Electrophysiological properties of the medial mammillary bodies across the sleep-wake cycle

Abstract

AbstractThe medial mammillary bodies (MB) play an important role in the formation of spatial memories. Dense anatomical connectivity with hippocampal, brainstem, and thalamic structures, positions them as a focal point for the integration of movement-related and spatial information that is extended to the anterior thalamic nuclei and beyond to cortex. While their anatomical connectivity has been well-studied, much less is known about the physiological properties of the medial MBs, particularly in freely moving animals. We therefore carried out a comprehensive characterization of medial MB electrophysiology across arousal states by concurrently recording from the medial MB and the CA1 field of the hippocampus. In agreement with previous studies, we found medial MB neurons to have firing rates modulated by running speed and angular head velocity, as well as theta-entrained firing. We extended the characterization of MB neuron electrophysiology in three key ways: 1) we identified a subset of neurons (25%) that exhibit dominant bursting activity; 2) we show that ∼30% of theta-entrained neurons exhibit robust theta cycle skipping, a firing characteristic that implicates them in a network for prospective coding of position; 3) A considerable proportion of medial MB units show sharp wave-ripple (SWR) responsive firing (∼37%). The functional heterogeneity of MB electrophysiology reinforces their role as an integrative node for mnemonic processing and identifies potential roles for the MBs in memory consolidation through propagation of SWR-responsive activity to the anterior thalamus and prospective coding in the form of theta-cycle skipping.Significance StatementWhile the medial mammillary bodies (MBs) are important for memory, it is still not clear how they support memory formation. Through conjoint medial MB and hippocampal recordings across different arousal states we identified a population of medial MB units with diverse and often conjunctive physiological properties, including theta-entrained cells, cells modulated by running speed and angular head velocity, complex bursting, theta cycle skipping activity, and hippocampal sharp-wave ripple-responsive firing. These properties likely support a role for the medial MBs in mnemonic processing, enabling the integration of separate sensory streams and the propagation of information to the thalamus.