Gonzalez Ivette L, Becker Jill B
Department of Psychology, University of Michigan.
Michigan Neuroscience Institute, University of Michigan.
bioRxiv. 2025 Feb 26:2025.02.25.640103. doi: 10.1101/2025.02.25.640103.
Dopamine (DA) is a neurotransmitter that is important in the reward system and increased DA release is associated with rewarding properties of drugs. Highly addictive stimulants like methamphetamine (METH) increase DA release and block reuptake, causing the DA to stay in the synapse longer, enhancing its effects. Because the misuse of METH is increasing in the United States, it is important to investigate ways to protect against this highly addictive stimulant. Recent studies have shown that social support can be a protective factor against METH self-administration in females, but not males. Other studies using microdialysis have shown that socially housed females have lower DA release in the nucleus accumbens (NAc) compared to single housed females after treatment with METH. Additionally, researchers have shown that there are sex differences in stimulated DA release. The present study investigates whether social housing affects stimulated DA release after METH treatment. DA release in the NAc core and shell of socially housed and individually housed rats was measured using fast scan cyclic voltammetry (FSCV) with a chronic 16-channel carbon fiber electrode in the NAc. A stimulating electrode was aimed at the ventral tegmental area (VTA) to induce DA release in the NAc. The results showed that social housing enhances electrically stimulated DA release in males and that there was greater DA release in NAc core than shell in single males, but no difference in socially housed males. In females, social housing also enhanced ES DA release. In single females there was greater ES DA release in shell than in core. Additionally, in single housed females there was greater ES DA release over time, while the socially housed females had high ES DA release that remained stable over time. These results suggest that social housing protects females from sensitization, making single females more vulnerable to the addictive properties of METH.
多巴胺(DA)是一种在奖赏系统中起重要作用的神经递质,多巴胺释放增加与药物的奖赏特性相关。像甲基苯丙胺(METH)这样的高成瘾性兴奋剂会增加多巴胺的释放并阻止其再摄取,使多巴胺在突触中停留更长时间,增强其作用。由于甲基苯丙胺在美国的滥用情况日益增加,研究预防这种高成瘾性兴奋剂的方法很重要。最近的研究表明,社会支持可以成为女性甲基苯丙胺自我给药的保护因素,但对男性则不然。其他使用微透析的研究表明,与单独饲养的雌性相比,群居雌性在接受甲基苯丙胺治疗后伏隔核(NAc)中的多巴胺释放较低。此外,研究人员表明,刺激引起的多巴胺释放存在性别差异。本研究调查群居是否会影响甲基苯丙胺治疗后刺激引起的多巴胺释放。使用快速扫描循环伏安法(FSCV)和NAc中的慢性16通道碳纤维电极测量群居和单独饲养大鼠的NAc核心和壳中的多巴胺释放。一个刺激电极对准腹侧被盖区(VTA)以诱导NAc中的多巴胺释放。结果表明,群居增强了雄性电刺激引起的多巴胺释放,并且单独饲养的雄性NAc核心中的多巴胺释放比壳中更多,但群居雄性中没有差异。在雌性中,群居也增强了电刺激引起的多巴胺释放。在单独饲养的雌性中,壳中的电刺激引起的多巴胺释放比核心中更多。此外,在单独饲养的雌性中,随着时间的推移电刺激引起的多巴胺释放更多,而群居雌性的电刺激引起的多巴胺释放较高且随时间保持稳定。这些结果表明,群居可保护雌性免受致敏,使单独饲养的雌性更容易受到甲基苯丙胺成瘾特性的影响。