
Key findings Chronic nandrolone treatment in mice blocked THC- and food-induced conditioned place preference and increased somatic signs of rimonabant-precipitated THC withdrawal, while leaving THC's acute effects, tolerance, and aversive effects unchanged. Nandrolone pre-exposure also attenuated the anxiolytic-like effect of a low THC dose without altering the anxiogenic-like effect of a high dose. The authors suggest these behavioral changes relate to cannabinoid addictive properties.

Abstract

The identification of the possible factors that might enhance the risk of developing drug addiction and related motivational disorders is crucial to reduce the prevalence of these problems. Here, we examined in mice whether the exposure to the anabolic-androgenic steroid nandrolone would affect the pharmacological and motivational effects induced by Delta(9)-tetrahydrocannabinol (THC), the principal psychoactive component of Cannabis sativa. Mice received nandrolone using pre-exposure (during 14days before THC treatment) or co-administration (1h before each THC injection) procedures. Both nandrolone treatments did not modify the acute antinociceptive, hypothermic and hypolocomotor effects of THC or the development of tolerance after chronic THC administration. Nandrolone pre-exposure blocked THC- and food-induced conditioned place preference and increased the somatic manifestations of THC withdrawal precipitated by the CB1 cannabinoid antagonist rimonabant (SR141617A). The aversive effects of THC were not changed by nandrolone. Furthermore, nandrolone pre-exposure attenuated the anxiolytic-like effects of a low dose of THC without altering the anxiogenic-like effects of a high dose in the lit/dark box, open field and elevated plus-maze. Biochemical experiments showed that chronic nandrolone treatment did not modify CB1 receptor binding and GTP-binding protein activation in the caudate-putamen and cerebellum. Taken together, our results suggest that chronic nandrolone treatment alters behavioural responses related to cannabinoid addictive properties.

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