Artigo
Temporal and Behavioral Variability in Cannabinoid Receptor Expression in Outbred Mice Submitted to Ethanol-Induced Locomotor Sensitization Paradigm
Fecha
2013-09-01Registro en:
Alcoholism-clinical and Experimental Research. Hoboken: Wiley-Blackwell, v. 37, n. 9, p. 1516-1526, 2013.
0145-6008
10.1111/acer.12130
WOS:000323676600010
Autor
Coelhoso, Cassia C. [UNIFESP]
Engelke, Douglas S. [UNIFESP]
Filev, Renato [UNIFESP]
Silveira, Dartiu X. [UNIFESP]
Mello, Luiz E. [UNIFESP]
Santos-Junior, Jair G. [UNIFESP]
Institución
Resumen
Background There is a close relationship between the endocannabinoid system and alcoholism. This study investigated possible differential expression of cannabinoid receptors CB1 (CB1R) and CB2 (CB2R) in an outbred mice strain displaying behavioral variability to ethanol (EtOH)-induced locomotor sensitization.Methods Male adult Swiss mice treated chronically with EtOH (2g/kg, i.p., daily for 21days) were classified as EtOH_High or EtOH_Low according to their locomotor activity after the 21st EtOH injection. A control group was similarly injected with saline. Temporal analysis of CB1R and CB2R immunoreactivity was performed in 3 different occasions: (i) at the end of chronic EtOH treatment, (ii) on the fifth day of EtOH withdrawal, and (iii) after EtOH challenge.Results Overall, no differences were seen between experimental groups regarding the CB1R at the end of acquisition. However, there were decreases in CB2R in the prefrontal cortex and the hippocampus in EtOH_Low mice. On the fifth day of withdrawal, only EtOH_High mice presented increase in CB1R. Nonetheless, CB2R up-regulation was observed in both EtOH_High and EtOH_Low mice. EtOH challenge counteracted CB1R and CBR2 up-regulation, mainly in the EtOH_High, in structures related to emotionality, such as prefrontal cortex, ventral tegmental area, amygdala, striatum, and hippocampus.Conclusions There are different patterns of cannabinoid receptor expression during locomotor sensitization paradigm, at both temporal and behavioral perspectives. We hypothesize that CB2R down-regulation might be related to resilience to develop locomotor sensitization, while CB1R up-regulation relates to withdrawal aspects in sensitized mice.
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