Nash Family Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Department of Genetics and Genomic Sciences and Icahn Institute for Data Science and Genomic Technology, Icahn School of Medicine at Mount Sinai, New York, New York; Mount Sinai Center for Transformative Disease Modeling, Icahn School of Medicine at Mount Sinai, New York, New York.
Biol Psychiatry. 2022 Jan 1;91(1):118-128. doi: 10.1016/j.biopsych.2021.02.964. Epub 2021 Feb 24.
Sex differences in addiction have been described in humans and animal models. A key factor that influences addiction in both males and females is adolescent experience. Adolescence is associated with higher vulnerability to substance use disorders, and male rodents subjected to adolescent social isolation (SI) stress form stronger preferences for drugs of abuse in adulthood. However, little is known about how females respond to SI, and few studies have investigated the transcriptional changes induced by SI in the brain's reward circuitry.
We tested the hypothesis that SI alters the transcriptome in a persistent and sex-specific manner in prefrontal cortex, nucleus accumbens, and ventral tegmental area. Mice were isolated or group housed from postnatal day P22 to P42, then group housed until ∼P90. Transcriptome-wide changes were investigated by RNA sequencing after acute or chronic cocaine or saline administration.
We found that SI disrupts sex-specific transcriptional responses to cocaine and reduces sex differences in gene expression across all three brain regions. Furthermore, SI induces gene expression profiles in males that more closely resemble group-housed females, suggesting that SI "feminizes" the male transcriptome. Coexpression analysis reveals that such disruption of sex differences in gene expression alters sex-specific gene networks and identifies potential sex-specific key drivers of these transcriptional changes.
Together, these data show that SI has region-specific effects on sex-specific transcriptional responses to cocaine and provide a better understanding of reward-associated transcription that differs in males and females.
人类和动物模型都描述了成瘾中的性别差异。影响男性和女性成瘾的一个关键因素是青少年经历。青春期与更高的物质使用障碍易感性有关,雄性啮齿动物在青春期经历社会隔离(SI)应激后,成年后对滥用药物的偏好更强。然而,对于女性如何对 SI 做出反应知之甚少,并且很少有研究调查 SI 对大脑奖励回路中诱导的转录变化。
我们测试了这样一个假设,即 SI 以持久和性别特异性的方式改变前额叶皮层、伏隔核和腹侧被盖区中的转录组。从出生后第 22 天到第 42 天,将小鼠隔离或群体饲养,然后直到大约第 90 天进行群体饲养。急性或慢性可卡因或生理盐水给药后,通过 RNA 测序研究转录组的广泛变化。
我们发现 SI 破坏了可卡因对性别特异性转录反应的影响,并减少了三个脑区中性别差异的基因表达。此外,SI 诱导了雄性中更类似于群体饲养雌性的基因表达谱,这表明 SI“女性化”了雄性转录组。共表达分析表明,这种性别差异的基因表达的破坏改变了性别特异性基因网络,并确定了这些转录变化的潜在性别特异性关键驱动因素。
总之,这些数据表明 SI 对可卡因对性别特异性转录反应具有区域特异性影响,并提供了对男性和女性不同的奖励相关转录的更好理解。