Neuronal Activity Related to Anticipated Reward in Frontal Cortex: Does It Represent Value or Reflect Motivation?

2007 ◽  
Vol 1121 (1) ◽  
pp. 431-446 ◽  
Author(s):  
M. R. ROESCH ◽  
C. R. OLSON
Cell Calcium ◽  
2021 ◽  
pp. 102388
Author(s):  
Alex L. Keyes ◽  
Young-cho Kim ◽  
Peter J. Bosch ◽  
Yuriy M. Usachev ◽  
Georgina M. Aldridge

2010 ◽  
Vol 68 ◽  
pp. e265 ◽  
Author(s):  
Yoshihisa Nakayama ◽  
Tomoko Yamagata ◽  
Nariko Arimura ◽  
Jun Tanji ◽  
Eiji Hoshi

1968 ◽  
Vol 12 (5) ◽  
pp. 167-168 ◽  
Author(s):  
Lewis A. Bettinger ◽  
Herman Birch ◽  
Philip M. Groves ◽  
Kathleen S. Mayers ◽  
Richard F. Thompson

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Jelena Scekic-Zahirovic ◽  
Inmaculada Sanjuan-Ruiz ◽  
Vanessa Kan ◽  
Salim Megat ◽  
Pierre De Rossi ◽  
...  

AbstractGene mutations causing cytoplasmic mislocalization of the RNA-binding protein FUS lead to severe forms of amyotrophic lateral sclerosis (ALS). Cytoplasmic accumulation of FUS is also observed in other diseases, with unknown consequences. Here, we show that cytoplasmic mislocalization of FUS drives behavioral abnormalities in knock-in mice, including locomotor hyperactivity and alterations in social interactions, in the absence of widespread neuronal loss. Mechanistically, we identified a progressive increase in neuronal activity in the frontal cortex of Fus knock-in mice in vivo, associated with altered synaptic gene expression. Synaptic ultrastructural and morphological defects were more pronounced in inhibitory than excitatory synapses and associated with increased synaptosomal levels of FUS and its RNA targets. Thus, cytoplasmic FUS triggers synaptic deficits, which is leading to increased neuronal activity in frontal cortex and causing related behavioral phenotypes. These results indicate that FUS mislocalization may trigger deleterious phenotypes beyond motor neuron impairment in ALS, likely relevant also for other neurodegenerative diseases characterized by FUS mislocalization.


1998 ◽  
Vol 80 (5) ◽  
pp. 2671-2687 ◽  
Author(s):  
Kae Nakamura ◽  
Katsuyuki Sakai ◽  
Okihide Hikosaka

Nakamura, Kae, Katsuyuki Sakai, and Okihide Hikosaka. Neuronal activity in medial frontal cortex during learning of sequential procedures. J. Neurophysiol. 80: 2671–2687, 1998. To study the role of medial frontal cortex in learning and memory of sequential procedures, we examined neuronal activity of the presupplementary motor area (pre-SMA) and supplementary motor area (SMA) while monkeys ( n = 2) performed a sequential button press task, “2 × 5 task.” In this paradigm, 2 of 16 (4 × 4 matrix) light-emitting diode buttons (called “set”) were illuminated simultaneously and the monkey had to press them in a predetermined order. A total of five sets (called “hyperset”) was presented in a fixed order for completion of a trial. We examined the neuronal activity of each cell using two kinds of hypersets: new hypersets that the monkey experienced for the first time for which he had to find the correct orders of button presses by trial-and-error and learned hypersets that the monkey had learned with extensive practice ( n = 16 and 10 for each monkey). To investigate whether cells in medial frontal cortex are involved in the acquisition of new sequences or execution of well-learned procedures, we examined three to five new hypersets and three to five learned hypersets for each cell. Among 345 task-related cells, we found 78 cells that were more active during performance of new hypersets than learned hypersets (new-preferring cells) and 18 cells that were more active for learned hypersets (learned-preferring cells). Among new-preferring cells, 33 cells showed a learning-dependent decrease of cell activity: their activity was highest at the beginning of learning and decreased as the animal acquired the correct response for each set with increasing reliability. In contrast, 11 learned-preferring cells showed a learning-dependent increase of neuronal activity. We found a difference in the anatomic distribution of new-preferring cells. The proportion of new-preferring cells was greater in the rostral part of the medial frontal cortex, corresponding to the pre-SMA, than the posterior part, the SMA. There was some trend that learned-preferring cells were more abundant in the SMA. These results suggest that the pre-SMA, rather than SMA, is more involved in the acquisition of new sequential procedures.


2012 ◽  
Vol 56 (1) ◽  
pp. 103-107 ◽  
Author(s):  
Aleksandra Krawczyk ◽  
Radosław Szalak ◽  
Jadwiga Jaworska-Adamu

Abstract The aim of the study was to define morphology and distribution of calretinin (CR) positive neurons in the frontal cortex of adult chinchilla males and intracellular localisation of the protein in this area. The brains of 5 adult chinchilla males were used in the study. CR immunoreactive neurons were shown with peroxidase-antiperoxidase immunohistochemical reaction using a specific monoclonal antibody. Intensive CR immunoreactivity was demonstrated mainly in few polymorphic neurons of II, III, and V layers. Cytoplasmic and nuclear reaction product in most CR positive neurons was diffuse and in some neurons of layer V in the form of granules localised peripherally. In a few cells more intensive staining was observed in the nuclei than in the cytoplasm. The results indicate the presence of heteromorphic CR positive neurons in specific layers of the frontal cortex. Nuclear localisation of CR in neurons suggests passive transport of this protein, which may affect the nuclear genes. This protein is a neuroprotector maintaining appropriate level of calcium, modulating neuronal activity, and synaptic conduction in the frontal cortex of chinchilla.


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