Psychology Department, Otago University, Dunedin 9054, New Zealand.
Psychology Department, University of Sheffield, Sheffield, United Kingdom.
J Neurosci. 2022 May 18;42(20):4187-4201. doi: 10.1523/JNEUROSCI.0039-22.2022. Epub 2022 Apr 8.
Spatial memory and reward processing are known to be disrupted in schizophrenia. Since the lateral septum (LS) may play an important role in the integration of location and reward, we examined the effect of maternal immune activation (MIA), a known schizophrenia risk factor, on spatial representation in the rat LS. In support of a previous study, we found that spatial location is represented as a phase code in the rostral LS of adult male rats, so that LS cell spiking shifts systematically against the phase of the hippocampal, theta-frequency, local field potential as an animal moves along a track toward a reward (phase precession). Whereas shallow precession slopes were observed in control group cells, they were steeper in the MIA animals, such that firing frequently precessed across several theta cycles as the animal moved along the length of the apparatus, with subsequent ambiguity in the phase representation of location. Furthermore, an analysis of the phase trajectories of the control group cells revealed that the population tended to converge toward a common firing phase as the animal approached the reward location. This suggested that phase coding in these cells might signal both reward location and the distance to reward. By comparison, the degree of phase convergence in the MIA-group cells was weak, and the region of peak convergence was distal to the reward location. These findings suggest that a schizophrenia risk factor disrupts the phase-based encoding of location-reward relationships in the LS, potentially smearing reward representations across space. It is unclear how spatial or contextual information generated by hippocampal cells is converted to a code that can be used to signal reward location in regions, such as the VTA. Here we provide evidence that the firing phase of cells in the lateral septum, a region that links the two areas, may code reward location in the firing phase of cells. This phase coding is disrupted in a maternal immune activation model of schizophrenia risk such that representations of reward may be smeared across space in maternal immune activation animals. This could potentially underlie erroneous reward processing and misattribution of salience in schizophrenia.
空间记忆和奖励处理在精神分裂症中已知会受到干扰。由于外侧隔核(LS)可能在位置和奖励的整合中发挥重要作用,我们研究了母体免疫激活(MIA),一种已知的精神分裂症风险因素,对大鼠 LS 中空间表示的影响。支持之前的一项研究,我们发现空间位置在成年雄性大鼠 LS 的前颅侧以相位码表示,因此 LS 细胞的爆发随着动物沿着轨迹向奖励移动,与海马体、θ 频率的相位系统地移动,局部场电位(相位超前)。虽然在对照组细胞中观察到浅的超前斜率,但在 MIA 动物中斜率更陡,使得随着动物沿着仪器的长度移动,发射经常超前几个θ 周期,从而导致位置的相位表示出现后续歧义。此外,对对照组细胞相位轨迹的分析表明,随着动物接近奖励位置,群体倾向于向共同的发射相位收敛。这表明这些细胞中的相位编码可能同时信号奖励位置和距离奖励。相比之下,MIA 组细胞的相位收敛程度较弱,并且峰值收敛区域位于奖励位置的远端。这些发现表明,一种精神分裂症风险因素会破坏 LS 中位置-奖励关系的基于相位的编码,可能会在空间中模糊奖励表示。尚不清楚海马体细胞产生的空间或上下文信息如何转换为可用于在 VTA 等区域指示奖励位置的代码。在这里,我们提供的证据表明,连接两个区域的外侧隔核细胞的发射相位可能在细胞的发射相位中对奖励位置进行编码。这种相位编码在精神分裂症风险的母体免疫激活模型中受到破坏,使得奖励的表示在母体免疫激活动物中可能在空间上模糊。这可能是精神分裂症中错误的奖励处理和显着性错误归因的基础。