scholarly journals Causal explanation of individual differences in human sensorimotor memory formation

2018 ◽  
Author(s):  
Pierre Petitet ◽  
Jill X. O’Reilly ◽  
Ana M. Gonçalves ◽  
Piergiorgio Salvan ◽  
Shigeru Kitazawa ◽  
...  

AbstractSensorimotor cortex mediates the formation of adaptation memory. Individuals differ in the rate at which they acquire, retain, and generalize adaptation. We present a mechanistic explanation of the neurochemical and computational causes of this variation in humans. Neuroimaging identified structural, functional and neurochemical covariates of a computational parameter that determines memory persistence. To establish causality, we increased sensorimotor cortex excitability during adaptation, using transcranial direct current stimulation. As predicted, this increased retention. Inter-individual variance in the stimulation-induced E:I increase predicted the computational change, which predicted the memory gain. These relations did not hold, and memory was unchanged, with stimulation applied before adaptation. This cognitive state dependent effect was modulated by the BDNF val66met genetic polymorphism. Memory was enhanced by stimulation in Val/Val carriers only, implicating a mechanistic role for activity-dependent BDNF secretion. Sensorimotor cortex E:I causally determines the time constant of memory persistence, explaining phenotypic variation in adaptation decay.

2000 ◽  
Vol 869 (1-2) ◽  
pp. 69-77 ◽  
Author(s):  
Hirofumi Kitagawa ◽  
Yoshihiro Nishimura ◽  
Yuichi Kumazawa ◽  
Takanobu Akamine ◽  
Tetsuro Yamamoto

2020 ◽  
Vol 45 (12) ◽  
pp. 2120-2130 ◽  
Author(s):  
Gonca Bayraktar ◽  
PingAn Yuanxiang ◽  
Alessandro D. Confettura ◽  
Guilherme M. Gomes ◽  
Syed A. Raza ◽  
...  

Abstract DNA methylation is a crucial epigenetic mark for activity-dependent gene expression in neurons. Very little is known about how synaptic signals impact promoter methylation in neuronal nuclei. In this study we show that protein levels of the principal de novo DNA-methyltransferase in neurons, DNMT3A1, are tightly controlled by activation of N-methyl-D-aspartate receptors (NMDAR) containing the GluN2A subunit. Interestingly, synaptic NMDARs drive degradation of the methyltransferase in a neddylation-dependent manner. Inhibition of neddylation, the conjugation of the small ubiquitin-like protein NEDD8 to lysine residues, interrupts degradation of DNMT3A1. This results in deficits in promoter methylation of activity-dependent genes, as well as synaptic plasticity and memory formation. In turn, the underlying molecular pathway is triggered by the induction of synaptic plasticity and in response to object location learning. Collectively, the data show that plasticity-relevant signals from GluN2A-containing NMDARs control activity-dependent DNA-methylation involved in memory formation.


2007 ◽  
Vol 98 (2) ◽  
pp. 878-887 ◽  
Author(s):  
Xiang Yang Chen ◽  
Shreejith Pillai ◽  
Yi Chen ◽  
Yu Wang ◽  
Lu Chen ◽  
...  

Sensorimotor cortex (SMC) modifies spinal cord reflex function throughout life and is essential for operant conditioning of the H-reflex. To further explore this long-term SMC influence over spinal cord function and its possible clinical uses, we assessed the effect of long-term SMC stimulation on the soleus H-reflex. In freely moving rats, the soleus H-reflex was measured 24 h/day for 12 wk. The soleus background EMG and M response associated with H-reflex elicitation were kept stable throughout. SMC stimulation was delivered in a 20-day-on/20-day-off/20-day-on protocol in which a train of biphasic 1-ms pulses at 25 Hz for 1 s was delivered every 10 s for the on-days. The SMC stimulus was automatically adjusted to maintain a constant descending volley. H-reflex size gradually increased during the 20 on-days, stayed high during the 20 off-days, and rose further during the next 20 on-days. In addition, the SMC stimulus needed to maintain a stable descending volley rose steadily over days. It fell during the 20 off-days and rose again when stimulation resumed. These results suggest that SMC stimulation, like H-reflex operant conditioning, induces activity-dependent plasticity in both the brain and the spinal cord and that the plasticity responsible for the H-reflex increase persists longer after the end of SMC stimulation than that underlying the change in the SMC response to stimulation.


2008 ◽  
Vol 86A (2) ◽  
pp. 522-534 ◽  
Author(s):  
Adam W. Feinberg ◽  
Wade R. Wilkerson ◽  
Charles A. Seegert ◽  
Amy L. Gibson ◽  
Leslie Hoipkemeier‐Wilson ◽  
...  

2019 ◽  
Vol 37 (3) ◽  
pp. 234-256 ◽  
Author(s):  
Carly R. Knight ◽  
Isaac Ariail Reed

Mechanisms are ubiquitous in sociological explanation. Recent theoretical work has sought to extend mechanistic explanation further still: into cultural and interpretative analysis. Yet it is not clear that the concept of mechanism can coherently unify interpretation and causal explanation within a single explanatory framework. We note that sociological mechanistic explanation is marked by a crucial disjuncture. Specifically, we identify two conflicting mechanistic approaches: Modular mechanism models depict counterfactual dependence among independent causal chains, whereas meaningful mechanism models depict relational interdependence among semiotic assemblages. This disjuncture, we argue, is grounded in incompatible causal foundations and entails mechanistic models with distinct and conflicting evidentiary standards. We conclude by proposing a way forward: a sociological pluralism that is attentive to the productive incongruity of our distinct explanatory models.


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