Department of Psychiatry, School of Medicine, University of California San Diego, 9500 Gilman Drive, M/C 0603, Room BSB2202, La Jolla, CA, 92093, USA.
Allergan, Jersey City, NJ, USA.
Psychopharmacology (Berl). 2018 May;235(5):1403-1414. doi: 10.1007/s00213-018-4857-0. Epub 2018 Feb 22.
Attentional processing deficits are a core feature of schizophrenia, likely contributing to the persistent functional and occupational disability observed in patients with schizophrenia. The pathophysiology of schizophrenia is hypothesized to involve dysregulation of NMDA receptor-mediated glutamate transmission, contributing to disruptions in normal dopamine transmission. Preclinical investigations often use NMDA receptor antagonists, such as phencyclidine (PCP), to induce cognitive disruptions relevant to schizophrenia. We sought to test the ability of partial dopamine D/D agonists, cariprazine and aripiprazole, to attenuate PCP-induced deficits in attentional performance.
The objective of this study is to determine whether systemic administration of cariprazine or aripiprazole attenuated 5-choice serial reaction time task (5-CSRTT) deficits induced by repeated exposure to PCP.
We utilized a repeated PCP-treatment regimen (2 mg/kg, subcutaneous [s.c.], once daily for 5 days) in rats to induce deficits in the 5-CSRTT. Rats were pre-treated with cariprazine (0.03, 0.1, or 0.3 mg/kg, oral [p.o.]) or aripiprazole (1, 3, or 10 mg/kg, p.o.) to determine whether they prevented PCP-induced deficits in the 5-CSRTT performance.
PCP treatment increased inappropriate responding in the 5-CSRTT, elevating incorrect, premature, and timeout responses. Cariprazine treatment reduced PCP-induced increases in inappropriate responding. However, at higher doses, cariprazine produced non-specific response suppression, confounding interpretation of the attenuated PCP-induced deficits. Aripiprazole treatment also attenuated PCP-induced deficits; however, unlike cariprazine treatment, aripiprazole reduced correct responding and increased omissions.
Cariprazine and aripiprazole both demonstrated potential in attenuating PCP-induced deficits in the 5-CSRTT performance. While both compounds produced non-specific response suppression, these effects were absent when 0.03 mg/kg cariprazine was administered.
注意力处理缺陷是精神分裂症的核心特征,可能导致精神分裂症患者持续存在功能和职业障碍。精神分裂症的病理生理学假设涉及 NMDA 受体介导的谷氨酸传递的失调,导致正常多巴胺传递的中断。临床前研究通常使用 NMDA 受体拮抗剂,如苯环利定(PCP),诱导与精神分裂症相关的认知障碍。我们试图测试部分多巴胺 D/D 激动剂,卡利拉嗪和阿立哌唑,减轻 PCP 诱导的注意力表现障碍的能力。
本研究的目的是确定系统给予卡利拉嗪或阿立哌唑是否减轻了反复暴露于 PCP 引起的 5-选择连续反应时间任务(5-CSRTT)缺陷。
我们使用重复 PCP 治疗方案(2mg/kg,皮下[sc],每天一次,共 5 天)在大鼠中诱导 5-CSRTT 缺陷。大鼠预先给予卡利拉嗪(0.03、0.1 或 0.3mg/kg,口服[p.o.])或阿立哌唑(1、3 或 10mg/kg,p.o.),以确定它们是否预防 PCP 诱导的 5-CSRTT 表现缺陷。
PCP 治疗增加了 5-CSRTT 中的不当反应,增加了不正确、过早和超时反应。卡利拉嗪治疗降低了 PCP 诱导的不当反应增加。然而,在较高剂量下,卡利拉嗪产生非特异性反应抑制,混淆了对减轻的 PCP 诱导缺陷的解释。阿立哌唑治疗也减轻了 PCP 诱导的缺陷;然而,与卡利拉嗪治疗不同,阿立哌唑降低了正确反应并增加了遗漏。
卡利拉嗪和阿立哌唑都显示出减轻 PCP 诱导的 5-CSRTT 表现缺陷的潜力。虽然两种化合物都产生了非特异性反应抑制,但当给予 0.03mg/kg 卡利拉嗪时,这些作用不存在。