Details

Autor(en) / Beteiligte

• Areal, Lorena B.
• Rodrigues, Livia C.M.
• Andrich, Filipe
• Moraes, Livia S.
• Cicilini, Maria A.
• Mendonça, Josideia B.
• Pelição, Fabricio S.
• Nakamura-Palacios, Ester M.
• Martins-Silva, Cristina
• Pires, Rita G.W.

Titel

Behavioural, biochemical and molecular changes induced by chronic crack-cocaine inhalation in mice: The role of dopaminergic and endocannabinoid systems in the prefrontal cortex

Ist Teil von

• Behavioural brain research, 2015-09, Vol.290, p.8-16

Ort / Verlag

Netherlands: Elsevier B.V

Erscheinungsjahr

2015

Quelle

MEDLINE

Beschreibungen/Notizen

• •We investigated changes in the prefrontal cortex of mice exposed to crack-cocaine inhalation.•The crack-cocaine group exhibited hyperlocomotion and an exclusive jumping behaviour.•Most genes related to the endocannabinoid system were downregulated in crack-cocaine mice.•Dopamine levels were decreased and their receptors were upregulated after drug exposure.•It suggests that both systems are involved in the mechanism of addiction to this drug. Crack-cocaine addiction has increasingly become a public health problem worldwide, especially in developing countries. However, no studies have focused on neurobiological mechanisms underlying the severe addiction produced by this drug, which seems to differ from powder cocaine in many aspects. This study investigated behavioural, biochemical and molecular changes in mice inhaling crack-cocaine, focusing on dopaminergic and endocannabinoid systems in the prefrontal cortex. Mice were submitted to two inhalation sessions of crack-cocaine a day (crack-cocaine group) during 11 days, meanwhile the control group had no access to the drug. We found that the crack-cocaine group exhibited hyperlocomotion and a peculiar jumping behaviour (“escape jumping”). Blood collected right after the last inhalation session revealed that the anhydroecgonine methyl ester (AEME), a specific metabolite of cocaine pyrolysis, was much more concentrated than cocaine itself in the crack-cocaine group. Most genes related to the endocannabinoid system, CB1 receptor and cannabinoid degradation enzymes were downregulated after 11-day crack-cocaine exposition. These changes may have decreased dopamine and its metabolites levels, which in turn may be related with the extreme upregulation of dopamine receptors and tyrosine hydroxylase observed in the prefrontal cortex of these animals. Our data suggest that after 11 days of crack-cocaine exposure, neuroadaptive changes towards downregulation of reinforcing mechanisms may have taken place as a result of neurochemical changes observed on dopaminergic and endocannabinoid systems. Successive changes like these have never been described in cocaine hydrochloride models before, probably because AEME is only produced by cocaine pyrolysis and this metabolite may underlie the more aggressive pattern of addiction induced by crack-cocaine.