ArticlebioRxiv : the preprint server for biology2026
Gradual consolidation of skilled sequential movements in primary motor cortex of non-human primates.
Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Many of our daily actions rely on skilled sequential movements. Sequence performance improves with practice and can reach expert levels with years of repeated practice, truly exemplifying the saying "Practice makes perfect". Human and non-human primate studies have shown structural and functional changes in the primary motor cortex (M1) following extended practice of sequential movements, suggesting M1's involvement in acquisition and retention of skilled sequences. However, it has been challenging to causally examine M1's role in sequence learning, as inactivation or lesion of M1 impairs movement production. Here, we causally examined M1's contribution to sequence learning by locally inhibiting protein synthesis in M1. Our results show that protein synthesis inhibition in M1 disrupted memory-guided sequential movements at all stages of learning without affecting movement production, though the effects decreased with continued practice. These findings suggest that neural traces for sequential movements are repeatedly consolidated in M1 through protein synthesis, with the rate of consolidation slowing as learning progresses.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.