The Duration of the Movement Aftereffect as an Index of Psychiatric Illness

Perception ◽  
1994 ◽  
Vol 23 (10) ◽  
pp. 1145-1153 ◽  
Author(s):  
John Harris

The duration of the movement aftereffect (MAE) has sometimes been used to make inferences about the subject's state (for example, their level of arousal). Some studies are reviewed in which visual aftereffects (including the MAE) were measured in schizophrenia, with inconsistent results. Some relevant psychopharmacological and neurological evidence is considered. It is concluded that: (i) Differences in the clinical status of the schizophrenic subjects and whether they were receiving medication, but not the method used to measure aftereffects, may underlie the interstudy disagreements. (ii) The effect of schizophrenia is to increase MAE duration, and this is not due to some peripheral artefact. (iii) Longer MAEs in the illness could result from enhanced neurally signalled contrast and/or from the increased adaptability of cortical neurons.

2021 ◽  
Author(s):  
Stephanie Cerceo Page ◽  
Srinidhi Rao Sripathy ◽  
Federica Farinelli ◽  
Zengyou Ye ◽  
Yanhong Wang ◽  
...  

Neurons derived from human induced pluripotent stem cells (hiPSCs) have been used to model basic cellular aspects of neuropsychiatric disorders, but the relationship between the emergent phenotypes and the clinical characteristics of donor individuals has been unclear. We analyzed RNA expression and indices of cellular function in hiPSC-derived neural progenitors and cortical neurons generated from 13 individuals with high polygenic risk scores (PRS) for schizophrenia and a clinical diagnosis of schizophrenia, along with 15 neurotypical individuals with low PRS. We identified electrophysiological measures associated with diagnosis that implicated altered Na+ channel function and GABA-ergic neurotransmission. Importantly, electrophysiological measures predicted cardinal clinical and cognitive features found in these schizophrenia patients. The identification of basic neuronal physiological properties related to core clinical characteristics of illness may prove useful in generating leads that enable development of novel therapeutics.


2022 ◽  
Vol 119 (3) ◽  
pp. e2109395119
Author(s):  
Stephanie Cerceo Page ◽  
Srinidhi Rao Sripathy ◽  
Federica Farinelli ◽  
Zengyou Ye ◽  
Yanhong Wang ◽  
...  

Neurons derived from human induced pluripotent stem cells (hiPSCs) have been used to model basic cellular aspects of neuropsychiatric disorders, but the relationship between the emergent phenotypes and the clinical characteristics of donor individuals has been unclear. We analyzed RNA expression and indices of cellular function in hiPSC-derived neural progenitors and cortical neurons generated from 13 individuals with high polygenic risk scores (PRSs) for schizophrenia (SCZ) and a clinical diagnosis of SCZ, along with 15 neurotypical individuals with low PRS. We identified electrophysiological measures in the patient-derived neurons that implicated altered Na+ channel function, action potential interspike interval, and gamma-aminobutyric acid–ergic neurotransmission. Importantly, electrophysiological measures predicted cardinal clinical and cognitive features found in these SCZ patients. The identification of basic neuronal physiological properties related to core clinical characteristics of illness is a potentially critical step in generating leads for novel therapeutics.


1983 ◽  
Vol 28 (3) ◽  
pp. 243-243
Author(s):  
Samuel Pieper
Keyword(s):  

Author(s):  
Alexi Nott ◽  
James D. Robinson ◽  
Antonella Riccio

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