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. 2014 Nov;38(11):2770-9.
doi: 10.1111/acer.12555.

Social isolation rearing increases nucleus accumbens dopamine and norepinephrine responses to acute ethanol in adulthood

Affiliations

Social isolation rearing increases nucleus accumbens dopamine and norepinephrine responses to acute ethanol in adulthood

Anushree N Karkhanis et al. Alcohol Clin Exp Res. 2014 Nov.

Abstract

Background: Early-life stress is associated with increased vulnerability to alcohol addiction. However, the neural substrates linking chronic childhood/adolescent stress and increased risk of alcohol addiction are not well understood. In the nucleus accumbens (NAc), dopamine (DA) and norepinephrine (NE) signaling can be profoundly influenced by stress, anxiety, and drugs of abuse, including ethanol (EtOH). Here, we employed a rodent model of early-life stress that results in enduring increases in behavioral risk factors of alcoholism to gain a better understanding of how chronic adolescent stress may impact the EtOH sensitivity of DA and NE release in the NAc.

Methods: Male Long-Evans rats were either group housed (GH; 4 rats/cage) or socially isolated (SI; 1 rat/cage) for 6 weeks beginning on postnatal day 28. SI and GH rats were tested in adulthood for anxiety-like behaviors (elevated plus maze), and the effects of EtOH (1 and 2 g/kg; intraperitoneally.) on NAc DA and NE were assessed by microdialysis.

Results: SI animals showed increased anxiety-like behavior compared to GH animals. Although SI had no effect on baseline levels of DA or NE, baseline DA levels were positively correlated with anxiety measures. In addition, while no significant differences were observed with 1 g/kg EtOH, the 2 g/kg dose induced significantly greater DA release in SI animals. Moreover, EtOH (2 g/kg) only elevated NAc NE levels in SI rats.

Conclusions: These results suggest that chronic early-life stress sensitizes accumbal DA and NE release in response to an acute EtOH challenge. A greater EtOH sensitivity of DA and NE release dynamics in the NAc may contribute to increases in behavioral risk factors of alcoholism, like greater EtOH self-administration, that are observed in SI rats.

Keywords: Dopamine; Ethanol; Norepinephrine; Nucleus Accumbens; Social Isolation.

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Figures

Figure 1
Figure 1
A schematic of the experimental paradigm. Male, Long Evans rats arrived at the facility on postnatal day (PD 21) and were maintained in group housing to acclimate for one week. On PD 28, half the rats were housed individually while the other half remained in group housing. The behavioral testing was conducted on PD 74 and microdialysis experiments were conducted between PD 80 and 110. EPM, elevated plus maze.
Figure 2
Figure 2
Coronal sections showing microdialysis probe locations. Microdialysis probes were inserted in the NAc using the Paxinos and Watson (2007) rat atlas.
Figure 3
Figure 3
An elevated plus maze (EPM) was used to phenotype for anxiety-like behavior in SI (n=17) and GH (n=15) rats. (A) Time spent on the open arm of the EPM. SI rats spent significantly less amount of time on the open arm compared to GH rats indicating increased anxiety-like behavior. (B) SI rats demonstrated fewer numbers of entries onto the open arm compared to GH rats exemplifying increased anxiety-like behavior. (C) No significant difference in number of closed arm entries was observed between SI and GH rats implying that locomotion was not affected due to the social isolation paradigm. GH, group housed; SI, socially isolated; **, p < 0.01.
Figure 4
Figure 4
Blood EtOH elimination curves. Blood samples collected from tails of SI (n=7) and GH (n=7) animals showed that there was no significant difference in the clearance of EtOH. GH, group housed; SI, socially isolated
Figure 5
Figure 5
EtOH-induced DA response in the NAc of SI and GH rats. (A) Baseline levels of DA in SI (n=17) and GH (n=15) were not significantly different. DA concentrations were corrected for concentrations in the dialysate. (B) A significant positive correlation was observed between DA levels at baseline and anxiety-like behavior. Increased anxiety was associated with higher levels of DA. A significant positive correlation was observed within the GH animals, but no significant correlation was observed within the SI animals, potentially due to a floor effect for the number of open arm entries. (C) An EtOH dose comparison within the GH animals showed that the two doses of EtOH had comparable effects on DA release in the NAc. (D) An EtOH dose comparison within the SI animals demonstrated that at a higher dose (2 g/kg), acute EtOH resulted in an augmentation of the DA response in the NAc. (E) A two-way ANOVA between housing and dose comparison showed that social isolation results in an augmentation of EtOH-induced DA release only at a higher dose (2 g/kg) of EtOH and only in SI animals, confirming that both housing and dose affected DA responses to EtOH. (F) Saline comparison between GH and SI animals showed that saline did not significantly elevate DA levels in either group. SI, socially isolated; GH, group housed; *, p < 0.05; **, p < 0.01; ***, p < 0.001 (1 g/kg vs. 2 g/kg); #, p < 0.05; ##, p < 0.01; ###, p < 0.001 (post-EtOH DA response vs. baseline). GH, group housed; SI, socially isolated. GH: 1 g/kg EtOH, n=9; 2 g/kg EtOH, n=8; saline, n=7. SI: 1 g/kg EtOH, n=9; 2 g/kg EtOH, n=9; saline, n=8.
Figure 6
Figure 6
EtOH-induced NE response in the NAc of SI and GH animals. (A) Extracellular levels of NE at baseline in the NAc of SI (n=8) and GH (n=8) animals. Social isolation did not significantly alter the extracellular levels of NE in the NAc. NE concentrations were corrected for concentrations in the dialysate. (B) A dose comparison within the GH rats did not show a significant difference in 1 and 2 g/kg EtOH dose. (C) Acute EtOH (2 g/kg but not 1 g/kg) resulted in an augmentation of NE release in the SI animals. (D) A two-way ANOVA of dose and housing effects on the EtOH-induced NE response showed that a higher dose of EtOH (2 g/kg) induced increased NE response in the SI animals. (E) Saline comparison between GH and SI animals showed that saline administration did not significantly elevate NE levels in either group. SI, socially isolated; GH, group housed; *, p < 0.05; **, p < 0.01; ***, p < 0.001 (1 g/kg vs. 2 g/kg); #, p < 0.05 (post-EtOH DA response vs. baseline). GH, group housed; SI, socially isolated. EtOH 1 and 2 g/kg: SI and GH, n=6 in all groups; saline: GH, n=6; SI, n=4.

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