Department of Psychology, Center for Development and Behavioral Neuroscience, Binghamton University, Binghamton, NY, 13902, United States; Developmental Exposure Alcohol Research Center, Binghamton University, Binghamton, NY, 13902, United States.
Department of Psychology, Center for Development and Behavioral Neuroscience, Binghamton University, Binghamton, NY, 13902, United States; Developmental Exposure Alcohol Research Center, Binghamton University, Binghamton, NY, 13902, United States.
Neuropharmacology. 2021 May 15;189:108530. doi: 10.1016/j.neuropharm.2021.108530. Epub 2021 Mar 16.
Adolescents are phenotypically characterized with hyper-sensitivity to stress and inappropriate response to stress-inducing events. Despite behavioral distinctions from adults, investigations of developmental shifts in the function of stress peptide corticotropin-releasing factor (CRF) are generally limited. Rodent models have determined that CRF receptor 1 (CRFR1) activation within the central amygdala is associated with a stress response and induces increased GABAergic synaptic neurotransmission within adult males. To investigate age- and sex-specific function of this system, we performed whole-cell patch clamp electrophysiology in brain slices from naive adolescent (postnatal days (P) 40-49) and adult (>P70) male and female Sprague Dawley rats to assess GABAergic activity in the medial central amygdala (CeM). Our results indicate a dynamic influence of age and sex on neuronal excitability within this region, as well as basal spontaneous and miniature (m) inhibitory post-synaptic currents (IPSCs) in the CeM. In addition to replicating prior findings of CRFR1-regulated increases in mIPSC frequency in adult males, we found that the selective CRFR1 agonist, Stressin-1, attenuated mIPSC frequency in adolescent males, at a concentration that did not produce an effect in adult males. Importantly, this age-specific distinction was absent in females, as Stressin-1 attenuated mIPSC frequency in both adolescent and adult females. Finally, an increase in mIPSC frequency in response to the CRF1R antagonist, NBI 35965, was observed only in the CeM of adult males. Together, these data emphasize the robust influence of age and sex on neurophysiological function of a brain region involved in the production of the stress response.
青少年在应激反应方面表现出明显的高敏感性和对应激诱导事件的不适当反应。尽管与成年人的行为存在差异,但对发育过程中应激肽促肾上腺皮质释放因子 (CRF) 功能变化的研究通常受到限制。啮齿动物模型已经确定,中枢杏仁核内的 CRF 受体 1 (CRFR1) 激活与应激反应有关,并在成年雄性动物中诱导增加 GABA 能突触神经传递。为了研究该系统的年龄和性别特异性功能,我们在来自幼稚青少年(出生后第 40-49 天)和成年(>P70)雄性和雌性 Sprague Dawley 大鼠的脑片中进行全细胞膜片钳电生理学,以评估中中央杏仁核(CeM)中的 GABA 能活性。我们的结果表明,年龄和性别对该区域神经元兴奋性有动态影响,以及 CeM 中的基础自发和微小(m)抑制性突触后电流(IPSCs)。除了复制先前关于 CRFR1 调节成年雄性 mIPSC 频率增加的发现外,我们还发现选择性 CRFR1 激动剂 Stressin-1 可降低青少年雄性动物的 mIPSC 频率,而在成年雄性动物中,该浓度不会产生作用。重要的是,这种年龄特异性差异在雌性中不存在,因为 Stressin-1 降低了青少年和成年雌性的 mIPSC 频率。最后,仅在成年雄性动物的 CeM 中观察到 CRF1R 拮抗剂 NBI 35965 增加 mIPSC 频率。这些数据共同强调了年龄和性别对参与应激反应产生的脑区神经生理功能的强大影响。