Pharmacology Department, University of Michigan, Ann Arbor, MI, USA.
Neuroscience Graduate Program, University of California, Berkeley, CA, USA.
Biol Sex Differ. 2023 Jun 24;14(1):41. doi: 10.1186/s13293-023-00525-8.
The development and persistence of addiction is mediated in part by drug-induced alterations in nucleus accumbens (NAc) function. AMPA-type glutamate receptors (AMPARs) provide the main source of excitatory drive to the NAc and enhancements in transmission of calcium-permeable AMPARs (CP-AMPARs) mediate increased cue-triggered drug-seeking following prolonged withdrawal. Cocaine treatment regimens that result in psychomotor sensitization enhance subsequent drug-seeking and drug-taking behaviors. Furthermore, cocaine-induced locomotor sensitization followed by 14 days of withdrawal results in an increase in glutamatergic synaptic transmission. However, very few studies have examined cocaine-induced alterations in synaptic transmission of females or potential effects of experimenter-administered cocaine on NAc CP-AMPAR-mediated transmission in either sex.
Male and female rats were given repeated systemic cocaine injections to induce psychomotor sensitization (15 mg/kg, i.p. 1 injection/day, 8 days). Controls received repeated saline (1 mL/kg, i.p). After 14-16 days of withdrawal brain slices were prepared and whole-cell patch-clamp approaches in the NAc core were used to measure spontaneous excitatory post-synaptic currents (sEPSC), paired pulse ratio, and CP-AMPAR transmission. Additional female rats from this same cohort were also given a challenge injection of cocaine at withdrawal day 14 to assess the expression of sensitization.
Repeated cocaine produced psychomotor sensitization in both sexes. In males this was accompanied by an increase in sEPSC frequency, but not amplitude, and there was no effect on the paired pulse ratio. Males treated with cocaine and saline had similar sensitivity to Naspm. In contrast, in females there were no significant differences between cocaine and saline groups on any measure, despite females showing robust psychomotor sensitization both during the induction and expression phase.
Overall, these data reveal striking sex differences in cocaine-induced NAc glutamate plasticity that accompany the induction of psychomotor sensitization. This suggests that the neural adaptations that contribute to sensitization vary by sex.
成瘾的发展和持续部分是由药物引起的伏隔核(NAc)功能改变介导的。AMPA 型谷氨酸受体(AMPAR)为 NAc 提供了主要的兴奋性驱动力,而钙通透性 AMPAR(CP-AMPAR)的传递增强介导了长期戒断后线索触发的药物寻求增加。导致精神运动敏化的可卡因治疗方案增强了随后的药物寻求和药物摄入行为。此外,可卡因诱导的运动敏化后再进行 14 天的戒断会导致谷氨酸能突触传递增加。然而,很少有研究检查过可卡因对女性 NAc CP-AMPAR 介导的传递的突触传递的改变,或实验者给予可卡因对两性中 NAc CP-AMPAR 介导的传递的潜在影响。
雄性和雌性大鼠接受重复的全身可卡因注射以诱导精神运动敏化(15mg/kg,腹腔内 1 次/天,8 天)。对照组接受重复的盐水(1ml/kg,腹腔内)。在 14-16 天的戒断后,制备脑切片,并在 NAc 核心中使用全细胞贴片钳技术测量自发性兴奋性突触后电流(sEPSC)、成对脉冲比和 CP-AMPAR 传递。来自同一队列的其他雌性大鼠也在戒断日 14 给予可卡因挑战注射,以评估敏化的表达。
重复可卡因在两性中均产生精神运动敏化。在雄性中,这伴随着 sEPSC 频率的增加,但幅度没有增加,对成对脉冲比没有影响。接受可卡因和盐水治疗的雄性对 Naspm 的敏感性相似。相比之下,在雌性中,尽管在诱导和表达阶段,雌性都表现出强烈的精神运动敏化,但在任何测量中,可卡因组和盐水组之间都没有显著差异。
总的来说,这些数据揭示了可卡因诱导的 NAc 谷氨酸可塑性存在显著的性别差异,这伴随着精神运动敏化的诱导。这表明导致敏化的神经适应因性别而异。