Keck Center for the Neurobiology of Learning and Memory, Department of Neurobiology and Anatomy, McGovern Medical School at The University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.
MD Anderson UTHealth Graduate School of Biomedical Sciences, Houston, Texas 77030, USA.
Learn Mem. 2020 May 15;27(6):236-249. doi: 10.1101/lm.051367.120. Print 2020 Jun.
Operant reward learning of feeding behavior in increases the frequency and regularity of biting, as well as biases buccal motor patterns (BMPs) toward ingestion-like BMPs (iBMPs). The engram underlying this memory comprises cells that are part of a central pattern generating (CPG) circuit and includes increases in the intrinsic excitability of identified cells B30, B51, B63, and B65, and increases in B63-B30 and B63-B65 electrical synaptic coupling. To examine the ways in which sites of plasticity (individually and in combination) contribute to memory expression, a model of the CPG was developed. The model included conductance-based descriptions of cells CBI-2, B4, B8, B20, B30, B31, B34, B40, B51, B52, B63, B64, and B65, and their synaptic connections. The model generated patterned activity that resembled physiological BMPs, and implementation of the engram reproduced increases in frequency, regularity, and bias. Combined enhancement of B30, B63, and B65 excitabilities increased BMP frequency and regularity, but not bias toward iBMPs. Individually, B30 increased regularity and bias, B51 increased bias, B63 increased frequency, and B65 decreased all three BMP features. Combined synaptic plasticity contributed primarily to regularity, but also to frequency and bias. B63-B30 coupling contributed to regularity and bias, and B63-B65 coupling contributed to all BMP features. Each site of plasticity altered multiple BMP features simultaneously. Moreover, plasticity loci exhibited mutual dependence and synergism. These results indicate that the memory for operant reward learning emerged from the combinatoric engagement of multiple sites of plasticity.
在中操作奖励学习增加了进食行为的频率和规律性,并使口腔运动模式(BMPs)偏向于类似摄食的 BMPs(iBMPs)。这种记忆的记忆痕迹由中央模式生成(CPG)回路的一部分组成,包括鉴定细胞 B30、B51、B63 和 B65 的固有兴奋性增加,以及 B63-B30 和 B63-B65 电突触耦合增加。为了研究可塑性部位(单独和组合)对记忆表达的贡献方式,开发了一个 CPG 模型。该模型包括细胞 CBI-2、B4、B8、B20、B30、B31、B34、B40、B51、B52、B63、B64 和 B65 的基于电导率的描述及其突触连接。该模型产生的模式活动类似于生理 BMPs,并且记忆痕迹的实现再现了频率、规律性和偏差的增加。B30、B63 和 B65 兴奋性的联合增强增加了 BMP 的频率和规律性,但没有增加偏向 iBMPs 的趋势。单独的 B30 增加了规律性和偏差,B51 增加了偏差,B63 增加了频率,B65 降低了所有三种 BMP 特征。联合突触可塑性主要有助于规律性,但也有助于频率和偏差。B63-B30 耦合有助于规律性和偏差,而 B63-B65 耦合有助于所有 BMP 特征。每个可塑性部位同时改变了多个 BMP 特征。此外,可塑性部位表现出相互依赖和协同作用。这些结果表明,操作性奖励学习的记忆源自多个可塑性部位的组合参与。