Gujar Vaibhav V, Daiwile Atul P, Palande Vikrant, Cadet Jean Lud
Molecular Neuropsychiatry Research Branch, NIDA-IRP, NIH, Baltimore, MD, 21224, USA.
Department of Pathology, Johns Hopkins University, Baltimore, MD, USA.
Neurochem Int. 2025 Jul;187:105980. doi: 10.1016/j.neuint.2025.105980. Epub 2025 Apr 23.
Significant methamphetamine (METH)-induced behavioral differences exist between the two sexes of humans and other animals. These dissimilarities may be related to sexual dimorphism in baseline molecular and biochemical mechanisms in brain reward neuroanatomical pathways. As a first step towards identifying sex-based differences in methamphetamine-induced transcriptional signatures, we used RNA sequencing analysis to measure genome-wide changes in gene expression in the dorsal striatum of rats that had self-administered METH. We trained rats to self-administer METH (0.1 mg/kg/infusion, i.v.) using two 3-hr daily sessions (with 30 min time out between sessions) for 20 days. Control rats self-administered saline under similar conditions. This was followed by drug seeking tests on withdrawal days 3 (WD3) and 30 (WD30). Behavioral results show that male rats took more METH than female rats. In both male and female rats, some animals escalated (high-takers) whereas others did not escalate (low-takers) their METH intake during the behavioral experiment. Rats were euthanized 24 h after the second drug seeking test. RNA was extracted from the dorsal striatum (dSTR) and used in RNA sequencing analysis. The data identified substantial baseline differences in gene expression between female and male control rats. In addition, METH use and withdrawal were associated with significant sex-related differences in changes in striatal gene expression, with minimal overlaps of altered mRNAs. Thus, the present results provide further supporting evidence for sexually dimorphic responses to METH exposure. These observations support the notion of sex-specific approaches to the treatment of patients who suffer from METH use disorder.
在人类和其他动物的两性之间,存在显著的甲基苯丙胺(METH)诱导的行为差异。这些差异可能与大脑奖赏神经解剖通路中基线分子和生化机制的性别二态性有关。作为确定甲基苯丙胺诱导的转录特征中基于性别的差异的第一步,我们使用RNA测序分析来测量自行服用METH的大鼠背侧纹状体中基因表达的全基因组变化。我们训练大鼠使用每天两个3小时的时段(时段之间有30分钟休息时间)自行服用METH(0.1 mg/kg/注射,静脉注射),持续20天。对照大鼠在类似条件下自行服用生理盐水。随后在戒断第3天(WD3)和第30天(WD30)进行觅药测试。行为结果表明,雄性大鼠比雌性大鼠服用更多的METH。在雄性和雌性大鼠中,一些动物(高摄入者)在行为实验期间增加了METH摄入量,而另一些动物(低摄入者)则没有增加。在第二次觅药测试后24小时对大鼠实施安乐死。从背侧纹状体(dSTR)中提取RNA,并用于RNA测序分析。数据确定了雌性和雄性对照大鼠之间在基因表达上存在显著的基线差异。此外,使用METH和戒断与纹状体基因表达变化中显著的性别相关差异有关,改变的mRNA重叠极少。因此,本研究结果为对METH暴露的性别二态性反应提供了进一步的支持证据。这些观察结果支持针对患有METH使用障碍的患者采取性别特异性治疗方法的观点。