Molecular Neuropsychiatry Research Branch, NIDA Intramural Research Program, Baltimore, MD 21224, United States.
Molecular Neuropsychiatry Research Branch, NIDA Intramural Research Program, Baltimore, MD 21224, United States.
Neuroscience. 2021 Jan 1;452:265-279. doi: 10.1016/j.neuroscience.2020.11.025. Epub 2020 Nov 24.
Sex differences in METH use exist among human METH users and in animal models of METH addiction. Herein, we tried to identify potential differences in gene expression between female and male rats after Methamphetamine self-administration (METH SA). Rats were trained to self-administer METH using two 3-hours daily sessions for 20 days. Cue-induced drug seeking was measured on withdrawal days 3 (WD3) and 30 (WD30). Rats were euthanized twenty-four hours after WD30. Prefrontal cortex (PFC) and hippocampus (HIP) were dissected to measure mRNA expression. Both female and male rats increased their METH intake and showed increased METH seeking during withdrawal. Female had higher basal level expression of hypocretin receptor 1 (Hcrtr1) and prodynorphin (Pdyn) mRNAs in the PFC and HIP. Basal corticotropin releasing hormone receptor 1 (Crhr1), Crh receptor 2 (Crhr2), hypocretin receptor 2 (Hcrtr2) and opioid receptor kappa 1 (Oprk1) mRNA levels were higher in the PFC of females. Male rats had higher basal levels of Crh and Crhr1 in HIP. METH SA was associated with increased Crh and Crhr1 in the HIP of both sexes and Crhr2 only in female HIP. Importantly, increased Crh and Crhr1 mRNA levels correlated positively with incubation of METH craving in both sexes, supporting their potential involvement, in part, in the regulation of this behavioral phenomenon. When taken together, our results identified sexual dimorphic baseline differences in rats. We also detected dimorphic responses in animals that had self-administered METH. These observations highlight the importance of understanding the molecular neurobiology of sex differences when therapeutic interventions are planned against METH addiction.
在人类冰毒使用者和冰毒成瘾的动物模型中,存在性别差异。在此,我们试图确定雄性和雌性大鼠在接受冰毒自我给药(METH SA)后基因表达的潜在差异。大鼠接受了为期 20 天的每天 2 次 3 小时的冰毒自我给药训练。在戒断第 3 天(WD3)和第 30 天(WD30)测量线索诱导的觅药行为。在 WD30 后 24 小时处死大鼠。从前额叶皮层(PFC)和海马(HIP)中分离出 mRNA 表达。雌雄大鼠均增加了冰毒摄入量,并在戒断期间增加了冰毒觅药。雌性大鼠 PFC 和 HIP 中的下丘脑分泌素受体 1(Hcrtr1)和前原啡肽(Pdyn)mRNA 的基础表达水平较高。雌性大鼠 PFC 中的促肾上腺皮质激素释放激素受体 1(Crhr1)、CRH 受体 2(Crhr2)、下丘脑分泌素受体 2(Hcrtr2)和阿片受体 kappa 1(Oprk1)mRNA 水平较高。雄性大鼠 HIP 中的 CRH 和 Crhr1 基础水平较高。METH SA 与两性 HIP 中 CRH 和 Crhr1 的增加有关,仅在雌性 HIP 中与 Crhr2 增加有关。重要的是,冰毒觅药潜伏期的增加与两性 CRH 和 Crhr1 mRNA 水平呈正相关,这支持了它们在调节这种行为现象中的潜在作用。总的来说,我们的研究结果确定了雄性和雌性大鼠之间存在性别差异的基线差异。我们还在接受过 METH 自我给药的动物中检测到了性别差异的反应。这些观察结果强调了在计划针对 METH 成瘾的治疗干预时,了解性别差异的分子神经生物学的重要性。