scholarly journals Abnormal Striatal BOLD Responses to Reward Anticipation and Reward Delivery in ADHD

PLoS ONE ◽  
2014 ◽  
Vol 9 (2) ◽  
pp. e89129 ◽  
Author(s):  
Emi Furukawa ◽  
Patricia Bado ◽  
Gail Tripp ◽  
Paulo Mattos ◽  
Jeff R. Wickens ◽  
...  
2020 ◽  
Author(s):  
Kazuki Shiotani ◽  
Yuta Tanisumi ◽  
Junya Hirokawa ◽  
Yoshio Sakurai ◽  
Hiroyuki Manabe

AbstractOlfactory information directly reaches the amygdala through the olfactory cortex, without the involvement of thalamic areas, unlike other sensory systems. The anterior cortical amygdaloid nucleus (ACo) is one of the olfactory cortices that receives olfactory sensory input, and is part of the olfactory cortical amygdala, which relays olfactory information to the amygdala. To examine its electrophysiological features, we recorded individual ACo neurons during the odor-guided go/no-go task to obtain a water reward. Many ACo neurons exhibited odor-evoked go cue-preferred during the late phase of odor-sampling supporting the population dynamics that differentiate go/no-go responses before executing the odor-evoked behaviors. We observed two types of neurons with different anticipation signals: one neuron type exhibited gradual increases of activity toward reward delivery, while another type exhibited a phasic go cue-preferred activity during odor sampling as well as another phasic anticipatory activity for rewards. These results suggest that the ACo may be involved in reward-related behavioral learning by associating the olfactory information with reward anticipation.


2011 ◽  
Vol 33 (9) ◽  
pp. 2174-2188 ◽  
Author(s):  
James M. Bjork ◽  
Ashley R. Smith ◽  
Gang Chen ◽  
Daniel W. Hommer

PLoS ONE ◽  
2014 ◽  
Vol 9 (2) ◽  
pp. e89954 ◽  
Author(s):  
Mikhail Votinov ◽  
Juergen Pripfl ◽  
Christian Windischberger ◽  
Klaudius Kalcher ◽  
Alexander Zimprich ◽  
...  

2009 ◽  
Vol 102 (4) ◽  
pp. 2526-2537 ◽  
Author(s):  
Sylvie Lardeux ◽  
Remy Pernaud ◽  
Dany Paleressompoulle ◽  
Christelle Baunez

It was recently shown that subthalamic nucleus (STN) lesions affect motivation for food, cocaine, and alcohol, differentially, according to either the nature of the reward or the preference for it. The STN may thus code a reward according to its value. Here, we investigated how the firing of subthalamic neurons is modulated during expectation of a predicted reward between two possibilities (4 or 32% sucrose solution). The firing pattern of neurons responding to predictive cues and to reward delivery indicates that STN neurons can be divided into subpopulations responding specifically to one reward and less or giving no response to the other. In addition, some neurons (“oops” neurons) specifically encode errors as they respond only during error trials. These results reveal that the STN plays a critical role in ascertaining the value of the reward and seems to encode that value differently depending on the magnitude of the reward. These data highlight the importance of the STN in the reward circuitry of the brain.


2018 ◽  
Vol 29 (5) ◽  
pp. 1984-1996 ◽  
Author(s):  
Dardo Tomasi ◽  
Nora D Volkow

Abstract The origin of the “resting-state” brain activity recorded with functional magnetic resonance imaging (fMRI) is still uncertain. Here we provide evidence for the neurovascular origins of the amplitude of the low-frequency fluctuations (ALFF) and the local functional connectivity density (lFCD) by comparing them with task-induced blood-oxygen level dependent (BOLD) responses, which are considered a proxy for neuronal activation. Using fMRI data for 2 different tasks (Relational and Social) collected by the Human Connectome Project in 426 healthy adults, we show that ALFF and lFCD have linear associations with the BOLD response. This association was significantly attenuated by a novel task signal regression (TSR) procedure, indicating that task performance enhances lFCD and ALFF in activated regions. We also show that lFCD predicts BOLD activation patterns, as was recently shown for other functional connectivity metrics, which corroborates that resting functional connectivity architecture impacts brain activation responses. Thus, our findings indicate a common source for BOLD responses, ALFF and lFCD, which is consistent with the neurovascular origin of local hemodynamic synchrony presumably reflecting coordinated fluctuations in neuronal activity. This study also supports the development of task-evoked functional connectivity density mapping.


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