Aug 2026· The Journal of comparative neurology· Vol 534· 0 citations· 67 references
Medicine
TL;DR
These findings provide the first detailed map of the hindlimb sensorimotor cortex in spiny mice, establishing a crucial neuroanatomical foundation for future studies using this novel model in sensorimotor research.
Abstract
The Cairo spiny mouse (Acomys cahirinus), a promising animal model in neuroscience, lacks a detailed neuroanatomical map of its cerebral cortex. This study aims to delineate the location and internal subdivision of the sensorimotor cortex, specifically the region controlling the hindlimb. For this purpose, retrograde tracing from the lumbar spinal cord using Fast Blue was combined with immunohistochemical characterization using neuronal markers (NeuN, SMI‐32, and calbindin 28 kDa) in adult animals. Fast Blue‐labeled neurons were identified in layer V within the cortical region defined as the sensorimotor cortex responsible for hindlimb control. Within this region, the general cytoarchitecture was defined using NeuN, which allowed visualization of all cortical layers. The border between the lateral and medial sub‐areas was clearly identified by SMI‐32 immunostaining, which showed denser labeling in the lateral zone (presumably the primary somatosensory cortex) compared to the medial zone (presumably the secondary motor cortex). Within the defined layers and sub‐areas, a comprehensive analysis of the calbindin‐expressing interneuron population was performed, revealing significant interareal differences in soma size and cellular density of calbindin‐positive neurons exclusively within layers III–IV. These findings provide the first detailed map of the hindlimb sensorimotor cortex in spiny mice, establishing a crucial neuroanatomical foundation for future studies using this novel model in sensorimotor research.
Findings support region‐specific specialization of inhibitory interneuron organization in the human prefrontal cortex and suggest that differences in supragranular inhibitory circuitry may contribute to the distinct functional architecture of dorsal and ventral prefrontal cortico‐cortical networks.
Ivan Banovac, M. Baković, Davor Mayer et al.· Journal of Anatomy· 0 citations
The main finding was the identifi cation of a rostrocaudal gradient of connectivity in which the more the authors move from cranial to caudal body representation areas in Ml, the more the corresponding connected area in the medial wall is shifted rostrocaudally, confirming the somatotopic schema found in the SMA.
F. Cauda, '’ D ’Agata Federico Geminiani Giuliano, D. Sergio et al.· 8 citations
OBJECTIVE
The striate cortex (V1) and the adjacent area prostriata (Pro) are key components of visual cortical organization. In the domestic cat, however, the cytoarchitectural and chemoarchitectural features of the medial V1-presubiculum (Prs) transition remain incompletely defined, and the anatomical relationship bet...
Da Chen, Jun-Jie Liu, Cairu Li et al.· Brain Research· 0 citations
The current manuscript aims to provide a more complete data set that can used to delineate the dorsal, intermediate, and ventral divisions of the posterior ectosylvian gyrus (auditory cortical regions dPE, iPE, and vPE, respectively) based on SMI-32 reactivity using the same methods and measures.
Austin Robertson, Jeffrey G. Mellott, Blake E. Butler· bioRxiv· 0 citations
This manuscript addresses key considerations for sensorimotor exploration in both pediatric and adult clinical settings and proposes a three-dimensional, patient-tailored exploration of sensorimotor circuits that more closely reflects individual anatomy and network organization.
Ammar Kheder, P. Jain· Journal of clinical neurophy...· 0 citations
Progressive, age-dependent remodeling of motor cortex somatotopic remodeling is demonstrated in 5XFAD mice, characterized by early expansion of specific simple movement cortical sites followed by deterioration of both complex and simple motor cortical maps as disease advances.
SE Moss, Cassandra C. Wolsh, Rmii Brown et al.· bioRxiv· 0 citations
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