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Oz Rokach, R.

Publications and source records attributed to Oz Rokach, R..

2 recordsLinked to original sources

'What' and 'where' brain-wide pathways are dominated by internal strategies

It is long thought that higher-order sensory processing is divided into two specialized cortical streams that encode in parallel either the identity of an object or its location (i.e., what and where streams). Here, using the mouse whisker system, we challenge this concept by demonstrating an existence of two alternating brain-wide (beyond cortex) subnetworks that are not primarily driven by external parameters, but rather by internal strategies. We combine simultaneous brain-wide neuronal recordings in mice trained to identify or locate a certain stimulus. We find that mice deploy either an active search or a passive sensation strategy during task performance. These strategies respectively drive two distinct and brain-wide subnetworks, frontal and posterior, regardless of the type of task performed. The posterior subnetwork encoded additional internal strategic parameters such as trial history, the first task of the day, and training history. A subgroup of trials that were not dominated by frontal cortex, contained meaningful task information in the posterior cortex and several thalamic areas. Integrated together, these two subnetworks may comprise normal cognitive function.

neuroscience↗

Aberrant circuitry underlying olfaction in the face of severe olfactory bulb degeneration

The olfactory bulb (OB) is a critical component of mammalian olfactory neuroanatomy. Beyond being the first and sole relay station for olfactory information to the rest of the brain, it also contains elaborate stereotypical circuitry that is considered essential for olfaction. Indeed, substantial lesions of the OB in rodents lead to anosmia. Here, we examined the circuitry that underlies olfaction in a mouse model with severe developmental degeneration of the OB. These mice could perform odor-guided tasks and even responded normally to innate olfactory cues. Despite the near total loss of the OB, piriform cortex in these mice responded to odors normally and its neural activity sufficed to decode odor identity. We analyzed the circuitry that supports olfactory function in these mice. We found that sensory neurons express the full repertoire of olfactory receptors and their axons project primarily to the rudimentary OB, but also ectopically, to olfactory cortical regions. Within the OB, the number of principal neurons was greatly reduced and the morphology of their dendrites was abnormal, extending over larger regions within the OB. Glomerular organization was lost. This study shows that olfactory functionality can be preserved despite reduced and aberrant circuitry that is missing many of the elements that are believed to be essential for olfaction, and may explain the retention of olfaction in humans with degenerated OBs.

neuroscience↗