Department of Physiology, University of Saskatchewan, GD30.7, Health Sciences Building, 107 Wiggins Road, Saskatoon, SK, S7N 5E5, Canada.
Michael Smith Laboratories and Djavad Mowafaghian Centre for Brain Health, University of British Colombia, Vancouver, BC, Canada.
Psychopharmacology (Berl). 2018 Nov;235(11):3339-3350. doi: 10.1007/s00213-018-5040-3. Epub 2018 Sep 24.
Currently available antipsychotics are unsatisfactory given their side effects and limited efficacy for the cognitive symptoms of schizophrenia. Many currently available drugs, such as haloperidol, are T-type calcium channel antagonists in addition to their well-established antagonism of dopamine D2 receptors. Thus, preclinical research into the effects of T-type calcium channel antagonists/blockers in behavioral assays related to schizophrenia may inform novel therapeutic strategies.
We explored the effects of a recently developed highly selective T-type calcium channel antagonist, Z944 (2.5, 5.0, 10.0 mg/kg), on the MK-801 (0.15 mg/kg) model of acute psychosis.
To examine the effects of Z944 on behaviors relevant to schizophrenia, we tested touchscreen-based paired associates learning given its relevance to the cognitive symptoms of the disorder and locomotor activity given its relevance to the positive symptoms.
Acute treatment with Z944 failed to reverse the visuospatial associative memory impairments caused by MK-801 in paired associates learning. The highest dose of drug (10.0 mg/kg) given alone produced subtle impairments on paired associates learning. In contrast, Z944 (5.0 mg/kg) blocked the expected increase in locomotion following MK-801 treatment in a locomotor assay.
These experiments provide support that Z944 may reduce behaviors relevant to positive symptoms of schizophrenia, although additional study of its effects on cognition is required. These findings and other research suggest T-type calcium channel antagonists may be an alternative to currently available antipsychotics with less serious side effects.
鉴于目前抗精神病药物的副作用和对精神分裂症认知症状的疗效有限,它们的效果并不令人满意。许多现有的药物,如氟哌啶醇,除了其对多巴胺 D2 受体的明确拮抗作用外,还是 T 型钙通道拮抗剂。因此,针对 T 型钙通道拮抗剂/阻滞剂在与精神分裂症相关的行为测定中的作用的临床前研究可能为新的治疗策略提供信息。
我们研究了一种新开发的高选择性 T 型钙通道拮抗剂 Z944(2.5、5.0、10.0mg/kg)对 MK-801(0.15mg/kg)急性精神病模型的影响。
为了研究 Z944 对与精神分裂症相关的行为的影响,我们测试了基于触摸屏的配对联想学习,因为它与该疾病的认知症状有关,以及运动活动,因为它与阳性症状有关。
急性给予 Z944 未能逆转 MK-801 引起的视空间联想记忆障碍在配对联想学习中。单独给予最高剂量的药物(10.0mg/kg)会导致轻微的配对联想学习障碍。相比之下,Z944(5.0mg/kg)在运动测定中阻断了 MK-801 治疗后预期的运动增加。
这些实验支持 Z944 可能减少与精神分裂症阳性症状相关的行为,尽管需要进一步研究其对认知的影响。这些发现和其他研究表明,T 型钙通道拮抗剂可能是一种替代目前副作用较小的抗精神病药物的选择。