Neural basis of utility estimation
References (76)
Pleasure: the common currency
J Theor Biol
(1992)- et al.
Task difficulty increases thresholds of rewarding brain stimulation
Behav Brain Rev
(1990) - et al.
Analysis of the relationships between self-stimulation sniffing and brain-stimulation sniffing
Physiol Behav
(1992) - et al.
Chronic food restriction and weight loss produce opioid facilitation of perifornical hypothalamic self-stimulation
Brin Res
(1993) - et al.
On the neural computation of utility
Curr Dir Psychol Sci
(1996) - et al.
A portrait of the substrate for self-stimulation
Psychol Rev
(1981) - et al.
Choice as time allocation
J Exp Anal Behav
(1969) - et al.
Electrical stimulation of the rat diencephalon: differential effects of interrupted stimulation on on- and off-responding
Brain Res
(1977) - et al.
Self-control choice with electrical stimulation of the brain
Behav Processes
(1987) - et al.
Economic substitutability of electrical brain stimulation, food, and water
J Exp Anal Behav
(1991)
Substitutability in time allocation
Psychol Rev
Addictive drugs and brain stimulation reward
Annu Rev Neurosci
Behaviorally derived measures of conduction velocity in the substrate for rewarding medial forebrain bundle stimulation
Brain Res
Behavioral methods for inferring anatomical linkage between rewarding brain stimulation sites
J Comp Physiol Psychol
Effects of excitotoxic lesions of the basal forebrain on MFB self-stimulation
Physiol Behav
Increased ipsilateral expression of Fos following lateral hypothalamic self-stimulation
Brain Res
Fos-like immunoreactivity in forebrain regions following self-stimulation of the lateral hypothalamus and the ventral tegmental area
Behav Brain Res
Physiological measures of conduction velocity and refractory period for putative reward-relevant MFB axons arising in the rostral MFB
Physiol Behav
Interhemispheric links in brain stimulation reward
Behav Brain Res
Electrically evoked behaviors: axons and synapses mapped with collision tests
Behav Brain Res
Excitability properties of medial forebrain bundle axons of A9 and A10 dopamine cells
Brain Res
Action of drugs of abuse on brain reward systems
Pharmacol Biochem Behav
The role of the dopaminergic projections in MFB self-stimulation
Behav Brain Res
Differential effects of atropine, procaine and dopamine in the rat ventral tegmentum on lateral hypothalamic rewarding brain stimulation
Behav Brain Res
Competition and summation between rewarding effect of sucrose and lateral hypothalamic stimulation in the rat
Behav Neurosci
Effects of sodium depletion on competition and summation between rewarding effects of salt and lateral hypothalamic stimulation in the rat
Behav Neurosci
Differential effects of postingestive feedback on the reward value of sucrose and lateral hypothalamic stimulation in the rat
Behav Nuerosci
Administration of ovarian steroid hormones does not change the reward effectiveness of lateral hypothalamic stimulation in ovariectomized rats
Psychobiology
The effects of gonadal steroids on brain stimulation reward in female rats
Behav Brain Res
Curve-shift analysis of self-stimulation in food-restricted rats: relationships between daily meal, plasma corticosterone and reward sensitization
Brain Res
Saturation of subjective reward magnitude as a function of current and pulse frequency
Behav Neurosci
Reinforcer magnitude (sucrose concentration) and the matching law theory of response strength
J Exp Anal Behav
Reward, performance, and the response strength method in self-stimulating rats: validation and neuroleptics
Physiol Behav
Relative and absolute strength of response as a function of frequency of reinforcement
J Exp Anal Behav
On the law of effect
J Exp Anal Behav
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2020, Neuroscience and Biobehavioral ReviewsValence processing differs across stimulus modalities
2018, NeuroImageCitation Excerpt :It has been suggested that the medial orbitofrontal cortex (OFC) – the most ventral part of the mPFC – integrates multimodal sensory information and is the most likely area in the brain to mediate valence processing for stimuli originating from different sensory modalities (Kringelbach, 2005). This idea of a common neuronal brain region or network for neuronal processing of valence across stimulus modalities is shared by Montague & Berns' predictor-valuation model (Montague and Berns, 2002) and Shizgal’ utility estimation model (Shizgal, 1997). These models argue that the value of multimodal stimuli is converted into a common scale (or currency) allowing the organism to compare their value or ‘utility’ to guide future behaviors (Grabenhorst et al., 2010; Montague and Berns, 2002).
It's all in the type of the task: Dopamine modulates kinematic patterns during competitive vs. cooperative interaction in Parkinson's disease
2016, NeuropsychologiaCitation Excerpt :As postulated by some, engagement in social interaction and rewards processing require basal ganglia (BG) involvement (Izuma et al., 2008; Spreckelmeyer et al., 2009; Lebreton et al., 2009; Pfeiffer et al., 2014), and dopamine neurons play a central role in the reward circuit (Schultz, 2002; Wise, 2002). Behavioral and pharmacological studies on dopamine pathways have described associations between the mesolimbic and nigrostriatal pathways and reward and motor activity (Koob and Le Moal, 1997; Panksepp, 1998; Phillips et al., 1992; Shizgal, 1997; Wise, 2004). Much of the causal evidence supporting the hypothesis that the dopamine mediates the brain reward system is based on studies examining the pharmacological blockade of dopamine receptors in animals.
Toward a systems-oriented approach to the role of the extended amygdala in adaptive responding
2016, Neuroscience and Biobehavioral ReviewsThe neural substrates for the rewarding and dopamine-releasing effects of medial forebrain bundle stimulation have partially discrepant frequency responses
2016, Behavioural Brain ResearchCitation Excerpt :For example, dopamine receptor antagonists block or reduce ICSS whereas indirect dopamine agonists, such as amphetamine and cocaine, potentiate ICSS [14,15]. However, behavioral studies also implicate neurons with highly excitable, myelinated axons in the rewarding effect of MFB stimulation [16–20,6], and electrophysiological studies have identified non-dopaminergic neurons, directly driven by MFB stimulation, that have characteristics consistent with those inferred from the behavioral studies [21–23]. Fast-scan cyclic voltammetry (FSCV) confirms that midbrain dopamine neurons are activated trans-synaptically by rewarding MFB stimulation.