bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.06.24.731406

Spatial Distribution of Cortical Output Zones Affecting Combinations of Forelimb Muscles in the Monkey

Abstract

SUMMARY AND CONCLUSIONSO_LIWe investigated the dimensions of output zones affecting specific combinations of forelimb muscles in the precentral "motor" cortex of macaque monkeys. Single-pulse intracortical microstimulation (S-ICMS) was used to evoke subthreshold effects in multiple wrist and finger muscles. S-ICMS consisted of 15 Hz stimulus trains at low intensity (5 A) to avoid spread of effects due to temporal summation and to activate circumscribed foci of cortical cells in the bank of the precentral gyrus. C_LIO_LITo detect subthreshold effects on active muscles, stimuli were delivered during wrist movements against elastic loads, and stimulus-triggered averages of rectified electromyographic (EMG) activity of 12 identified forelimb muscles were compiled. These averages detected statistical increases and decreases in averaged rectified EMG activity termed poststimulus facilitation and poststimulus suppression, respectively (7, 8). The "muscle profile" of a cortical output site was defined as the distribution and relative magnitude of these effects evoked in the recorded muscles. To document the spatial extent of a cortical output zone producing a particular "muscle profile," we delivered S-ICMS at successive sites along electrode tracks in the precentral bank, tangential to and near layer V cells. C_LIO_LIIn some cases the electrodes encountered cortical cells whose post-spike effects on muscles were also documented by spike-triggered averages of EMG activity. Near cells that had post-spike effects, S-ICMS evoked a similar profile of effects on these muscles, over distances of several hundred microns from the location of the cells with post-spike output effects. C_LIO_LIThe locations of tracks were marked by electrolytic lesions at specific depths and were identified in subsequent histological reconstructions. The physiological effects evoked from different sites were correlated with the locations of Nissl-stained cortical cells and corticospinal cells labeled by horseradish peroxidase (HRP) transported from the cervical spinal cord. C_LIO_LIThe "muscle profiles" of poststimulus effects elicited by 5-10 A S-ICMS applied at successive sites were the same for multiple neighboring sites extending over tangential distances of about 1 mm. S-ICMS applied at 300 to 500 m intervals evoked significant poststimulus facilitation or suppression effects over a range of 650-1250 m. Assuming an effective excitation radius of 65 m for 5-A current pulses, the lower limit of the mean tangential dimension of cortical output zones on the precentral bank (n = 17) was estimated to be 800 m. C_LIO_LIA specific muscle could be affected, either singly or in combination with synergist muscles, from aggregate regions of output sites extending about 5 x 4 mm mediolateral x dorsoventral. These regions were comparable in size to output areas containing all the corticomotoneuronal (CM) cells that produced postspike facilitation in that muscle. C_LIO_LIThe cortical entry points of tracks with CM cells producing postspike facilitation in specific muscles were reconstructed for three monkeys. In two monkeys, the flexor and extensor CM cells were thoroughly intermingled; in the third, the flexor CM cells were preferentially located medially and showed less overlap with the region containing extensor CM cells. C_LIO_LIThese results indicate that each motor cortex site represents a different combination of muscles. The effects evoked from cortical sites separated by several hundred microns invariably involved different profiles of muscle activity. The muscle fields of remote CM cells were rarely identical, while the fields of neighboring CM cells were often similar. Given the number of unrecorded muscles, we conclude that primate motor cortex is a mosaic of output sites representing forelimb muscles in different combinations. C_LI

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Cheney, P. D., Vincent, S. S., Martin, R. F., Fetz, E. E.. 2026-06-30. Spatial Distribution of Cortical Output Zones Affecting Combinations of Forelimb Muscles in the Monkey. https://doi.org/10.64898/2026.06.24.731406

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Cofilin Suppresses Tau-Induced Defects in Dense-Core Granule Formation and Aβ-Induced Neurodegeneration

