Department of Pharmacology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Departments of Neuroscience, Psychiatry, and Psychology, University of Pittsburgh, Pittsburgh, PA, USA.
Schizophr Bull. 2023 Jan 3;49(1):68-77. doi: 10.1093/schbul/sbac106.
Stress during adolescence is a major risk factor for schizophrenia. We have found previously in rats that adolescent stress caused, in adulthood, behavioral changes and enhanced ventral tegmental area (VTA) dopamine system activity, which were associated with dysregulation of the excitatory-inhibitory (E/I) balance in the ventral hippocampus (vHip). Levetiracetam, an anticonvulsant drug, regulates the release of neurotransmitters, including glutamate, via SV2A inhibition. It also modulates parvalbumin interneuron activity via Kv3.1 channels. Therefore, levetiracetam could ameliorate deficits in the E/I balance. We tested whether levetiracetam attenuate the adolescent stress-induced behavioral changes, vHip hyperactivity, and enhanced VTA dopamine system activity in adult rats.
Male Sprague-Dawley rats were subjected to a combination of daily footshock (postnatal day [PD] 31-40), and three 1 h-restraint stress sessions (at PD31, 32, and 40). In adulthood (PD62), animals were tested for anxiety responses (elevated plus-maze and light-dark box), social interaction, and cognitive function (novel object recognition test). The activity of vHip pyramidal neurons and VTA dopamine neurons was also recorded.
Adolescent stress produced anxiety-like responses and impaired sociability and cognitive function. Levetiracetam (10 mg/kg) reversed these changes. Levetiracetam also reversed the increased VTA dopamine neuron population activity and the enhanced firing rate of vHip pyramidal neurons induced by adolescent stress.
These findings suggest that levetiracetam attenuates the adverse outcomes associated with schizophrenia caused by stress during adolescence.
青少年时期的压力是精神分裂症的一个主要风险因素。我们之前在大鼠中发现,青春期压力会导致成年后行为改变和腹侧被盖区(VTA)多巴胺系统活性增强,这与腹侧海马(vHip)兴奋性-抑制性(E/I)平衡失调有关。左乙拉西坦是一种抗惊厥药物,通过 SV2A 抑制调节神经递质包括谷氨酸的释放。它还通过 Kv3.1 通道调节 Parvalbumin 中间神经元的活性。因此,左乙拉西坦可以改善 E/I 平衡的缺陷。我们测试了左乙拉西坦是否可以减轻青春期应激引起的成年大鼠行为改变、vHip 过度兴奋和 VTA 多巴胺系统活性增强。
雄性 Sprague-Dawley 大鼠接受每日足底电击(出生后第 31-40 天)和 3 次 1 小时束缚应激(在第 31、32 和 40 天)。在成年期(第 62 天),动物进行焦虑反应(高架十字迷宫和明暗箱)、社交互动和认知功能(新物体识别测试)测试。还记录了 vHip 锥体神经元和 VTA 多巴胺神经元的活动。
青春期应激产生了类似焦虑的反应,并损害了社交能力和认知功能。左乙拉西坦(10mg/kg)逆转了这些变化。左乙拉西坦还逆转了青春期应激引起的 VTA 多巴胺神经元群体活性增加和 vHip 锥体神经元放电率增强。
这些发现表明,左乙拉西坦减轻了青春期应激引起的与精神分裂症相关的不良后果。