Department of Psychology, 238 Burnett Hall, University of Nebraska-Lincoln, Lincoln, NE 68588-0308, USA.
Pharmacol Biochem Behav. 2012 Dec;103(2):174-80. doi: 10.1016/j.pbb.2012.08.021. Epub 2012 Aug 31.
Olanzapine is one of the most widely prescribed atypical antipsychotic drugs in the treatment of schizophrenia. Besides its well-known side effect on weight gain, it may also impair human parental behavior. In this study, we took a preclinical approach to examine the behavioral effects of olanzapine on rat maternal behavior and investigated the associated neural basis using the c-Fos immunohistochemistry. On postpartum days 6-8, Sprague-Dawley mother rats were given a single injection of sterile water or olanzapine (1.0, 3.0 or 5.0mg/kg, sc). Maternal behavior was tested 2h later, after which rats were sacrificed and brain tissues were collected. Ten brain regions that were either implicated in the action of antipsychotic drugs and/or in the regulation of maternal behavior were examined for c-Fos immunoreactivity. Acute olanzapine treatment dose-dependently disrupted various components of maternal behavior (e.g., pup retrieval, pup licking, nest building, crouching) and increased c-Fos immunoreactivity in the medial prefrontal cortex (mPFC), nucleus accumbens shell and core (NAs and NAc), dorsolateral striatum (DLSt), ventral lateral septum (LSv), central amygdala (CeA) and ventral tegmental area (VTA), important brain areas generally implicated in the incentive motivation and reward processing. In contrast, olanzapine treatment did not alter c-Fos in the medial preoptic nucleus (MPN), ventral bed nucleus of the stria terminalis (vBST) and medial amygdala (MeA), the core brain areas directly involved in the mediation of rat maternal behavior. These findings suggest that olanzapine disrupts rat maternal behavior primarily by suppressing incentive motivation and reward processing via its action on the mesocorticolimbic dopamine systems, other limbic and striatal areas, but not by disrupting the core processes involved in the mediation of maternal behavior in particular.
奥氮平是治疗精神分裂症最广泛使用的非典型抗精神病药物之一。除了众所周知的体重增加副作用外,它还可能损害人类的父母行为。在这项研究中,我们采用临床前方法研究了奥氮平对大鼠母性行为的行为影响,并使用 c-Fos 免疫组织化学法研究了相关的神经基础。产后第 6-8 天,给予 Sprague-Dawley 母鼠单次注射无菌水或奥氮平(1.0、3.0 或 5.0mg/kg,sc)。2 小时后测试母性行为,然后处死大鼠并收集脑组织。检查了 10 个脑区的 c-Fos 免疫反应性,这些脑区要么与抗精神病药物的作用有关,要么与母性行为的调节有关。急性奥氮平治疗剂量依赖性地破坏了母性行为的各种成分(例如,幼崽回收、幼崽舔舐、筑巢、蹲伏),并增加了内侧前额叶皮层(mPFC)、伏隔核壳和核心(NAs 和 NAc)、背外侧纹状体(DLSt)、腹外侧隔核(LSv)、中央杏仁核(CeA)和腹侧被盖区(VTA)的 c-Fos 免疫反应性,这些脑区通常与激励动机和奖励处理有关。相比之下,奥氮平治疗并未改变内侧视前核(MPN)、腹侧终纹床核(vBST)和内侧杏仁核(MeA)中的 c-Fos,这些脑区是直接参与调节大鼠母性行为的核心脑区。这些发现表明,奥氮平通过其对中脑边缘多巴胺系统、其他边缘和纹状体区域的作用,主要通过抑制激励动机和奖励处理来破坏大鼠的母性行为,而不是通过破坏与母性行为调节特别相关的核心过程。