Intracellular neurofibrillary tangles formed from hyperphosphorylated tau and extracellular amyloid plaques containing aggregated A{beta}-peptides, specific cleavage products of the Amyloid Precursor Protein (APP), are the primary histopathological hallmarks of Alzheimers Disease (AD), the leading cause of dementia in humans. However, the initiating steps that lead to these pathologies and early neurodegeneration, and the mechanisms by which tau- and A{beta}-induced effects might be linked remain unclear. Using the prostate-like secondary cell (SC) in Drosophila, we recently showed that A{beta} modulates normal APP- and membrane-associated protein aggregation in the dense-core granule (DCG) compartments of the regulated secretory pathway by interfering with subsequent membrane:DCG dissociation. This disrupts endolysosomal trafficking and propagates the resulting endolysosomal defects to other cells that endocytose the secreted abnormal DCG proteins. Here we show that overexpressing human tau also disrupts DCG aggregation and membrane:DCG dissociation inside SC secretory compartments, leading to increased endolysosomal targeting of these compartments. In a genetic screen, we find that knockdown of cofilin, which encodes an actin-severing protein required for dynamic remodelling of microfilaments, generates a similar phenotype. Consistent with this, overexpression of Cofilin, which is known to suppress tau-induced neurodegeneration in flies, reduces tau-induced DCG defects in SCs. Indeed, we find that Cofilin overexpression also suppresses A{beta}-induced degeneration in the fly eye. We conclude that membrane:DCG aggregate dissociation in DCG compartments is disrupted by both tau- and A{beta}-induced genetic changes that are relevant to AD, and this partially involves inhibition of actin cytoskeleton dynamics. Increasing actin remodelling activity can suppress neurodegeneration induced by both tau and A{beta}, suggesting that this process provides an important functional link between them that might be targeted therapeutically.

neuroscience↗

Lactate Promotes an Anti-Inflammatory Phenotype in Activated Microglia

Microglial activation is a central component of neuroinflammatory responses in many brain pathologies. Increasing evidence indicates that microglial phenotype is tightly linked to cellular metabolism, with pro-inflammatory activation associated with enhanced glycolytic flux. Lactate, traditionally considered a metabolic substrate, has recently emerged as a signaling molecule capable of modulating immune responses. However, its direct impact on microglial inflammatory activation remains incompletely understood. In the present study, we investigated the effects of lactate on microglial phenotype under inflammatory conditions using primary rat microglial cultures stimulated with lipopolysaccharide (LPS). Microglial activation was assessed through the expression of phenotypic markers, cytokine production, and secreted chemokine profiles. LPS stimulation induced a strong pro-inflammatory response characterized by increased CD86 expression, elevated TNF-alpha secretion, and enhanced release of several pro-inflammatory chemokines. Post-treatment with sodium L-lactate significantly attenuated these inflammatory responses, reducing pro-inflammatory marker expression and cytokine secretion, while restoring the anti-inflammatory marker CD206. To explore the relevance of these findings in a pathological context, the effects of lactate were further examined in a neonatal rat model of hypoxia-ischemia. Sodium L-lactate administration after injury reduced microglial activation and promoted a shift toward an anti-inflammatory phenotype in cortical regions, whereas hippocampal microglia showed a more limited response. Together, these results demonstrate that lactate directly modulates microglial inflammatory activation and cytokine production in vitro and suggest that lactate-mediated metabolic signaling may contribute in vivo to the regulation of neuroinflammatory responses.

neuroscience↗

Different hippocampal subfield volumes predict source memory performance and general cognitive ability in an adult lifespan sample

Modest positive associations between episodic memory performance and whole hippocampal and hippocampal subfield volumes have been reported in numerous prior studies. A smaller number of studies have reported associations between hippocampal volume and performance on tests of non-mnemonic cognition. The present study examined whether these associations were evident in a lifespan sample of cognitively healthy adults. Of particular interest was whether any identified associations were sensitive to age, and whether associations between subfield volumes and mnemonic and non-mnemonic performance were subfield dependent. We acquired high-resolution T1- and T2-weighted structural images from 163 adults (18-87 years of age). Participants also undertook a comprehensive neuropsychological test battery and an in-scanner test of source memory. Principal components analysis was employed to reduce the neuropsychological test scores to 5 cognitive components. Two components reflected memory performance while the other three reflected different aspects of non-mnemonic cognition. Hippocampal subfields (Cornu Ammonis (CA)1, CA2-3, dentate gyrus (DG) and subiculum) were segmented and measured with the Automated Segmentation of Hippocampus Subfields (ASHS) package. Source memory performance was selectively associated across participants with CA2-3 volume. By contrast, both mnemonic and non-mnemonic component scores derived from the test battery were associated exclusively with the volume of the DG. All associations were age-invariant. The findings indicate that different cognitive domains can be dissociated by virtue of their associations with different hippocampal subfields. Of importance, these associations appear to be life-long and hence are unlikely to reflect individual differences in age-related decline in structural integrity.

neuroscience↗